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. 2017 Dec 6;27:138–150. doi: 10.1016/j.ebiom.2017.11.029

Mice with an Oncogenic HRAS Mutation are Resistant to High-Fat Diet-Induced Obesity and Exhibit Impaired Hepatic Energy Homeostasis

Daiju Oba a, Shin-ichi Inoue a,⁎⁎, Sachiko Miyagawa-Tomita b,c,d, Yasumi Nakashima e, Tetsuya Niihori a, Seiji Yamaguchi f, Yoichi Matsubara a,g, Yoko Aoki a,⁎,1
PMCID: PMC5828294  PMID: 29254681

Abstract

Costello syndrome is a “RASopathy” that is characterized by growth retardation, dysmorphic facial appearance, hypertrophic cardiomyopathy and tumor predisposition. > 80% of patients with Costello syndrome harbor a heterozygous germline G12S mutation in HRAS. Altered metabolic regulation has been suspected because patients with Costello syndrome exhibit hypoketotic hypoglycemia and increased resting energy expenditure, and their growth is severely retarded. To examine the mechanisms of energy reprogramming by HRAS activation in vivo, we generated knock-in mice expressing a heterozygous Hras G12S mutation (HrasG12S/+ mice) as a mouse model of Costello syndrome. On a high-fat diet, HrasG12S/+ mice developed a lean phenotype with microvesicular hepatic steatosis, resulting in early death compared with wild-type mice. Under starvation conditions, hypoketosis and elevated blood levels of long-chain fatty acylcarnitines were observed, suggesting impaired mitochondrial fatty acid oxidation. Our findings suggest that the oncogenic Hras mutation modulates energy homeostasis in vivo.

Keywords: Costello syndrome, Hras G12S, Mitochondrial fatty acid oxidation, Diet-induced obesity, Cancer metabolism, ERK

Highlights

  • •

    Mice expressing Hras G12S (HrasG12S/+) showed Costello syndrome-like phenotypes, including craniofacial and cardiac defects.

  • •

    HrasG12S/+ mice are resistant to high-fat diet (HFD)-induced obesity, showing microvesicular hepatic steatosis.

  • •

    Upon fasting, HFD-fed HrasG12S/+ mice show abnormal hepatic fatty acid oxidation, hypoketosis and early hypoglycemia.

Costello syndrome is a congenital anomaly syndrome, which is caused by germline mutations in HRAS oncogene. Altered metabolic regulation has been suspected because patients with Costello syndrome exhibit hypoketotic hypoglycemia and increased resting energy expenditure, and growth retardation. Here, we generated a mouse model for Costello syndrome expressing a Hras G12S mutation, which showed craniofacial and heart abnormalities. On a high-fat diet, mutant mice exhibited a lean phenotype with poor weight gain and microvesicular hepatic steatosis. Under starvation conditions, impaired mitochondrial fatty acid oxidation has been observed. These results suggest that oncogenic RAS signaling in mice modulates energy homeostasis in vivo.

1. Introduction

Costello syndrome is a rare disorder with multiple congenital anomalies that is characterized by intellectual disability, high birth weight, postnatal growth retardation with feeding difficulties, curly hair, relative macrocephaly, dysmorphic facial features, loose skin, hypertrophic cardiomyopathy and a predisposition to malignancies (Costello, 1977, Hennekam, 2003). In 2005, we discovered that germline mutations in Harvey rat sarcoma viral oncogene homolog (HRAS) cause Costello syndrome (Aoki et al., 2005). Approximately 80% of patients with Costello syndrome have germline mutations in HRAS, which is one of the components of the RAS-MAPK signaling pathway (Aoki et al., 2005, Gripp et al., 2006, Kerr et al., 2006). Disorders resulting from germline mutations in components of the RAS-MAPK signaling pathway are now collectively referred to as RASopathies or RAS-MAPK syndromes, including Noonan syndrome, Costello syndrome, cardio-facio-cutaneous (CFC) syndrome, Noonan syndrome with multiple lentigines (LEOPARD syndrome) and neurofibromatosis type 1 (Aoki et al., 2016, Aoki et al., 2008, Rauen, 2013, Tidyman and Rauen, 2009).

Somatic HRAS mutations at residues 12, 13 and 61 are frequently found in bladder cancer, head and neck cancer, vulvar and cutaneous squamous cell carcinoma and lung cancer (Lawrence et al., 2014, McDaniel et al., 2014, Oliva et al., 2004, Trietsch et al., 2014; COSMIC database http://cancer.sanger.ac.uk/cosmic/gene/analysis?ln=HRAS). The most common somatic mutation at codon 12 of HRAS is the G12V mutation, c.35G > T (p.Gly12Val). In contrast, the most frequent germline mutation in Costello syndrome patients (> 80%) is the HRAS G12S mutation, c.34G > A (p.Gly12Ser) (Aoki et al., 2005, Gripp et al., 2006, Kerr et al., 2006). It has been reported that the levels of the GTP-bound active form of HRAS G12V are higher than those of HRAS G12S (Wey et al., 2013). Two groups have developed Costello syndrome mouse models that express Hras G12V (HrasG12V knock-in mice). However, mice with the Hras G12S mutation, which is the most common mutation in Costello syndrome, have not been generated.

Costello syndrome patients with germline HRAS mutations exhibit fasting hypoglycemia with growth hormone and cortisol deficiencies, and hypoglycemia with or without decreased ketone bodies (Hennekam, 2003). Moreover, patients with Costello syndrome have resting energy expenditure, which indicates enhanced basal metabolism (Leoni et al., 2016). Recent studies have provided evidence that patients with RASopathies and associated mouse models exhibit mitochondrial dysfunction, including morphological defects, oxidative phosphorylation disorders and enzyme deficiencies in the oxidative phosphorylation system (Aeby et al., 2007, Kleefstra et al., 2011, Moriya et al., 2015). However, the metabolic homeostasis of individuals with oncogenic germline mutations (RASopathies) remains unclear. Recent studies have shown that cancer cells with RAS mutations exhibit altered metabolism characterized by enhanced glucose uptake, glycolysis, lipid synthesis and glutamine catabolism (Bryant et al., 2014, Zheng et al., 2015, Zhou et al., 2016). To gain an understanding of the effects of RAS activation on energy homeostasis in vivo, we generated knock-in mice expressing the Costello syndrome-associated Hras G12S mutation and examined energy homoeostasis in the liver.

2. Material and Methods

2.1. Generation of HrasG12S Knock-in Mice

Two BAC clones containing the Hras gene, ID: RP23-210J2 and RP-23-112C12, were used to generate the targeting vector. To construct the targeting vector for HrasG12S knock-in mice, DNA fragments including Hras exon 0, loxp-SA-Exon 1, Hras cDNA (Exon1–4)-polyA and SA-Exon1–4 were amplified using mouse BAC clones. These DNA fragments were ligated into the pBSIISK + or pBS vector. The Hras G12S (exon 1) mutation was introduced using site-directed mutagenesis. For construct 1, the loxp-SA-Exon 1 regions were inserted into the pBS vector containing Hras cDNA (Exon1–4)-poly A. For construct 2, the FRT-Neo-FRT-loxp cassettes and construct 1 fragments were inserted into the pBSIISK + vector containing Hras exon 0 DNA fragments. For the targeting vector, the construct 2 fragments were inserted into the pBSIISK + vector containing SA-Exon1–4 regions. The targeting vector was linearized with SalI and electroporated into the C57B6-derived BRUCE-4 ES cells. We used genotyping and sequencing and tested the Cre-mediated recombination system to confirm the correctly targeted ES clones. Furthermore, homologous recombination was confirmed by Southern blotting using 5′, 3′ and Neo probes. The probe sequences are shown in Supplementary Table 1. Screened ES clones were then microinjected into BALB/c blastocysts, and the resulting chimeras were crossed with C57BL/6J mice to obtain HrasG12S Neo/+ heterozygous mice. Excisions of the SA-Hras cDNA-poly A and Neo cassette were achieved by crossing the HrasG12S Neo/+ heterozygotes with CAGCre transgenic mice on the C57BL/6J background (RIKEN BioResource Center, Tsukuba, Japan; RBRC01828) (Matsumura et al., 2004). To generate the HrasG12S/+ mice, the HrasG12S/+;Cre mice were crossed with C57BL/6 J mice (Charles River Laboratories Japan, Yokohama, Japan). All animal experiments were approved by the Animal Care and Use Committee of Tohoku University.

2.2. Genotyping

Genomic DNA was purified from mouse tail tissue using the Maxwell 16 Mouse Tail DNA Purification Kit (Promega, Madison, WI). Genotyping of Hras+/+ and HrasG12S/+ alleles was carried out by PCR amplification using KOD Fx Neo (TOYOBO, Osaka, Japan). The primers used for PCR were 5’-CGCTCAGTAAATAGTTGTAGGTTGC-3′ and 3′- CTCAGACCAGAGAATCCACAGAAC-5′.

2.3. Mouse Feeding and Care

The female mice were housed in a temperature-controlled room with a 12-h light/dark cycle and fed a conventional laboratory diet (control diet (CD); Labo MR Stock, Nosan Corporation Life-Tech Department, Yokohama, Japan) before weaning at 5 weeks of age. After weaning, the mice were fed a HFD containing 60% fat (HFD-60; Oriental Yeast Corporation, Tokyo, Japan) and housed in individual cages. The compositions of the Labo MR Stock and HFD-60 are shown in Supplementary Tables 2 and 3. Body weight and food intake were measured every 7 days.

2.4. Analysis of Serum Parameters

Mice were fed a HFD from 5 to 16 weeks of age. Serum samples from 16-week-old mice were obtained from the inferior vena cava while the mice were under anesthesia. The fasted blood samples were obtained after 24 h of fasting. All parameters were measured at the Oriental Yeast Corporation Nagahama Laboratory, Nagahama, Japan.

2.5. Measurement of Lipid Content

Liver and fecal samples were obtained from mice fed a HFD from 5 to 16 weeks of age. Total lipid extraction was performed by the Folch extraction procedure (Folch et al., 1957). The content of triglyceride, total cholesterol and free fatty acid were measured by using Triglyceride E-test Wako, Cholesterol E-test Wako and NEFA C-test Wako (Wako Pure Chemical Industries, Osaka, Japan), respectively.

2.6. Glucose and β-Hydroxybutyric Acid Measurement

Mice were fed a HFD from 5 to 16 weeks of age before the fasting test. Blood glucose and β-hydroxybutyric acid levels were measured after 0, 24 and 48 h of fasting. Samples were obtained from the tail veins of anesthetized mice and analyzed using a FreeStyle Precision Neo (Abbott Laboratories, Chicago, IL).

2.7. Blood Acylcarnitine Profiling

Mice were fed a HFD from 5 to 22–27 weeks of age. Blood samples were obtained from tail vein after 24 h of fasting and spotted on filter paper. The samples were prepared as previously described (Kobayashi et al., 2007). Blood acylcarnitine was measured using an API 3000 triple quadrupole tandem mass spectrometer along with a SIL-HTc autosampler (Shimadzu, Kyoto, Japan) and analyzed using ChemoView™ software (Applied Biosystems/MDS SCIEX, Toronto, Canada).

2.8. Urinary β-Hydroxybutyric Acid and Pyruvic Acid Measurement

Mice were fed a HFD from 5 to 22–27 weeks of age. Urine samples were blotted to filter paper then dried at room temperature. β-hydroxybutyric acid and pyruvic acid were measured by GC/MS. The procedures of sample preparation and measurement were as previously described (Fu et al., 2000, Kimura et al., 1999).

2.9. Histology and Immunohistochemistry

Tissues were fixed in 10% neutral buffered formalin and then embedded in paraffin. The sections were stained with hematoxylin and eosin (HE), periodic acid-Schiff (PAS) or picrosirius red. To measure the cross-sectional areas of the cardiomyocytes, the sections were stained with fluorescein isothiocyanate-labeled wheat germ agglutinin (FITC-WGA, L4895; Sigma-Aldrich, St Louis, MO) for 1 h at room temperature. The slides were mounted using the ProLong Gold antifade reagent with 4′,6-diamidino-2-phenylindole. The areas of the cardiomyocytes with nuclei were measured using ImageJ software (http://rsbweb.nih.gov/ij/).

2.10. Quantitative RT-PCR

Total RNA extraction and cDNA synthesis were performed as previously described (Inoue et al., 2014). Quantitative PCR analysis was performed using the Universal Probe Library (Roche Life Science, Basel, Switzerland) with StepOnePlus (Thermo Fisher Scientific). Amplification primers and hydrolysis probes are described in Supplementary Table 4.

2.11. Western Blotting

Liver tissues were homogenized in lysis buffer (10 mM Tris-HCL, pH 8.0 and 1% SDS) containing phosphatase and protease inhibitor cocktails (P5726 and P8340, respectively; Sigma-Aldrich). These lysates were centrifuged at 15,000 rpm for 30 min at 20° C, and the protein concentration was determined using the Bradford method with the Bio-Rad Protein Assay (Bio-Rad Laboratories, Hercules, CA). The lysates were subjected to SDS-PAGE electrophoresis (4–20% Criterion TGX Precast Gels; Bio-Rad Laboratories) and transferred to either a nitrocellulose or PVDF membrane (Trans-Blot Turbo Transfer pack; Bio-Rad Laboratories) using the Trans-Blot Turbo Transfer System (Bio-Rad Laboratories). After blocking with 5% non-fat milk, the membranes were incubated overnight at 4° C with following antibodies (the catalog numbers are in parentheses). H-Ras (sc-520) and AMPKα 1/2 (sc-25,792) from Santa Cruz Biotechnology (Santa Cruz, CA) and ERK1/2 (9102), phospho-ERK1/2 (9101), AKT (9272), phospho-AKT (on Ser473; 9018), phospho-AMPKα (on Thr172; 2535) from Cell Signaling (Danvers, MA). All of the membranes were visualized using the Western Lightning ECL-Plus Kit (PerkinElmer, Waltham, MA). The band intensities were quantified using ImageJ software.

2.12. Intraperitoneal Glucose Tolerance Test (IPGTT)

Mice were fed a HFD from 5 to 16 weeks of age before IPGTT. 2 g/kg body weight of glucose was injected intraperitoneally in mice after 6 h fasting. Blood glucose levels were measured before glucose injection and after 30, 60, 90 and 120 min of glucose injection. Samples were obtained from the tail veins of anesthetized mice and analyzed using a FreeStyle Precision Neo (Abbott Laboratories).

2.13. Statistical Analysis

The data are presented as the mean ± standard deviation (SD). The Mann-Whitney U-test and Welch's t-test were used for comparisons of two groups, and Tukey's test was used for multiple comparisons. The log-rank test was used for the survival curve, which was constructed using the Kaplan-Meier method. All data were analyzed using JMP Pro12 software (SAS, Cary, NC), and p < 0.05 was considered statistically significant.

3. Results

3.1. Generation of Hras G12S Knock-in Mice

To generate Hras G12S knock-in mice, a targeting vector with a GGA (Gly) to AGC (Ser) mutation in codon 12 (Fig. 1a) was electroporated into C57B6-derived ES cells. The targeted clones were confirmed by Southern blotting (data not shown). Screened ES cells were microinjected into BALB/c blastocysts. To obtain HrasG12S/+;Cre mice, the chimeras (HrasG12S Neo/+ mice) were crossed with CAG-Cre transgenic mice. Male HrasG12S/+;Cre mice were crossed with female C57BL/6J mice to remove Cre, and the genotype was confirmed by PCR (Supplementary Fig. 1). HrasG12S/+ mice were present at the expected Mendelian ratios at weaning and were fertile. In contrast, all of the homozygous Hras G12S knock-in mice died during the prenatal period (data not shown).

Fig. 1.

Fig. 1

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Generation of Hras G12S knock-in mice and the Hras+/+ and HrasG12S/+ mouse phenotypes.

(a) Gene-targeting strategy to generate the HrasG12S/+ knock-in mice. Exons (solid boxes), neomycin cassettes (hexagonal boxes), Hras cDNA (Exons 1–4)-poly A cassettes (open boxes), splice acceptor sites (SA, labeled gray boxes), loxP sites (open arrowheads) and Flp recombination target (FRT) sites (solid arrowheads) are indicated. The SA-HRAS cDNA-poly A and Neo cassettes were removed by crossing with CAG-Cre transgenic mice. (b, c, d) Representative facial appearance, tooth arrangement and anal images of Hras+/+ and HrasG12S/+ mice. (b) The panels indicate the round facial appearance (upper panel) and shortened nasal bridge (lower panel) in HrasG12S/+ mice compared with Hras+/+ mice. (c) Malocclusion in HrasG12S/+ mice. (d) Rectal prolapse in HrasG12S/+ mice. (e) Body weights of male (upper graph) and female (lower graph) Hras+/+ and HrasG12S/+ mice fed a control diet (CD). The data are presented as the mean ± SD (Hras+/+ (n = 17) and HrasG12S/+ (n = 16) for males; Hras+/+ (n = 17) and HrasG12S/+ (n = 18) for females). *p < 0.05, **p < 0.01 (Welch's t-test) compared with Hras+/+ mice. (f) Gross morphology of hearts from Hras+/+ and HrasG12S/+ mice at 1 year of age. The lower bar graph shows the heart weight (HW) to body weight (BW) ratios of Hras+/+ and HrasG12S/+ mice at 16 weeks and 1 year of age. The data are expressed as the mean ± SD (Hras+/+ (n = 8) and HrasG12S/+ (n = 8) at 16 weeks of age; Hras+/+ (n = 10) and HrasG12S/+ (n = 7) at 1 year of age). *p < 0.05, **p < 0.01 (Welch's t-test) compared with Hras+/+ mice. Scale bar = 5 mm. (g) Transverse sections of wheat germ agglutinin-stained hearts from Hras+/+ and HrasG12S/+ mice at 16 weeks and 1 year of age. The lower bar graph shows the average area of left ventricular (LV) cardiomyocytes in Hras+/+ and HrasG12S/+ mice at 16 weeks and 1 year of age. The data are expressed as the mean ± SD (Hras+/+ (n = 5) and HrasG12S/+ (n = 7) at 16 weeks of age; Hras+/+ (n = 5) and HrasG12S/+ (n = 7) at 1 year of age). **p < 0.01 (Tukey's test) compared with Hras+/+ mice at 16 weeks and 1 year of age. ##p < 0.01 (Tukey's test) compared with HrasG12S/+ mice at 16 weeks of age. Scale bar = 50 μm. (h) Gross morphology of kidneys from Hras+/+ and HrasG12S/+ mice at 1 year of age. The bar graph indicates the kidney weight (KW) to body weight (BW) ratios of Hras+/+ and HrasG12S/+ mice at 16 weeks and 1 year of age. The data are expressed as the mean ± SD (Hras+/+ (n = 8) and HrasG12S/+ (n = 8) at 16 weeks of age; Hras+/+ (n = 10) and HrasG12S/+ (n = 7) at 1 year of age). **p < 0.01 (Welch's t-test) compared with Hras+/+ mice. Scale bar = 5 mm. (i and j) Coronal sections of kidneys from Hras+/+ and HrasG12S/+ mice at 1 year of age stained with HE, PAS and Sirius red. Scale bar = 100 μm. (j) The box plot shows the proportion of fibrosis area in Sirius red-stained sections (Hras+/+ (n = 9) and HrasG12S/+ (n = 8)). The open circle (○) indicates an outlier. *p < 0.05 (Mann-Whitney U test) compared with Hras+/+ mice. (K) Gross morphology of a cystic kidney from a HrasG12S/+ mouse at 16 weeks of age.

3.2. HrasG12S/+ Mice Exhibit Facial Dysmorphia, Growth Alterations, Cardiomyocyte Hypertrophy and Kidney Anomalies

Patients with Costello syndrome have postnatal onset of growth deficiency associated with feeding difficulty; several facial features, including macrocephaly with a prominent forehead, low-set ears with thick lobes, strabismus, a depressed nasal bridge, thick lips, curly hair and dental anomalies; cardiac anomalies; skin anomalies and renal anomalies (Hennekam, 2003, Myers et al., 2014, Takahashi and Ohashi, 2013). All HrasG12S/+ mice exhibited dysmorphic facial features, including a round head and a shortened nasal bridge (Fig. 1b). These facial features were reminiscent of the Hras G12V knock-in mouse (Chen et al., 2009, Schuhmacher et al., 2008). In addition, malocclusion and rectal prolapse were observed in HrasG12S/+ mice (Fig. 1c and d; Supplementary Table 5). Skin anomalies and curly hair were not observed in HrasG12S/+ mice. Both male and female 5-week-old HrasG12S/+ mice displayed significant growth retardation, although the body weights of these mice normalized by 6 weeks of age (Fig. 1e). Thereafter, the female, but not male, HrasG12S/+ mice displayed significant overgrowth after 9 weeks of age compared with Hras+/+ mice (Fig. 1e).

The representative cardiac anomalies in Costello syndrome are arrhythmia, hypertrophic cardiomyopathy, atrial septal defects and ventricular septal defects (Hennekam, 2003). HrasG12S/+ mice had cardiomegaly, which was characterized by a significantly increased heart weight (HW) to body weight (BW) ratio compared with Hras+/+ mice (Fig. 1f). Morphometric analysis of left ventricular (LV) cardiomyocytes indicated that these cells were significantly larger in HrasG12S/+ mice than in Hras+/+ mice; this cellular enlargement progressed over time but did not result in the development of cardiac fibrosis (Fig. 1g and Supplementary Fig. 2). At 1 year of age, electrocardiographic analysis revealed significantly deep S waves, low T waves and a short PR interval in HrasG12S/+ mice compared with Hras+/+ mice (Supplementary Table 6). Despite the cardiomegaly and cardiomyocyte hypertrophy, there were no significant changes in intraventricular septum thickness or left ventricular systolic function, including ejection fraction and fractional shortening on echocardiograms, in HrasG12S/+ mice compared with Hras+/+ mice at 1 year of age. These results suggest that there were no significant changes in cardiac function (Supplementary Table 7). Furthermore, the heart structure of HrasG12S/+ mice appeared normal in the echocardiographic and histological analyses, suggesting that there were no atrial septal defects or ventricular septal defects (data not shown). A significantly increased kidney weight (KW) to BW ratio, mesangial proliferation and kidney fibrosis indicated renal enlargement in HrasG12S/+ mice at 1 year of age (Fig. 1h-1j) but not at 16 weeks of age (data not shown). Furthermore, 4.6% of the HrasG12S/+ mice had a unilateral cystic kidney (Fig. 1k; Supplementary Table 5). These observations indicate that HrasG12S/+ mice have dysmorphic facial features, overgrowth (in females), cardiomegaly with cardiomyocyte hypertrophy and kidney anomalies.

3.3. HrasG12S/+ Mice Are Resistant to HFD-Induced Weight Gain

Because we did not observe any differences in body weight between Hras+/+ and HrasG12S/+ mice on a normal diet, we used a model of HFD-induced obesity to explore the metabolic status of HrasG12S/+ mice. Male HrasG12S/+ mice were significantly lighter than Hras+/+ mice after 13 weeks of age with HFD feeding. In female mice, there were no differences in body weight between Hras+/+ and HrasG12S/+ mice from 14 to 23 weeks of age. After 24 weeks of age, HrasG12S/+ mice were significantly lighter than Hras+/+ mice (Fig. 2a and b). Food intake from birth to 11 weeks was comparable between Hras+/+ and HrasG12S/+ mice, except during the third and fifth weeks of HFD feeding (Fig. 2c); during these weeks, food intake by HrasG12S/+ mice was significantly higher than that by Hras+/+ mice (Fig. 2c). The average weight gain of HrasG12S/+ mice was significantly lower than that of Hras+/+ mice after 8 weeks but not after 9 weeks, despite the increased or comparable levels of food intake by HrasG12S/+ mice (Fig. 2d). Furthermore, there was less inguinal white adipose tissues in HrasG12S/+ mice at both 16 weeks and 1 year of age compared with Hras+/+ mice (Fig. 2e). A dramatic increase in mortality was observed among HrasG12S/+ mice fed a HFD compared with HrasG12S/+ mice fed a CD, whereas HrasG12S/+ mice were resistant to HFD-induced obesity (Fig. 2f). Consistent with the increased mortality of HFD-fed HrasG12S/+ mice, HrasG12S/+ mice developed progressive cardiomyocyte hypertrophy and kidney injury (Supplementary Fig. 3). Furthermore, the HrasG12S/+ mice that died at 60 weeks of age had developed the aging phenotype, including hair loss, kyphosis and cutaneous lesions due to scratching (data not shown). These phenotypes, including increased mortality, cardiomyocyte hypertrophy and kidney injury, were more pronounced in female HrasG12S/+ mice than in male HrasG12S/+ mice (data not shown). Thus, a subsequent study was performed using female HrasG12S/+ mice.

Fig. 2.

Fig. 2

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Resistance to HFD-induced obesity in HrasG12S/+ mice.

(a) Representative appearance of Hras+/+ and HrasG12S/+ mice fed a HFD at 16 weeks and 1 year of age. (b) Body weights of Hras+/+ and HrasG12S/+ mice fed a HFD. The data are expressed as the mean ± SD (Hras+/+ (n = 17) and HrasG12S/+ (n = 18)). *p < 0.05, **p < 0.01 (Welch's t-test) compared with Hras+/+ mice. (c and d) Food intake and body weight gain in Hras+/+ and HrasG12S/+ mice fed a HFD from 5 to 16 weeks of age. The data are expressed as the mean ± SD (Hras+/+ (n = 7) and HrasG12S/+ (n = 7)). *p < 0.05 (Welch's t-test) compared with Hras+/+ mice. (e) Representative appearance of inguinal white adipose tissue (IWAT) and IWAT weight in Hras+/+ and HrasG12S/+ mice fed a HFD at 16 weeks and 1 year of age (Hras+/+ (n = 8) and HrasG12S/+ (n = 5)). *p < 0.05 (Mann-Whitney U-test) compared with Hras+/+ mice. (f) Survival rates of Hras+/+ and HrasG12S/+ mice fed a CD or a HFD (Hras+/+ CD (n = 13) and HrasG12S/+ CD (n = 18); Hras+/+ HFD (n = 17) and HrasG12S/+ HFD (n = 18)). *p < 0.05, **p < 0.01 (log-rank test) compared with Hras+/+ CD mice; ##p < 0.01 (log-rank test) compared with Hras+/+ HFD mice.

3.4. HrasG12S/+ Mice Fed a HFD Exhibit Impaired Fatty Acid Oxidation

Since HrasG12S/+ mice were resistant to HFD-induced obesity, we conducted a biochemical analysis of the blood and liver to examine the metabolic status of these mice. Serum LDL cholesterol levels were significantly higher in HrasG12S/+ mice fed a HFD than in Hras+/+ mice fed a HFD (Table 1). However, there were no differences in the other parameters. Gross observation of the livers revealed a yellowish, steatotic appearance in the 1-year-old Hras+/+ mice, whereas HrasG12S/+ mouse livers were normal (Fig. 3a). There were no significant differences in liver weight between the Hras+/+ and HrasG12S/+ mice that were fed either a HFD or a CD (Fig. 3b). The 1-year-old Hras+/+ mice fed a HFD exhibited hepatic steatosis with macrovesicular lipid droplets, whereas the corresponding HrasG12S/+ mice exhibited hepatic steatosis with microvesicular lipid droplets (Fig. 3c). Hepatic steatosis with microvesicular lipid droplets was already evident in HrasG12S/+ mice that had been fed a HFD for 11 weeks (Supplementary Fig. 4).

Table 1.

Biochemical parameters in Hras+/+ and HrasG12S/+ mice in fed or fasted state.

Fed
 Fasted
Hras+/+ HrasG12S/+ Hras+/+ HrasG12S/+
TP (g/dl) 5.0 ± 0.2 4.9 ± 0.2 5.0 ± 0.2 4.9 ± 0.2
Alb (g/dl) 3.6 ± 0.2 3.4 ± 0.2 3.6 ± 0.2 3.4 ± 0.2
BUN (mg/dl) 26.2 ± 5.7 21.4 ± 5.8 17.5 ± 5.4 18.2 ± 3.3
Creatinine (mg/dl) 0.1 ± 0.02 0.1 ± 0.02 0.2 ± 0.04 0.1 ± 0.02
UA (mg/dl) 2.9 ± 0.8 3.5 ± 0.4
Amy (IU/l) 2115.1 ± 391.3 1931.0 ± 119.8
AST (IU/l) 45.6 ± 6.3 51.0 ± 7.1 96.4 ± 21.0 77.8 ± 29.8
ALT (IU/l) 18.2 ± 2.8 19.6 ± 4.7 50.0 ± 26.7 35.8 ± 20.4
TG (mg/dl) 67.2 ± 59.8 34.2 ± 13.6 29.4 ± 13.4 41.8 ± 27.9
Total Cho (mg/dl) 98.6 ± 12.1 94.0 ± 15.2 99.0 ± 13.9 73.0 ± 10.7
F-Cho (mg/dl) 20.2 ± 2.8 20.8 ± 3.8 20.6 ± 2.6 13.4 ± 5.4#
E-Cho (mg/dl) 78.4 ± 10.4 73.2 ± 11.9 78.4 ± 12.2 59.6 ± 6.8
LDL-Cho (mg/dl) 6.8 ± 1.3 10.6 ± 1.8* 6.4 ± 2.3 6.0 ± 1.4##
HDL-Cho (mg/dl) 52.0 ± 7.1 46.6 ± 7.6 45.8 ± 4.8 37.8 ± 4.6
NEFA (μEq/l) 783.6 ± 343.9 647.2 ± 73.5 909.6 ± 197.3 1066.4 ± 170.3#
Total Bil (mg/dl) 0.1 ± 0.03 0.1 ± 0.07 0.1 ± 0.02 0.1 ± 0.02
TBA (μmol/l) 5.8 ± 6.3 14.8 ± 23.1 9.4 ± 5.5 9.4 ± 3.8
Insulin (ng/ml) 0.5 ± 0.2 0.4 ± 0.2
Leptin (ng/ml) 12.2 ± 6.6 6.0 ± 3.8
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The mice were fed a HFD from 5 to 16 weeks of age. Blood samples were obtained using the protocol (Supplementary Fig. 5). The data are expressed as the mean ± SD. (Hras+/+ (n = 5) and HrasG12S/+ (n = 5) in fed state. Hras+/+ (n = 5) and HrasG12S/+ (n = 5) in fasted state.) Significantly different than Hras+/+ in each fed and fasted conditons, *p < 0.05 (Tukey's test). Significantly different than fed condition in each Hras+/+ and HrasG12S/+ groupes, #p < 0.05, ##p < 0.01 (Tukey's test).

Fig. 3.

Fig. 3

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Hepatic microvesicular steatosis in HrasG12S/+ mice fed a HFD.

(a) Representative gross morphology of livers from Hras+/+ and HrasG12S/+ mice fed a HFD at 1 year of age. (b) Crude liver weight (left bar graph) and liver weight (LW) to body weight (BW) ratio (right bar graph) of Hras+/+ and HrasG12S/+ mice fed a CD or HFD at 1 year of age. The data are expressed as the mean ± SD (Hras+/+ (n = 11) and HrasG12S/+ (n = 8) for CD-fed mice; Hras+/+ (n = 8) and HrasG12S/+ (n = 8) for HFD-fed mice). (c) HE-stained liver sections from Hras+/+ and HrasG12S/+ mice fed a HFD at 1 year of age. The arrows and arrowheads indicate macrovesicular and microvesicular lipid drops, respectively. Scale bars = 100 μm (upper panel) and 50 μm (lower panel). (d) HE-stained liver sections from Hras+/+ and HrasG12S/+ mice fed a HFD under fed or fasted conditions at 16 weeks of age. Samples were obtained using the described protocol (Supplementary Fig. 5). Scale bar = 50 μm. (e–h) Samples were obtained according to the described protocol (Supplementary Fig. 5). Total lipid (e), triglyceride (f), total cholesterol (g) and free fatty acid (h) levels in the liver from fed or fasted Hras+/+ and HrasG12S/+ mice. The data are expressed as the mean ± SD (Hras+/+ (n = 5) and HrasG12S/+ (n = 6) in the fed condition; Hras+/+ (n = 6) and HrasG12S/+ (n = 6) in the fasted condition). **p < 0.01 (Welch's t-test) compared with fed Hras+/+ and HrasG12S/+ mice. (i-k) Blood glucose (i), urinary β-hydroxybutyric acid (j) and blood β-hydroxybutyric acid (k) levels in Hras+/+ and HrasG12S/+ mice. Blood and urinary samples were obtained as described (Supplementary Fig. 5). The data are expressed as the mean ± SD (Hras+/+ (n = 7) and HrasG12S/+ (n = 6) in the blood samples; Hras+/+ (n = 7) and HrasG12S/+ (n = 7) in the urinary samples). *p < 0.05, **p < 0.01 (Welch's t-test) compared with Hras+/+ mice.

Hepatic steatosis with microvesicular lipid droplets, which indicates fatty acid accumulation, is observed in cases of mitochondrial injury and impaired mitochondrial fatty acid oxidation (such as in Reye syndrome) (Fromenty et al., 1997, Fromenty and Pessayre, 1997). Under starvation conditions, patients with impaired mitochondrial fatty acid oxidation are not able to utilize fatty acids in the liver, which leads to increased free fatty acid levels in the blood, lipid accumulation in the liver, and decreased ketone body production (Vishwanath, 2016). To elucidate if the hepatic steatosis with microvesicular lipid droplets observed in HrasG12S/+ mice is caused by impaired mitochondrial fatty acid oxidation, we examined liver tissues, blood glucose levels, blood and urinary β-hydroxybutyric acid levels and serum biochemical parameters in fasted mice that were fed a HFD from 5 to 16 weeks of age (Supplementary Fig. 5).

Under fasted conditions, liver sections from HrasG12S/+ mice showed the accumulation of large lipid droplets (Fig. 3d). In contrast, Hras+/+ mice exhibited an increase in microvesicular lipid droplets in the liver. Serum non-esterified fatty acid (NEFA) levels, one free fatty acid (FFA) parameter, were significantly elevated in fasted HrasG12S/+ mice compared with non-fasted mice. In contrast, serum NEFA levels in Hras+/+ mice were comparable in fed and fasted conditions (Table 1). The hepatic levels of total cholesterol, triglycerides and free fatty acids were lower in HrasG12S/+ mice than in Hras+/+ mice on a HFD. However, under fasted conditions, the lipid content (including triglycerides, total cholesterol and free fatty acids) in the liver of HrasG12S/+ mice increased to the same levels as those in Hras+/+ mice. These liver histology and lipid content results (Fig. 3e-3h) suggested decreased FFA utilization in the liver of HrasG12S/+ mice in the fasted condition.

The blood glucose levels were comparable in HrasG12S/+ mice and Hras+/+ mice during 48 h of fasting (Fig. 3i). Urinary β-hydroxybutyric acid levels after 24 h of fasting were significantly lower in HrasG12S/+ mice than in Hras+/+ mice (Fig. 3j). Thereafter, blood β-hydroxybutyric acid levels were significantly reduced in HrasG12S/+ mice after 48 h of fasting (Fig. 3k), suggesting decreased ketone body production. A line of evidence suggests that under fasted conditions, HrasG12S/+ mice fed a HFD develop impaired fatty acid oxidation, including decreased lipid utilization in the liver, elevated levels of NEFA and hypoketosis.

3.5. HrasG12S/+ Mice Fed a HFD Exhibit an Increase in Long-Chain Fatty Acylcarnitines

Impaired mitochondrial fatty acid oxidation leads to hypercatabolism and an increase in various types of fatty acylcarnitines in the blood under starvation conditions (Vishwanath, 2016). After 24 h of fasting, tandem mass spectrometry analysis of blood acylcarnitine profiles showed a significant increase in long-chain fatty acylcarnitines, including C16, C18, C18:1 and C18:2, in HrasG12S/+ mice fed a HFD (Fig. 4a), suggesting decreased activity of an earlier step in mitochondrial fatty acid oxidation. In the blood amino acid profiles, the methionine and phenylalanine levels were significantly higher in HrasG12S/+ mice than in Hras+/+ mice (Fig. 4b), suggesting hypercatabolism.

Fig. 4.

Fig. 4

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Changes in parameters related to mitochondrial fatty acid oxidation in liver tissues from fed or fasted Hras+/+ and HrasG12S/+ mice.

(a and b) Relative blood acylcarnitine (a) and amino acid (b) levels in Hras+/+ and HrasG12S/+ mice after 24 h of fasting. Blood samples were obtained as described (Supplementary Fig. 5). The data are expressed as the mean ± SD (Hras+/+ (n = 7) and HrasG12S/+ (n = 7)). *p < 0.05, **p < 0.01 (Welch's t-test) compared with Hras+/+ mice. Val, valine; Leu, leucine; Ileu, Isoleucine; Met, methionine; Cit, citrulline; Phe, phenylalanine; Tyr, tyrosine; Arg, arginine; Ala, alanine. (c) Relative mRNA expression of genes related to mitochondrial β-oxidation in liver tissues from Hras+/+ and HrasG12S/+ mice (Hras+/+ (n = 6) and HrasG12S/+ (n = 7) in the fed condition; Hras+/+ (n = 6) and HrasG12S/+ (n = 6) in the fasted condition). Samples were obtained as described (Supplementary Fig. 5). mRNA levels of target genes were normalized to those of Gapdh. *p < 0.05,** p < 0.01 (Welch's t-test or Mann-Whitney U-test) compared with Hras+/+ mice.

In addition, we evaluated the mRNA expression of genes related to mitochondrial fatty acid oxidation. In the fed condition, the hepatic mRNA expression of peroxisome proliferator-activated receptor alpha (Pparα), acyl-CoA synthetase long-chain family member 1 (Acsl1), carnitine palmitoyltransferase 2 (Cpt2), medium-chain acyl-CoA dehydrogenase (Acadm) and mitochondrial trifunctional enzyme subunit beta (Hadhb) was significantly lower in HrasG12S/+ mice than in Hras+/+ mice (Fig. 4c). A significant decrease in Acadm and short-chain-3-hydroxyacyl-CoA dehydrogenase (Hadh) gene expression was observed in fasted HrasG12S/+ mice compared with Hras+/+ mice (Fig. 4c). These findings indicate that mitochondrial fatty acid oxidation is impaired in the livers of HrasG12S/+ mice.

3.6. HrasG12S/+ Mice Fed a HFD Exhibit Alterations in Glucose, Organic Acid and Glutamine Metabolism

We hypothesized that the introduction of the Hras G12S mutation in vivo causes metabolic changes in addition to those to fatty acid oxidation that might be similar to those observed in cancer cells (Bryant et al., 2014, Zheng et al., 2015, Zhou et al., 2016). We then performed comprehensive RT-qPCR analysis of genes involved in glucose, organic acid and glutamine metabolism in liver tissues (Supplementary Table 4). The mRNA levels of genes involved in glucose metabolism (glucose-6-phosphate dehydrogenase, G6pd) and glutaminolysis (aspartate aminotransferase 1, Got1) were significantly increased in fed and/or fasted HrasG12S/+ mice (Fig. 5a and b). Furthermore, pyruvate dehydrogenase alpha (Pdha) mRNA expression was significantly decreased in fed HrasG12S/+ mice, and glutaryl-CoA dehydrogenase (Gcdh), glutamate dehydrogenase 1 (Glud1) and malic enzyme 1 (Me1) mRNA levels were decreased in both fed and fasted HrasG12S/+ mice (Fig. 5a-5c). To evaluate the differences in glucose metabolism between Hras+/+ and HrasG12S/+ mice, we performed an intraperitoneal glucose tolerance test (IPGTT) and measured urinary pyruvic acid. HrasG12S/+ mice displayed significantly lower blood glucose levels than Hras+/+ mice after 30 min in the IPGTT (Fig. 5d). Moreover, HrasG12S/+ mice fed a CD showed significantly lower blood glucose levels after 30 min of fasting. HrasG12S/+ mice fed a HFD also had significantly lower blood glucose levels after 90 min of fasting (Supplementary Fig. 6a). Under these conditions, blood insulin levels after 90 min of fasting were comparable between Hras+/+ and HrasG12S/+ mice (Supplementary Fig. 6b). Urinary pyruvic acid levels after 24 h of fasting were significantly higher in HrasG12S/+ mice than in Hras+/+ mice (Fig. 5e). These results suggest that HrasG12S/+ mice fed a HFD show changes in glucose, organic acid and glutamine metabolism and indicate that fasting leads to insulin-independent early hypoglycemia and enhanced glutaminolysis.

Fig. 5.

Fig. 5

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Changes in hepatic gene expression related to glucose, organic acid and glutamine metabolism and glucose and pyruvic acid utilization in fed or fasted Hras+/+ and HrasG12S/+ mice.

(a–c) Samples were obtained as described (Supplementary Fig. 5). Relative mRNA expression levels of genes related to glucose (a), glutamine (b) and organic acid (c) metabolism in liver tissues from fed or fasted Hras+/+ and HrasG12S/+ mice. (Hras+/+ (n = 6) and HrasG12S/+ (n = 7) in the fed condition; Hras+/+ (n = 6) and HrasG12S/+ (n = 6) in the fasted condition). mRNA levels of target genes were normalized to those of Gapdh. The open circle (○) indicates an outlier. *p < 0.05, **p < 0.01 (Welch's t-test or Mann-Whitney U-test) compared with Hras+/+ mice. (d) IPGTT analysis of blood glucose levels in Hras+/+ and HrasG12S/+ mice at 16 weeks of age. The data are expressed as the mean ± SD (Hras+/+ (n = 8) and HrasG12S/+ (n = 5)). *p < 0.05, **p < 0.01 (Welch's t-test) compared with Hras+/+ mice. (e) Urinary pyruvic acid levels in Hras+/+ and HrasG12S/+ mice (Hras+/+ (n = 7) and HrasG12S/+ (n = 7)). Urine samples were obtained as described (Supplementary Fig. 5). The bars indicate the mean. Statistical analysis was performed using the Mann-Whitney U-test. (f) Western blotting of liver tissues from fasted Hras+/+ and HrasG12S/+ mice. The lower bar graphs show the relative phospho-ERK and phospho-AKT levels. The band intensity was normalized to that of the non-phosphorylated protein. The data are expressed as the mean ± SD (Hras+/+ (n = 5) and HrasG12S/+ (n = 5)). **p < 0.01 (Welch's t-test) compared with Hras+/+ mice.

We also performed western blotting to elucidate the signaling pathways altered in the HrasG12S/+ mouse liver. Phosphorylated ERK levels in the livers of Hras+/+ and HrasG12S/+ mice showed no significant differences under the fed condition (Supplementary Fig. 7). In contrast, the hepatic levels of phosphorylated ERK were significantly higher in fasted HrasG12S/+ mice than in fasted Hras+/+ mice (Fig. 5f). There were no significant differences between the Hras+/+ and HrasG12S/+ mice in the levels of phosphorylated AKT (Ser 473), which is activated by RAS signaling, or of phosphorylated AMPK (Thr 172), which is associated with fatty acid and glycogen metabolism and cell growth (Carling, 2004, Hardie, 2004) (Fig. 5f).

4. Discussion

In this study, we generated heterozygous Hras G12S knock-in mice as a mouse model of Costello syndrome to explore the implications of germline HRAS activation in vivo on metabolic homeostasis. HrasG12S/+ mice fed a HFD exhibited poor weight gain, decreased fatty acid oxidation and altered metabolism of glucose, organic acids and glutamine in the liver. Impaired fatty acid oxidation, hypoketosis and insulin-independent early hypoglycemia were clearly evident under fasted conditions after HFD feeding. Taken together, our results demonstrate that knock-in mice expressing germline Hras G12S exhibit impaired hepatic energy homeostasis when fed a HFD.

Our investigation revealed that HrasG12S/+ mice fed a HFD exhibit microvesicular steatosis with decreased mRNA levels of genes involved in fatty acid oxidation, suggesting impaired mitochondrial function and mitochondrial fatty acid oxidation. Furthermore, increased lipid accumulation in the liver, blood methionine and phenylalanine levels, and long-chain fatty acylcarnitines, including C16, C18, C18:1 and C18:2, and decreased ketone body and blood glucose levels were observed in fasted HrasG12S/+ mice. Abnormal accumulation of long-chain fatty acylcarnitines, including C12–18, is observed in patients with mitochondrial trifunctional protein (MTP), CPT2 and carnitine-acylcarnitine translocase (CACT) deficiencies (Hori et al., 2010, Olpin et al., 2005, Rubio-Gozalbo et al., 2004). Biallelic Mtp knockout mice have been shown to exhibit microvesicular hepatic steatosis, neonatal hypoglycemia, sudden death and elevations of C14, C16, C16:1, C18:1 and C18:2 acylcarnitines, whereas heterozygous Mtp knockout mice do not show hypoglycemia (Ibdah et al., 2001). A recent publication on liver-specific Cpt2 knockout mice reported microvesicular hepatic steatosis and significantly low levels of serum β-hydroxybutyric acid without hypoglycemia (Lee et al., 2016). Moreover, recent studies have reported mitochondrial dysfunction in both HRAS-transformed cells and patients with RASopathies (Aeby et al., 2007, Biaglow et al., 1997, Kleefstra et al., 2011, Telang et al., 2007, Yang et al., 2010). It is possible that impaired mitochondrial fatty acid oxidation is associated with hypoglycemia, poor weight gain and cardiomyopathy in patients with Costello syndrome.

HrasG12S/+ and HrasG12V knock-in mice exhibited no growth retardation or feeding difficulty on the control diet (Chen et al., 2009, Schuhmacher et al., 2008). However, HrasG12S/+ mice developed a lean phenotype with poor weight gain, reduced adiposity and fat malabsorption during HFD feeding. The mouse model of Noonan syndrome with multiple lentigines (LS mice) expressing a heterozygous Ptpn11 T468M mutation exhibited resistance to HFD-induced obesity and reduced adiposity (Tajan et al., 2014), which are similar findings to those of our present study. Furthermore, LS mice show decreased adipogenesis, increased energy expenditure and enhanced insulin signaling. MEK inhibitors lead to increased body weight and adiposity in LS mice and increased body weight in the mouse model of Noonan syndrome and CFC syndrome (Inoue et al., 2017, Tajan et al., 2014, Wu et al., 2011). Interestingly, mouse models of CFC syndrome from our group and another group also exhibited a reduction in adiposity (Urosevic et al., 2011). A recent study showed that patients with Costello syndrome exhibit an increased energy expenditure (Leoni et al., 2016). Patients with Noonan or CFC syndrome have been shown to have intestinal lymphangiectasia, which results in fat malabsorption and growth retardation (Joyce et al., 2016, Mistilis et al., 1965, Vignes and Bellanger, 2008). Thus, these metabolic alterations, including decreased adipogenesis, fat malabsorption, lymphatic disorders, increased energy expenditure and enhanced insulin signaling, may be common in RASopathies. Future studies will increase our understanding of the mechanism behind the lean phenotype of HrasG12S/+ mice fed a HFD.

Normal differentiated cells metabolize glucose to carbon dioxide through the mitochondrial tricarboxylic acid (TCA) cycle, which is the most effective way to generate ATP. In contrast, cancer cells prefer to metabolize glucose to lactate through glycolysis under aerobic conditions, which is known as “the Warburg effect” (Warburg, 1956). Several reports have suggested that the RAS oncogene promotes anaerobic glycolysis, glucose uptake, lipid synthesis and nucleotide synthesis through the pentose phosphate pathway (PPP) (Tian et al., 1998). Under both fed and fasted conditions, the metabolic alterations observed in HrasG12S/+ mice (Fig. 6), including changes in glucose, organic acid and glutamine metabolism, are similar to those in several previous reports on cancer. For example, HRAS-transformed human breast epithelial cells have been reported to have increased glycolysis and lactate production and enhanced expression of G6pd, which encodes a PPP regulatory enzyme (Zheng et al., 2015). Moreover, approximately 50% of diethylnitrosamine-induced liver tumors have HRAS mutations in codon 61, an HRAS hot spot in cancer. In a microarray analysis, diethylnitrosamine-induced liver tumors showed upregulation of G6pd, which is involved in glycolysis, and downregulation of GCDH and ME1, which are involved in organic acid and glutamine metabolism (Unterberger et al., 2014). These results were similar to the phenotype of HrasG12S/+ mice fed a HFD (Fig. 6). Studies of pancreatic ductal adenocarcinoma with a KRAS mutation showed an upregulation of glycolysis-associated genes, including glucose transporter 1 (GLUT1), hexokinase 1 and 2 (HK1 and HK2), phosphofructokinase 1 (PFK1) and lactate dehydrogenase A (LDHA) (Bryant et al., 2014, Son et al., 2013). In addition, these cancers exhibited an upregulation of GOT1 and GOT2 and a downregulation of GLUD1. These results are somewhat similar to our results, in which hepatic phosphorylated ERK levels and Got1 expression increased in fasted HrasG12S/+ mice after HFD feeding (Fig. 5b and f). Collectively, somatic RAS mutations and the germline Hras G12S mutation in mice are associated with glucose, organic acid and glutamine metabolism.

Fig. 6.

Fig. 6

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Schematic of the metabolic changes in the liver of fed and fasted HrasG12S/+ mice.

(a and b) Changes in gene expression in the liver of HrasG12S/+ mice under fed (a) and fasted (b) conditions. Upregulated or activated proteins and genes are shown in red. Decreased gene expression is shown in blue. (a) In the fed condition, the pentose phosphate pathway is activated due to an increase in G6pd gene expression. A decrease in Pdha gene expression inhibits the conversion of pyruvate to acetyl-CoA. Low Glud1 and Got2 gene expression results in a decrease in alpha-ketoglutaric acid. In the fatty acid oxidation pathway, decreased Acsl1, Cpt2, Acadm and Hadhb gene expression leads to a lack of acetyl-CoA. (b) In the fasted condition, the Hras G12S mutation leads to increased Got1 expression and decreased Glud1 expression through ERK activation. The G6pd gene is also activated in the fed condition. Upregulation of Got1 and downregulation of Glud1 lead to diminished levels of alpha-ketoglutaric acid, which is used to produce ATP in the TCA cycle. The reduced gene expression of Acadm and Hadh leads to impaired fatty acid oxidation, which is the main energy supplier under conditions of starvation. Gln, glutamine; Glu, glutamate; Asp, aspartic acid; OAA, oxaloacetic acid; α-KG, alpha-ketoglutaric acid.

HrasG12V knock-in mice have been generated in two laboratories. Phenotypes between two HrasG12V knock-in mice were different because of the different genetic background. HrasG12V knock-in mice reported by Schumacher et al. showed normal weight and size, facial dysmorphia, cardiomegaly with cardiomyocyte hypertrophy, aortic valve thickening, cardiac and kidney fibrosis. However, tumor development was rare in these mice (Schuhmacher et al., 2008). In contrast, HrasG12V knock-in mice reported by Chen et al., showed high perinatal lethality, dysmorphic facial features, defective dental ameloblasts, malocclusion, papillomas and angiosarcomas, but did not develop any cardiac defects (Chen et al., 2009). In this study, HrasG12S/+ mice exhibited dysmorphic facial features (including a round head and a shortened nasal bridge), a malocclusion, cardiomegaly with cardiomyocyte hypertrophy and kidney fibrosis. These phenotypes were reminiscent of the characteristic features of Costello syndrome patients and HrasG12V knock-in mice (Chen et al., 2009, Schuhmacher et al., 2008, Viosca et al., 2009). However, the papillomas and angiosarcomas reported in HrasG12V knock-in mice (Chen et al., 2009) were not observed in HrasG12S/+ mice, even at 1 year of age. These differences are consistent with the higher cancer frequency associated with HRAS G12V than with HRAS G12S and the higher population of the GTP-bound active form of HRAS G12 V than HRAS G12S ((Wey et al., 2013) and the cosmic database). HrasG12S/+ mice also exhibited rectal prolapse, metabolic changes, a unilateral cystic kidney and glomerulopathy, which have not been reported in HrasG12V knock-in mice. Although histological examination of the kidneys of patients with Costello syndrome have not been reported, ultrasonographic changes, including pelviectasis, hydronephrosis, increased kidney size and echogenic kidneys, have been observed in RASopathy patients during the perinatal period (Myers et al., 2014), suggesting a presymptomatic state of polycystic kidneys (Avni et al., 2002). Indeed, polycystic kidneys have been observed in Hras G12V transgenic mice (Gilbert et al., 1997, Schaffner et al., 1993). These results suggest that oncogenic HRAS mutations may be associated with the development of renal cysts.

Here, we developed HrasG12S/+ mice as a model that recapitulates the pathophysiology of Costello syndrome. Our study provides evidence that individuals expressing the germline Hras G12S mutation could have altered energy homeostasis when consuming a HFD. Given that cells with oncogenic RAS mutations exhibit cancer-specific alterations in energy homeostasis, our HrasG12S/+ mice will provide an in vivo model for studying cancer metabolism. Additional studies will be necessary to understand the precise mechanism of energy homeostasis in HrasG12S/+ mice and in patients with Costello syndrome and cancer.

Acknowledgments

Acknowledgements

We wish to thank Riyo Takahashi, Kumi Kato and Yoko Tateda for technical assistance and Hiroaki Nagao and Kenji Yoshiwara for technical assistance and discussions of the experimental data. We would also like to acknowledge the support of the Biomedical Research Core of the Tohoku University Graduate School of Medicine.

Funding Sources

This work was supported by the Funding Program for the Next Generation of World-Leading Researchers (NEXT Program) from the Ministry of Education, Culture, Sports, Science and Technology of Japan to Y.A. (LS004), the Grants-in-Aid by the Practical Research Project for Rare/Intractable Diseases from the Japan Agency for Medical Research and Development, AMED to Y.A. (16eK0109021,17894363), by the Japan Society for the Promotion of Science (JSPS) KAKENHI Grant Number 26293241 and 16K15522 to Y.A., and by JSPS KAKENHI Grant Number 15K19598 to S.I.

Conflicts of Interest

There are no conflicts of interest.

Author Contributions

D.O., S.I., Y.M. and Y.A. designed the experiments and wrote the manuscript. D.O., S.I, S.M, S.T., M.M., Y.N., S.Y. and Y.A. conducted experiments. D.O., S.I, S.M., Y.N., T.N., S.Y. Y.M. and Y.A. contributed to data analysis.

Footnotes

Appendix A

Supplementary data to this article can be found online at https://doi.org/10.1016/j.ebiom.2017.11.029.

Contributor Information

Shin-ichi Inoue, Email: sinoue@med.tohoku.ac.jp.

Yoko Aoki, Email: aokiy@med.tohoku.ac.jp.

Appendix A. Supplementary data

Supplementary material

mmc1.docx (6.4MB, docx)

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