Skip to main content
PMC home page
PLOS ONE logoLink to PLOS ONE
. 2008 Jan 9;3(1):e1405. doi: 10.1371/journal.pone.0001405

Polymorphisms of the TUB Gene Are Associated with Body Composition and Eating Behavior in Middle-Aged Women

Jana V van Vliet-Ostaptchouk 1,2, N Charlotte Onland-Moret 3,4, Ronit Shiri-Sverdlov 2, Patrick J J van Gorp 2, Anne Custers 2, Petra H M Peeters 4, Cisca Wijmenga 3,5, Marten H Hofker 1,2, Yvonne T van der Schouw 4,*
Editor: Philippa Talmud6
PMCID: PMC2157487  PMID: 18183286

Abstract

Background

The TUB gene, encoding an evolutionary conserved protein, is highly expressed in the hypothalamus and might act as a transcription factor. Mutations in TUB cause late-onset obesity, insulin-resistance and neurosensory deficits in mice. An association of common variants in the TUB gene with body weight in humans has been reported.

Methods/Findings

The aim was to investigate the relationship of single nucleotide polymorphisms (SNPs) of the TUB gene (rs2272382, rs2272383 and rs1528133) with both anthropometry and self-reported macronutrient intake from a validated food frequency questionnaire. These associations were studied in a population-based, cross-sectional study of 1680 middle-aged Dutch women, using linear regression analysis. The minor allele C of the rs1528133 SNP was significantly associated with increased weight (+1.88 kg, P = 0.022) and BMI (+0.56 units, P = 0.05). Compared with non-carriers, both AG heterozygotes and AA homozygotes of the rs2272382 SNP derived less energy from fat (AG: −0.55±0.28%, P = 0.05, AA: −0.95±0.48%, P = 0.047). However, both genotypes were associated with an increased energy intake from carbohydrates (0.69±0.33%, P = 0.04 and 1.68±0.56%, P = 0.003, respectively), mainly because of a higher consumption of mono- and disaccharides. Both these SNPs, rs2272382 and rs1528133, were also associated with a higher glycemic load in the diet. The glycemic load was higher among those with AG and AA genotypes for the variant rs2272382 than among the wild types (+1.49 (95% CI: −0.27–3.24) and +3.89 (95% CI: 0.94–6.85) units, respectively). Carriers of the minor allele C of rs1528133 were associated with an increased glycemic load of 1.85 units compared with non-carriers.

Conclusions

Genetic variation of the TUB gene was associated with both body composition and macronutrient intake, suggesting that TUB might influence eating behavior.

Introduction

The hypothalamus plays a central role in the control of energy balance and the regulation of body weight and food intake [1]–[3]. The tubby protein is highly expressed in the paraventricular (PVN), ventromedial (VMH), and arcuate nuclei (ARC) of the hypothalamus that regulate satiety and appetite [4]–[6]. Loss-of-function mutations in tubby result in late-onset obesity, insulin resistance and neurosensory deficits in mice [7]. Further investigations showed that the expression of different neuropeptides was altered. Lower levels of agouti-related protein (AGRP) and proopiomelanocortin (POMC) mRNA levels in ARC were paralleled by increased levels of neuropeptide Y (NPY) in the dorsomedial-ventromedial hypothalamus (DMH/VMH) as well as preproorexin mRNA in the lateral hypothalamus (LHA) in mature and juvenile tubby mice [8]–[10]. Such multiple derangements in the neural system lead to hyperphagia in the adult animals [8].

Tubby homologs are highly conserved among vertebrate genomes [11] and in C. elegans the important role of the tubby ortholog, tub-1, in fat storage regulation has been shown [12]–[14]. Several studies have suggested that tubby may function as a transcription factor and/or as an adaptor molecule for downstream signaling of insulin and/or G-protein-coupled receptors [15]–[17].

Previously, we reported a significant association between variants in the TUB gene and body mass index (BMI) in a Dutch population of type 2 diabetes patients [18]. The minor alleles of single nucleotide polymorphisms (SNPs) rs2272382, rs2272383 and rs1528133 were associated with an average of 1.5 kg/m2 higher BMI, and were 1.3 times more frequent among obese people (BMI> = 30 kg/m2) than lean individuals (BMI<25 kg/m2).

In order to ascertain the validity of our previous results in a population-based sample, and to explore whether macronutrient intake may be involved in the development of overweight and/or obesity, the present study investigated the effects of genetic variants in the TUB gene on food intake and body composition in middle-age Dutch women.

Materials and Methods

Subjects

The women included in this study are Dutch participants in the European Prospective Investigation into Cancer and Nutrition (EPIC), conducted in Utrecht, the Netherlands (Prospect-EPIC) [19]. Between 1993 and 1997, 17,357 women aged 49–70 years and residing in or near Utrecht were recruited through a regional, population-based, breast cancer screening program. All the women signed written informed consent and the study was approved by the Institutional Review Board of the University Medical Center Utrecht.

At recruitment, each participant filled out a general questionnaire on lifestyle factors, gynecological and obstetric history, and past and current morbidity, as well as a validated semi-quantitative food frequency questionnaire (FFQ) with the aim of capturing the habitual diet during the year preceding enrolment. In addition, pulse rate, blood pressure and anthropometric measurements were taken and a blood sample was donated and stored at −196°C. A random sample of 1736 (10%) women was taken for biochemical analyses. Buffy coat samples were missing for 56 women, so the study population comprised 1680 women.

Anthropometry variables

Body height was measured to the nearest 0.5 cm with a wall mounted stadiometer (Lameris, Utrecht, the Netherlands). Body weight was measured in light indoor clothing without shoes to the nearest 0.5 kg with a floor scale (Seca, Atlanta, GA, USA). Body mass index (BMI) was calculated as weight divided by height squared (kg/m2). Waist and hip circumferences were measured to the nearest 0.5 cm with a standard household tape measure, and the waist-to-hip ratio was calculated.

Food frequency questionnaire

The FFQ contains questions on the usual frequency of consumption of 77 main food items during the year preceding enrollment. Further information was sought on consumption frequency for different sub-items, preparation methods, and additions. Color photographs were used to estimate portion size for 28 food items. Overall, the questionnaire allows the estimation of the average daily consumption of 178 foods, by asking about sub-items for several foods, like fruit and vegetables, in additional questions. The FFQ was validated in pilot studies prior to the start of our study [20]. We calculated glycemic load by multiplying the glycemic index of a food with its carbohydrate content, then multiplied this value with the frequency of consumption of this food, and summed the values over all food items [21]. Glycemic load thus represents both the quality and quantity of carbohydrates and the interaction between the two. Each unit of dietary glycemic load represents the equivalent of 1 g carbohydrate from glucose. The overall glycemic index of a woman's diet was calculated by dividing the dietary glycemic load by the total amount of carbohydrate consumed [21]. Such expression of dietary glycemic index per gram of carbohydrate thus reflects the overall quality of the daily carbohydrate intake.

Genotyping

DNA was extracted from whole blood using the QIAamp® Blood Kit (Qiagen Inc., Valencia, CA, USA). SNPs rs2272382, rs2272383 and rs1528133, previously reported to be associated with BMI (18), were genotyped using Taqman assay-on-demand (Applied Biosystems, Foster City, CA, USA). Assays were performed according to the manufacturer's specifications (assays C_86243_10, C_271936_1, C_9597097_1, respectively). The genotypes were analyzed using a TaqMan 7900HT (Applied Biosystems, Foster City, CA, USA). The DNA samples were processed in 384-well plates, each containing 4 negative controls and 12 genotyping controls (four duplicates of three different samples obtained from the Centre d'Etude du Polymorphisme Humain or CEPH). The genotype success rates were always >95% (95.7% for rs2272382, 96.5% for rs2272383 and 96.4% for rs1528133). The SNPs did not significantly deviate from Hardy-Weinberg equilibrium (χ2 = 0.41, p = 0.52 for rs2272382, χ2 = 1.38, p = 0.24 for rs2272383 and χ2 = 0.24, p = 0.63 for rs1528133). There were no discordances in the genotypes of any of the CEPH samples.

Statistical analysis

All statistical analyses were performed using the SPSS program, version 13.0 for Windows (SPSS, Chicago, IL, USA). Means with standard deviation, median and range (for the not-normally distributed characteristics) or frequencies (where appropriate) of baseline characteristics were presented for the entire population. The genotype frequencies were tested for Hardy-Weinberg equilibrium using a χ2 test with 1 df. The association between genotypes of SNPs and the cohort's anthropometrical characteristics and macronutrient intakes were calculated using a linear regression model. Individuals homozygous for the common allele served as the reference group. Linkage disequilibrium (LD) among SNPs was computed using Haploview program, version 4.0RC1 [22].

Results

We genotyped the three SNPs (rs2272382, rs2272383 and rs1528133) reported to be significantly associated with BMI in our previous study [18]. Figure 1 shows the structure of the TUB gene and its 3′ flanking region and the position of the genotyped SNPs. The allele frequencies of the variants as well as the pairwise linkage disequilibrium among SNPs were comparable with those reported by Shiri-Sverdlov et al (18) (Figure 1B,C). The haplotype analysis of the three genotyped SNPs revealed five common haplotypes (Figure 1,D).

Figure 1. Gene structure, location and characteristics of the genotyped SNPs, linkage disequilibrium (LD) among SNPs and the haplotype structure.

Figure 1

Open in a new tab

A: The upper panel shows the 90-kb region of chromosome 11p15.5 containing the TUB gene and the 3′ flanking RIC3 gene. Coding sequences (black), UTRs (white) and introns are indicated. B: Location (according to the NCBI 35 release), the alleles and the minor allele frequencies (MAF) of the SNPs. C: The pairwise LD plot, calculated as r2, among SNPs, with red colour indicating increasing level of LD as measured by D'. D: The three genotyped SNPs resulted in five common haplotypes.

Food intake and anthropometrical characteristics of the 1680 women are shown in Table 1 . First, we investigated the association of genetic variants of the TUB gene with different measures of body composition. The variant rs1528133 was significantly associated with weight and BMI ( Table 2 ). The carriers of the minor allele C had an average increase in weight of 1.88 kg (95% CI: 0.27–3.48) and of 0.56 units in BMI (95% CI: 0.0–1.12) compared with non-carriers. The same trend was observed for waist and hip circumferences, but it was less pronounced.

Table 1. Anthropometrical and food intake characteristics of 1680 women from the EPIC Cohort1.

graphic file with name pone.0001405.t001.jpg

Open in a new tab
1

All values are mean±SD

Table 2. Anthropometrical characteristics of 1680 women from the EPIC study by genotype for rs1528133 SNP in the TUB gene.

rs1528133
AA (n = 1392) AC+CC (n = 217+10)
Mean±SD β 95% CI p-value
Weight (kg) 69.56±0.30 1.88 0.27–3.48 0.022
Waist (cm) 83.13±0.26 1.23 −0.17–2.64 0.09
Hip (cm) 105.13±0.22 1.10 −0.07–2.27 0.06
BMI (kg/m2) 25.81±0.11 0.56 0.0–1.12 0.050
Waist-to-hip ratio 0.79±0.0 0.0 0.0–0.01 0.40
Open in a new tab

Table 3 shows intake of macronutrients, expressed as a percentage of total energy intake, according to the TUB gene SNPs. The rs2272382 variant was significantly associated with fat and carbohydrate intake. In comparison with non-carriers, the percentage of energy derived from fat was 0.55% (95% CI: −1.10–0.00) less in heterozygotes and 0.95% (95% CI: −1.88–−0.01) less in homozygotes for the minor allele A. The observed differences were mainly due to a lower percentage of energy derived from saturated and monounsaturated fats. However, both AG- and AA-genotypes showed significant association with higher carbohydrate intake compared with GG-genotype (0.69% (95% CI: 0.03–1.34) and 1.68% (95% CI: 0.58–2.78), respectively), mainly because of a higher consumption of mono- and disaccharides. A similar but weaker pattern of association with a lower percentage of energy from fat and higher percentage of energy from carbohydrates was found for the minor allele of rs2272383. No differences were observed in total energy intake and the intake of other macronutrients (data not shown). Adjustment for age and BMI did not alter the results (data not shown).

Table 3. Association of dietary phenotypes with the single nucleotide polymorphisms in the TUB gene.

rs2272382
GG ( n = 736) AG (n = 712) AA (n = 160)
Macronutrient intake (% of energy) Mean intake±SD β 95% CI p-value β 95% CI p-value
Protein intake 16.28±0.09 −0.27 −0.52–−0.03 0.028 0.04 −0.37–0.46 0.84
Fat intake 35.77±0.19 −0.55 −1.10–0.00 0.05 −0.95 −1.88–−0.01 0.047
Saturated fat 15.44±0.10 −0.32 −0.61–−0.04 0.027 −0.38 −0.86–0.10 0.12
Monounsaturated fat 13.30±0.09 −0.20 −0.45–0.05 0.11 −0.54 −0.95–−0.12 0.011
Polyunsaturated fat 6.72±0.06 −0.03 −0.21–0.16 0.78 −0.02 −0.33–0.28 0.88
Carbohydrates intake 44.32±0.23 0.69 0.03–1.34 0.040 1.68 0.58–2.78 0.003
Mono- and disaccharides 23.68±0.21 0.86 0.26–1.47 0.005 1.08 0.06–2.10 0.038
Polysaccharides 20.59±0.14 −0.17 −0.58–0.24 0.42 0.60 −0.09–1.29 0.09
Alcohol intake 3.62±0.17 0.14 −0.34–0.62 0.58 −0.77 −1.58–0.04 0.06
Open in a new tab

The analysis of association between SNPs of the TUB gene and glycemic load (GL) and glycemic index (GI) is shown in Table 4 . Two SNPs, rs2272382 and rs1528133, were associated with a higher GL in the diet. The GL was higher among those with AG and AA genotypes for the variant rs2272382 than among the wild types (+1.49 (95% CI: −0.27–3.24) and +3.89 (95% CI: 0.94–6.85) units, respectively). Carriers of the minor allele C of rs1528133 were also associated with an increased GL of 1.85 units compared with non-carriers. We observed no association of the TUB gene SNPs with glycemic index.

Table 4. Association of glycemic load (GL) and glycemic index (GI) with the single nucleotide polymorphisms in the TUB gene.

Glycemic load
SNP Wild type Heterozygote Minor homozygote
Mean intake±SD β 95% CI p-value β 95% CI p-value
rs2272382 99.26±0.61 1.49 −0.27–3.24 0.097 3.89 0.94–6.85 0.010
rs2272383 99.62±0.68 0.97 −0.83–2.77 0.29 1.37 −1.26–4.00 0.31
rs1528133 (hetero- and minor homo-zygotes combined) 99.33±0.64 1.85 0.13–3.57 0.035 - - -
Open in a new tab

Discussion

This study shows association between polymorphisms in the TUB gene and body composition, fat and carbohydrate intake, and glycemic load in a Dutch female population.

In a previous study, we found that common variants of the TUB gene can influence body weight and contribute to obesity in diabetics [18]. In this study, we have confirmed that the minor allele for rs1528133 is significantly associated with increased weight and BMI, and thus show that the relation of TUB with body composition can be extended to a general population.

In addition, we found a significant association between rs1528133 and specifically the intake of food with a higher glycemic load. Variant rs2272382 was also related to the differences in macronutrients intake and glycemic load: individuals carrying the minor allele A of rs2272382 derived significantly less of their energy from fat, especially saturated and monounsaturated fat, and more from carbohydrates, in particular mono- and disaccharides, than carriers of the major G allele. Moreover, subjects carrying both the AA and AG genotype showed an association with higher glycemic load. These observed differences in macronutrient intakes were not related with the total energy intake.

Both SNPs rs1528133 and rs2272382 are located in noncoding regions and thus are not likely to be functional variants. The rs1528133 polymorphism is located in the intron of the RIC3 gene, which is flanking the 3′ end of TUB. RIC3 is playing a role in neurotransmission [23] and can not, therefore, be excluded as a candidate gene for obesity. However, the observed association is more likely to be due to the strong linkage disequilibrium of rs1528133 with SNPs in the highly conserved 3′ end of the TUB gene (Figure S1), since the mutations in this part of TUB are known to cause obesity in tubby mice [6], [24]. In addition, we explored the pairwise LD between the rs2272382, rs2272383 and rs1528133 variants of TUB and other SNPs in the gene using HapMap CEU data. The analysis did not reveal any linkage of these SNPs with the known coding polymorphisms. Hence, it remains unclear whether the associated SNPs are in the LD with a yet unknown causal variant or are themselves functional by affecting the gene expression. To date, the difference in the tubby protein expression between obese and normal weight individuals was lately reported [25]. Altogether, all of this implies the importance of further investigation into the TUB role in human obesity.

The strengths of the current study include its large sample size and its population-based design, combined with the extensive dietary information collected through a validated instrument. In spite of observations that overweight individuals tend to underestimate their food intake [26]–[28], we did find associations with fat and carbohydrate intake, and glycemic load. Nevertheless, we cannot exclude the possibility that small effects on total energy intake may have been diluted to null because of this underestimation.

It needs to be noted that the current study was restricted to women. However, in the previous study we observed a statistically significant association between the TUB gene variants and BMI in both women and men (Shiri-Sverdlov, unpublished data).

The findings of the present study reveal that the carriers of the TUB variants who have an increased BMI and body weight consumed a diet high in carbohydrates, in particular because of their intake of mono- and disaccharides. Also, the positive association between these variants and glycemic load compared with non-carriers suggests that the effect of the TUB gene on body composition might be due to the increased intake of simple carbohydrates.

Recently, some evidence has accumulated that daily caloric intake and the selection of macronutrients in the diet are partly inherited [29]–[31]. It has been suggested that neuropeptides known to regulate eating behavior might influence the intake of specific nutrients [32] and effects of polymorphisms in these genes on macronutrient intake in humans has been reported [33]–[36]. Recent studies have shown that a polymorphism of the serotonin 5-HT receptor (5HT2A) gene is a risk factor for anorexia nervosa [37] and that it also has an effect on food intake. The risk allele A was associated with decreased fat intake in young people [34] and the G allele was related to increased carbohydrate and alcohol intake in obese individuals [35]. Loos et al have described the effect of genetic variants in the AGRP gene, associated with leanness, on fat and carbohydrate intakes [36].

The TUB is highly expressed in the paraventricular (PVN), ventromedial (VMH), and arcuate nuclei (ARC) of the hypothalamus that regulate satiety and appetite [4]–[6], [38], [39]. The exact mechanism linking the loss of the TUB function in the tubby mice, and their adult-onset obesity is still not clear. However, alteration of the expression of different neuropeptides in mutant animals has been observed, such as upregulation of neuropeptide Y (NPY) by ∼30-fold in the dorsomedial-ventromedial hypothalamus (DMH/VMH) of mature tubby mice [9], as well as altered expression of the agouti-related protein (AGRP) in the ARC nuclei of the hypothalamus [8]. Recently, it was shown that preproorexin mRNA in the lateral hypothalamus (LHA) of the juvenile non-obese tubby mice was upregulated by ∼60-fold, which resulted in increased orexin A protein levels [10]. Such disturbance in the expression of different neuropeptides, caused by loss-of-function mutations in TUB, suggests it plays an important role in the system controlling the appetite and feeding behavior. Hence, we hypothesized that TUB plays a role in modulating food intake.

The results of the present study show, for the first time, that genetic variation of the TUB gene might influence food preferences in humans. To our knowledge, no explicit studies of the “tub effect” on feeding behavior in animals have been performed either, except for the reported hyperphagia in the adult tubby mice compared to their normal littermates [8]. Thus, it is unknown how TUB can stimulate the selective intake of macronutrients. Nevertheless, there are several possible mechanisms that might explain our observations ( Figure 2 ). First, TUB may exert its effect through NPY, which is known to be positively linked to an animal's voluntary selection of carbohydrates and it has been suggested it plays a role in the signaling of deficiency of glucose availability, -stores or -utilization [40]. Second, TUB may influence the intake of fat through AGRP, shown to increase the preferences towards a high-fat diet in animals [41], [42]. Third, the possible interconnections between TUB and orexin, which is highly responsive to changes in circulating and dietary nutrients [40], are indicated by its high upregulation in the young tubby mice. Moreover, orexin was reported to interact with serotonin (5-HT) in appetite regulation [43]. Interestingly, tub has also been shown to translocate from the plasma membrane to the nucleus after serotonin activation of 5-HT2c receptors [15], which could point to a function of tub as a downstream effector of these receptors.

Figure 2. The interactions between the neuropeptides in the hypothalamus regulating energy homeostasis and its alteration in tubby mice.

Figure 2

Open in a new tab

Signals related to diet and circulating nutrients (shown at the bottom), which stimulate (+) or inhibit (−) the production of peptides, are received by the various hormonal receptors in the ARC nuclei, which contain NPY/AGRP- and POMC/CART-producing groups of cells. The activation of NPY/AGRP neurons promotes food intake, whereas POMC/CART neurons have the opposite effect. Both signals project onto LHA neurons that express MCH and orexin (important stimulators of food intake), which are also mediated by dopamine, serotonin and endocannabinoids. The loss of the TUB function in tubby mice causes alteration in the expression of different neuropeptides, such as AGRP, NPY and POMC in ARC, as well as upregulation of NPY by ∼30-fold in DMH/VMH and orexin by ∼60-fold in LHA (highlighted in red). The image of tubby mice was provided by J.Naggert and P. Nishina (Nat. Genet. 39,149; 2007). Abbreviations: AGRP, agouti-related protein; ARC, arcuate nucleus; CART, cocaine–amphetamine-regulated transcript; DMH and VMH, dorsomedial and ventromedial hypothalamus; LHA, lateral hypothalamus; MCH, melanin-concentrating hormone; NPY neuropeptide Y; POMC, pro-opiomelanocortin.

An important question remains how a high-carbohydrate diet can influence body weight. Observational studies have suggested that the type of carbohydrates consumed may be related to body weight [44]–[46], and this was supported by the results of a recent trial in which both high-protein and low- glycemic index (GI) regimens led to a greater loss of body fat, but cardiovascular risk reduction was optimized by a high-carbohydrate, low-GI diet [47].

The importance of glycemic load (GL) compared with glycemic index (GI) was emphasized before [48]. GI indicates carbohydrate quality, and ranks how rapidly a particular food turns into sugar, whereas GL reflects both the quality and quantity of carbohydrate in the diet. Therefore, GL may better characterize a food's physiological effect than the amount of carbohydrates or its GI [49]. Based on the results of our study, it can be speculated that TUB may represent a genetic component influencing eating preferences towards the high-GL diet, which results in the increased weight and BMI. Additional investigations should be carried out in other populations to understand the exact mechanism of TUB on food intake.

In conclusion, this study has shown for the first time that polymorphisms of the TUB gene, previously shown to influence body weight, are also associated with differences in macronutrients intake and glycemic load and could thus be related to eating behavior in humans. However, replication studies in other populations are necessary to confirm our findings. Further functional studies of TUB could also clarify the observed effects on food intake and reveal the physiological role of that gene in the central regulation of body weight and food intake.

Supporting Information

Figure S1

Detailed picture of TUB gene and it's 3′ flanking region and the location of all SNPs currently to be found in HapMap in this region (http://www.hapmap.org). The pairwise linkage disequilibrium (LD) plot, calculated as r2, among SNPs is shown, with red colour indicating increasing level of LD as measured by D'. The red boxes indicate SNPs genotyped in this study.

(11.07 MB EPS)

Click here for additional data file. (10.6MB, eps)

Acknowledgments

We would like to thank Jackie Senior for editing the manuscript, and Laurens Voogd and Frans Banky for helping with DNA aliquots.

Footnotes

Competing Interests: The authors have declared that no competing interests exist.

Funding: We thank the Dutch Diabetes Foundation, the European Vascular Genomics Network, and SenterNovem (IOP Genomics IGE05012) for financial support. The Prospect-EPIC study was financed by the European Commission-Europe Against Cancer (WHO AEP/90/05), the Dutch Ministry of Health, the Dutch Prevention Fund, the LK Research Fund, and the World Cancer Research Fund (WCRF 98A04 and WCRF 2000/30).

References

  • 1.Morton GJ, Cummings DE, Baskin DG, Barsh GS, Schwartz MW. Central nervous system control of food intake and body weight. 2006;443:289–295. doi: 10.1038/nature05026. [DOI] [PubMed] [Google Scholar]
  • 2.Spiegelman BM, Flier JS. Obesity and the regulation of energy balance. Cell. 2001;104:531–543. doi: 10.1016/s0092-8674(01)00240-9. [DOI] [PubMed] [Google Scholar]
  • 3.Williams G, Harrold JA, Cutler DJ. The hypothalamus and the regulation of energy homeostasis: lifting the lid on a black box. Proc Nutr Soc. 2000;59:385–396. doi: 10.1017/s0029665100000434. [DOI] [PubMed] [Google Scholar]
  • 4.Ikeda A, Nishina PM, Naggert JK. The tubby-like proteins, a family with roles in neuronal development and function. J Cell Sci. 2002;115:9–14. doi: 10.1242/jcs.115.1.9. [DOI] [PubMed] [Google Scholar]
  • 5.Sahly I, Gogat K, Kobetz A, Marchant D, Menasche M, et al. Prominent neuronal-specific tub gene expression in cellular targets of tubby mice mutation. Hum Mol Genet. 1998;7:1437–1447. doi: 10.1093/hmg/7.9.1437. [DOI] [PubMed] [Google Scholar]
  • 6.Kleyn PW, Fan W, Kovats SG, Lee JJ, Pulido JC, et al. Identification and characterization of the mouse obesity gene tubby: a member of a novel gene family. Cell. 1996;85:281–290. doi: 10.1016/s0092-8674(00)81104-6. [DOI] [PubMed] [Google Scholar]
  • 7.Coleman DL, Eicher EM. Fat (fat) and tubby (tub): two autosomal recessive mutations causing obesity syndromes in the mouse. J Hered. 1990;81:424–427. doi: 10.1093/oxfordjournals.jhered.a111019. [DOI] [PubMed] [Google Scholar]
  • 8.Backberg M, Madjid N, Ogren SO, Meister B. Down-regulated expression of agouti-related protein (AGRP) mRNA in the hypothalamic arcuate nucleus of hyperphagic and obese tub/tub mice. Brain Res Mol Brain Res. 2004;125:129–139. doi: 10.1016/j.molbrainres.2004.03.012. [DOI] [PubMed] [Google Scholar]
  • 9.Guan XM, Yu H, Van der Ploeg LH. Evidence of altered hypothalamic pro-opiomelanocortin/neuropeptide Y mRNA expression in tubby mice. Brain Res Mol Brain Res. 1998;59:273–279. doi: 10.1016/s0169-328x(98)00150-8. [DOI] [PubMed] [Google Scholar]
  • 10.Wang Y, Seburn K, Bechtel L, Lee BY, Szatkiewicz JP, et al. Defective carbohydrate metabolism in mice homozygous for the tubby mutation. Physiol Genomics. 2006 doi: 10.1152/physiolgenomics.00239.2005. [DOI] [PubMed] [Google Scholar]
  • 11.Nishina PM, North MA, Ikeda A, Yan Y, Naggert JK. Molecular characterization of a novel tubby gene family member, TULP3, in mouse and humans. Genomics. 1998;54:215–220. doi: 10.1006/geno.1998.5567. [DOI] [PubMed] [Google Scholar]
  • 12.Ashrafi K, Chang FY, Watts JL, Fraser AG, Kamath RS, et al. Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes. Nature. 2003;421:268–272. doi: 10.1038/nature01279. [DOI] [PubMed] [Google Scholar]
  • 13.Mukhopadhyay A, Deplancke B, Walhout AJ, Tissenbaum HA. C. elegans tubby regulates life span and fat storage by two independent mechanisms. Cell Metab. 2005;2:35–42. doi: 10.1016/j.cmet.2005.06.004. [DOI] [PubMed] [Google Scholar]
  • 14.Mak HY, Nelson LS, Basson M, Johnson CD, Ruvkun G. Polygenic control of Caenorhabditis elegans fat storage. Nat Genet. 2006;38:363–368. doi: 10.1038/ng1739. [DOI] [PubMed] [Google Scholar]
  • 15.Boggon TJ, Shan WS, Santagata S, Myers SC, Shapiro L. Implication of tubby proteins as transcription factors by structure-based functional analysis. Science. 1999;286:2119–2125. doi: 10.1126/science.286.5447.2119. [DOI] [PubMed] [Google Scholar]
  • 16.Santagata S, Boggon TJ, Baird CL, Gomez CA, Zhao J, et al. G-protein signaling through tubby proteins. Science. 2001;292:2041–2050. doi: 10.1126/science.1061233. [DOI] [PubMed] [Google Scholar]
  • 17.Kapeller R, Moriarty A, Strauss A, Stubdal H, Theriault K, et al. Tyrosine phosphorylation of tub and its association with Src homology 2 domain-containing proteins implicate tub in intracellular signaling by insulin. J Biol Chem. 1999;274:24980–24986. doi: 10.1074/jbc.274.35.24980. [DOI] [PubMed] [Google Scholar]
  • 18.Shiri-Sverdlov R, Custers A, van Vliet-Ostaptchouk JV, van Gorp PJ, Lindsey PJ, et al. Identification of TUB as a novel candidate gene influencing body weight in humans. Diabetes. 2006;55:385–389. doi: 10.2337/diabetes.55.02.06.db05-0997. [DOI] [PubMed] [Google Scholar]
  • 19.Boker LK, van Noord PA, van der Schouw YT, Koot NV, Bueno de Mesquita HB, et al. Prospect-EPIC Utrecht: study design and characteristics of the cohort population. European Prospective Investigation into Cancer and Nutrition. Eur J Epidemiol. 2001;17:1047–1053. doi: 10.1023/a:1020009325797. [DOI] [PubMed] [Google Scholar]
  • 20.Ocke MC, Bueno-de-Mesquita HB, Pols MA, Smit HA, van Staveren WA, et al. The Dutch EPIC food frequency questionnaire. II. Relative validity and reproducibility for nutrients. Int J Epidemiol. 1997;26(Suppl 1):S49–58. doi: 10.1093/ije/26.suppl_1.s49. [DOI] [PubMed] [Google Scholar]
  • 21.Liu S, Willett WC, Stampfer MJ, Hu FB, Franz M, et al. A prospective study of dietary glycemic load, carbohydrate intake, and risk of coronary heart disease in US women. Am J Clin Nutr. 2000;71:1455–1461. doi: 10.1093/ajcn/71.6.1455. [DOI] [PubMed] [Google Scholar]
  • 22.Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics. 2005;21:263–265. doi: 10.1093/bioinformatics/bth457. [DOI] [PubMed] [Google Scholar]
  • 23.Castillo M, Mulet J, Gutierrez LM, Ortiz JA, Castelan F, et al. Role of the RIC-3 protein in trafficking of serotonin and nicotinic acetylcholine receptors. J Mol Neurosci. 2006;30:153–156. doi: 10.1385/JMN:30:1:153. [DOI] [PubMed] [Google Scholar]
  • 24.Stubdal H, Lynch CA, Moriarty A, Fang Q, Chickering T, et al. Targeted deletion of the tub mouse obesity gene reveals that tubby is a loss-of-function mutation. Mol Cell Biol. 2000;20:878–882. doi: 10.1128/mcb.20.3.878-882.2000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Giannaccini G, Giusti L, Santini F, Marsili A, Betti L, et al. Tubby protein in human lymphocytes from normal weight and obese subjects. Clin Biochem. 2007;40:806–809. doi: 10.1016/j.clinbiochem.2007.03.020. [DOI] [PubMed] [Google Scholar]
  • 26.Kretsch MJ, Fong AK, Green MW. Behavioral and body size correlates of energy intake underreporting by obese and normal-weight women. J Am Diet Assoc. 1999;99:300–306; quiz 307–308. doi: 10.1016/S0002-8223(99)00078-4. [DOI] [PubMed] [Google Scholar]
  • 27.Prentice AM, Black AE, Coward WA, Davies HL, Goldberg GR, et al. High levels of energy expenditure in obese women. Br Med J (Clin Res Ed) 1986;292:983–987. doi: 10.1136/bmj.292.6526.983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Lichtman SW, Pisarska K, Berman ER, Pestone M, Dowling H, et al. Discrepancy between self-reported and actual caloric intake and exercise in obese subjects. N Engl J Med. 1992;327:1893–1898. doi: 10.1056/NEJM199212313272701. [DOI] [PubMed] [Google Scholar]
  • 29.Rankinen T, Bouchard C. Genetics of food intake and eating behavior phenotypes in humans. Annu Rev Nutr. 2006;26:413–434. doi: 10.1146/annurev.nutr.26.061505.111218. [DOI] [PubMed] [Google Scholar]
  • 30.Reed DR, Bachmanov AA, Beauchamp GK, Tordoff MG, Price RA. Heritable variation in food preferences and their contribution to obesity. Behav Genet. 1997;27:373–387. doi: 10.1023/a:1025692031673. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.de Castro JM. Genetic influences on daily intake and meal patterns of humans. Physiol Behav. 1993;53:777–782. doi: 10.1016/0031-9384(93)90188-l. [DOI] [PubMed] [Google Scholar]
  • 32.Bray GA. Peptides affect the intake of specific nutrients and the sympathetic nervous system. Am J Clin Nutr. 1992;55:265S–271S. doi: 10.1093/ajcn/55.1.265s. [DOI] [PubMed] [Google Scholar]
  • 33.Fumeron F, Betoulle D, Aubert R, Herbeth B, Siest G, et al. Association of a functional 5-HT transporter gene polymorphism with anorexia nervosa and food intake. Mol Psychiatry. 2001;6:9–10. doi: 10.1038/sj.mp.4000824. [DOI] [PubMed] [Google Scholar]
  • 34.Herbeth B, Aubry E, Fumeron F, Aubert R, Cailotto F, et al. Polymorphism of the 5-HT2A receptor gene and food intakes in children and adolescents: the Stanislas Family Study. Am J Clin Nutr. 2005;82:467–470. doi: 10.1093/ajcn.82.2.467. [DOI] [PubMed] [Google Scholar]
  • 35.Aubert R, Betoulle D, Herbeth B, Siest G, Fumeron F. 5-HT2A receptor gene polymorphism is associated with food and alcohol intake in obese people. Int J Obes Relat Metab Disord. 2000;24:920–924. doi: 10.1038/sj.ijo.0801253. [DOI] [PubMed] [Google Scholar]
  • 36.Loos RJ, Rankinen T, Rice T, Rao DC, Leon AS, et al. Two ethnic-specific polymorphisms in the human Agouti-related protein gene are associated with macronutrient intake. Am J Clin Nutr. 2005;82:1097–1101. doi: 10.1093/ajcn/82.5.1097. [DOI] [PubMed] [Google Scholar]
  • 37.Gorwood P, Kipman A, Foulon C. The human genetics of anorexia nervosa. Eur J Pharmacol. 2003;480:163–170. doi: 10.1016/j.ejphar.2003.08.103. [DOI] [PubMed] [Google Scholar]
  • 38.Berthoud HR. Multiple neural systems controlling food intake and body weight. Neurosci Biobehav Rev. 2002;26:393–428. doi: 10.1016/s0149-7634(02)00014-3. [DOI] [PubMed] [Google Scholar]
  • 39.Wynne K, Stanley S, McGowan B, Bloom S. Appetite control. J Endocrinol. 2005;184:291–318. doi: 10.1677/joe.1.05866. [DOI] [PubMed] [Google Scholar]
  • 40.Leibowitz SF, Wortley KE. Hypothalamic control of energy balance: different peptides, different functions. Peptides. 2004;25:473–504. doi: 10.1016/j.peptides.2004.02.006. [DOI] [PubMed] [Google Scholar]
  • 41.Koegler FH, Schaffhauser RO, Mynatt RL, York DA, Bray GA. Macronutrient diet intake of the lethal yellow agouti (Ay/a) mouse. Physiol Behav. 1999;67:809–812. doi: 10.1016/s0031-9384(99)00104-3. [DOI] [PubMed] [Google Scholar]
  • 42.Hagan MM, Rushing PA, Benoit SC, Woods SC, Seeley RJ. Opioid receptor involvement in the effect of AgRP- (83-132) on food intake and food selection. Am J Physiol Regul Integr Comp Physiol. 2001;280:R814–821. doi: 10.1152/ajpregu.2001.280.3.R814. [DOI] [PubMed] [Google Scholar]
  • 43.Rodgers RJ, Ishii Y, Halford JC, Blundell JE. Orexins and appetite regulation. Neuropeptides. 2002;36:303–325. doi: 10.1016/s0143-4179(02)00085-9. [DOI] [PubMed] [Google Scholar]
  • 44.Ma Y, Olendzki B, Chiriboga D, Hebert JR, Li Y, et al. Association between dietary carbohydrates and body weight. Am J Epidemiol. 2005;161:359–367. doi: 10.1093/aje/kwi051. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Lau C, Toft U, Tetens I, Richelsen B, Jorgensen T, et al. Association between dietary glycemic index, glycemic load, and body mass index in the Inter99 study: is underreporting a problem? Am J Clin Nutr. 2006;84:641–645. doi: 10.1093/ajcn/84.3.641. [DOI] [PubMed] [Google Scholar]
  • 46.Hare-Bruun H, Flint A, Heitmann BL. Glycemic index and glycemic load in relation to changes in body weight, body fat distribution, and body composition in adult Danes. Am J Clin Nutr. 2006;84:871–879; quiz 952–873. doi: 10.1093/ajcn/84.4.871. [DOI] [PubMed] [Google Scholar]
  • 47.McMillan-Price J, Petocz P, Atkinson F, O'Neill K, Samman S, et al. Comparison of 4 diets of varying glycemic load on weight loss and cardiovascular risk reduction in overweight and obese young adults: a randomized controlled trial. Arch Intern Med. 2006;166:1466–1475. doi: 10.1001/archinte.166.14.1466. [DOI] [PubMed] [Google Scholar]
  • 48.Livesey G. Low-glycaemic diets and health: implications for obesity. Proc Nutr Soc. 2005;64:105–113. doi: 10.1079/pns2004400. [DOI] [PubMed] [Google Scholar]
  • 49.Willett W. New York, NY: Simon & Schuster Source; 2001. Eat, drink, and be healthy: the Harvard Medical School guide to healthy eating. [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Figure S1

Detailed picture of TUB gene and it's 3′ flanking region and the location of all SNPs currently to be found in HapMap in this region (http://www.hapmap.org). The pairwise linkage disequilibrium (LD) plot, calculated as r2, among SNPs is shown, with red colour indicating increasing level of LD as measured by D'. The red boxes indicate SNPs genotyped in this study.

(11.07 MB EPS)

Click here for additional data file. (10.6MB, eps)

Articles from PLoS ONE are provided here courtesy of PLOS

RESOURCES