Abstract
Distal hereditary motor neuropathies (dHMN) are a group of rare hereditary neuromuscular disorders characterized by an atrophy that affects peroneal muscles in the absence of sensory symptoms. To date, 23 genes are thought to be responsible for dHMN, four of which encode chaperones: DNAJB2, which encodes a member of the HSP40/DNAJ co-chaperone family; and HSPB1, HSPB3, and HSPB8, encoding three members of the small heat shock protein family. While around 30 different mutations in HSPB1 have been identified, the remaining three genes are altered in many fewer cases. Indeed, a mutation of HSPB3 has only been described in one case, whereas a few cases have been reported carrying mutations in DNAJB2 and HSPB8, most of them caused by a founder c.352+1G>A mutation in DNAJB2 and by mutations affecting the K141 residue in the HSPB8 chaperone. Hence, their rare occurrence makes it difficult to understand the pathological mechanisms driven by such mutations in this neuropathy. Chaperones can assemble into multi-chaperone complexes that form an integrated chaperone network within the cell. Such complexes fulfill relevant roles in a variety of processes, such as the correct folding of newly synthesized proteins, in which chaperones escort them to precise cellular locations, and as a response to protein misfolding, which includes the degradation of proteins that fail to refold properly. Despite this range of functions, mutations in some of these chaperones lead to diseases with a similar clinical profile, suggesting common pathways. This review provides an overview of the genetics of those dHMNs that share a common disease mechanism and that are caused by mutations in four genes encoding chaperones: DNAJB2, HSPB1, HSPB3, and HSPB8.
Keywords: Distal hereditary motor neuropathy, distal spinal muscular atrophy, DNAJB2, HSPB1, HSPB3, Chaperone, Heat shock protein
Chaperones and chaperonopathies
Chaperones (Hartl et al., 2011; Smith et al., 2015) are proteins that, together with the protein degradation machinery (proteasomes, macroautophagy, etc.), contribute to the quality control apparatus and to the proteostasis of a cell. Typically, chaperones recognize other proteins (usually called their clients) to assist in their folding so that they attain their functional conformation at the sites where they must act. Most chaperones are promiscuous and they bind to many clients, although others (dedicated chaperones) restrict their associations to one or a few proteins. However, the information available on the molecules that interact with specific chaperones is still incomplete.
Chaperones also participate in other important processes, such as: (i) the reversion of erroneous folding of newly synthesized proteins; (ii) the prevention of the formation of improper protein aggregates and their disassembly; (iii) the escorting of proteins to their functional sites, including translocation across membranes and the assembly of functional protein-protein, protein-DNA or protein-RNA complexes; and (iv) the sequestering of proteins that are damaged or unable to fold properly to the intracellular protein degradation machinery for destruction. Most of these processes require energy and, therefore, some chaperones have ATP-binding sites and ATPase activity (e.g., Hsp90, Hsp70). By contrast, ATP-independent chaperones must cooperate with the former to carry out such functions. In fact, chaperones tend to assemble into synergistic multi-chaperone complexes of distinct sizes, containing chaperones from the same or different families, as well as other proteins that assist them in their functions, thereby forming an integrated chaperone network in the cell.
Chaperones can either be constitutively expressed, induced by stress (usually but not exclusively, heat shock) or both. Most chaperones induced by heat shock are frequently called heat shock proteins (HSPs). Chaperones, including HSPs, are sometimes classified into six major families according to their molecular mass, although a gross distinction is made between the larger (e.g., the Hsp100, Hsp90, Hsp70, Hsp60, and Hsp40 co-chaperones) and smaller (sHsp, 12–43 kDa, although the vast majority are 30 kDa or less) chaperones. Each group comprises various chaperones and in the human genome, for example, 10 different chaperones have been identified in the sHsp family (HspB1-HspB10). Thus, and although the total number of chaperones in humans is still expanding, an up to date and conservative estimate of their total number would be about 100 genes (Kakkar et al., 2014). Of course, these genes give rise to a much larger number of proteins due to the different transcriptional, translational and post-translational events and modifications they are subjected to. Given the range of activities undertaken by chaperones and the vast number of multimeric complexes that they form with other chaperones, some functional redundancies are likely to exist in their extended networks. Therefore, a single chaperone, or even of a group of dedicated chaperones, would not be expected to be exclusively responsible for a specific task with a particular client, and defects in one chaperone can usually be compensated by others, albeit more or less successfully. Together with the possible lethality associated with the loss of some important chaperones, this redundancy might explain the relatively low number of diseases known to be produced by mutations in genes encoding chaperones (Macario and Conway de Macario, 2007; Kakkar et al., 2014).
Proteopathies and chaperonopathies
There are many disorders, some that are well known, in which specific misfolded proteins aggregate and accumulate in cells (Walker et al., 2006). Classical examples are Huntington's, Parkinson's and Alzheimer's diseases, although they are not primarily due to defects in the machinery that assist proteins to fold properly but rather, to defects in the specific proteins that accumulate in each disease (e.g., huntingtin, alpha-synuclein, amyloid-beta peptide, and tau). Therefore, these diseases can be referred to as proteopathies or proteinopathies and in principle, they are not considered to be chaperonopathies.
Nevertheless, genetic or post-transcriptional defects in chaperones may be pathological given their role in protein folding. In fact, and despite the potential functional redundancy of chaperones, mutations in genes encoding these proteins have been associated with various disorders that can be collectively referred to as chaperonopathies (Macario and Conway de Macario, 2007). These mutations can affect different yet important domains of a chaperone (e.g., the ATP binding site, client recognition site, sites for interaction with other chaperones, etc.), but they can also affect other sites regulating the expression or the activity of the chaperone. The role of chaperones implies that chaperonopathies may be associated with the aggregation of misfolded proteins but, as mentioned above, such diseases differ from proteinopathies with respect to the protein that is altered (either chaperones or other proteins).
The growing list of chaperones involved in distal hereditary motor neuropathies
Distal hereditary motor neuropathies (dHMN) or distal spinal muscular atrophies (dSMA) are a group of rare hereditary neuromuscular disorders characterized by an atrophy that affects peroneal muscles in the absence of sensory symptoms (Harding, 1993). Classically, patients experience progressive distal weakness and atrophy affecting the lower limbs, which subsequently spreads to the proximal muscles and ultimately reaches the upper limbs as the disease progresses, with the possible appearance of foot deformities. Other additional manifestations include ataxia or pyramidal tract signs, although these are unusual. These symptoms contrast with those of Charcot-Marie-Tooth disease (CMT) or hereditary motor sensory neuropathy (HMSN), conditions in which sensory involvement is also evident. However, there are some forms of CMT, in particular in axonal CMT or CMT type 2 (CMT2), in which only minor sensory involvement is recognized, and it is difficult to distinguish dHMN from CMT2 (Harding and Thomas, 1980). In fact, some genetic overlap is observed in CMT and dHMN as both conditions can be caused by mutations in the same gene, and even by the same mutation.
To date 23 genes associated with dHMN have been reported (Neuromuscular Disease Center, http://neuromuscular.wustl.edu/synmot.html), although no molecular diagnosis is available in most dHMN patients (Rossor et al., 2012a). Distinct activities are affected in motor-nerve disease, including: protein folding/misfolding (HSPB1, HSPB3, HSPB8, DNAJB2, and BSCL2), RNA metabolism (IGHMBP2, SETX, and GARS), axonal transport (DYNC1H1, DCTN1), cation channel activity (ATP7A, TRPV4), transcriptional control (FBXO38), etc. Here we will focus exclusively on dHMNs that involve mutations in the chaperone genes HSPB1, HSPB8, DNAJB2, and HSPB3, all four encoding ATP-independent chaperones. Although, compensatory mechanisms driven by the relationships and redundancies within the chaperome can overcome specific chaperone defects, this does not appear to be the case here, as in other diseases. Indeed, even when this compensation occurs, the chaperone activity associated to the defective chaperones would be modified considerably.
The DNAJB2/HSJ1 gene is a member of the HSP40/DNAJ co-chaperone family, characterized by a highly conserved domain of about 70 amino acids, the J domain. This domain allows proteins of this family to interact with Hsp70, and to regulate its ATPase-dependent activity in protein folding and in protein complex dissociation (Hageman et al., 2010). Moreover, spliced transcript variants have been described for the DNAJB2 gene that encode different isoforms, one of which, DNAJB2a, participates in the resolution of protein aggregates associated with important neurodegenerative diseases (Chen et al., 2016 and references cited therein). Although this protein is mainly expressed in the brain, it has also been localized in normal and diseased skeletal muscle, where it is thought to influence protein turnover through the ubiquitin-proteasome pathway (Claeys et al., 2010). DNAJB2 interacts with ubiquitin chains and their fusion proteins, and since the proteasome mediates the degradation of selected proteins, it is possible that some of these proteins are related to the cytoskeleton (microtubules, intermediate filaments, and microfilaments), in accordance with the role of the other chaperones involved in dHMN (see below).
There are 10 cases where autosomal recessive inheritance has been associated to mutations in the DNAJB2 gene (Table 1). The first mutation was reported in homozygosis, DNAJB2 c.352+1G>A, and it was identified in a Moroccan family with a dHMN phenotype (dHMN5) by genome wide mapping (Blumen et al., 2012). In this case, the expression of DNAJB2 was dampened in fibroblasts from the patients and overexpression of the protein reduced the formation of inclusions in a neuronal cellular model, suggesting DNAJB2 is active in motor neurons and/or muscle (Blumen et al., 2012). Two additional homozygous mutations were later described in the DNAJB2 gene, c.229+1G>A and c.14A>G (p.Y5C), in a family diagnosed with dHMN (dHMN5) and another with CMT2 (CMT2T), respectively (Gess et al., 2014). More recently, a homozygous large deletion was reported in a family with spinal muscular atrophy and parkinsonism, broadening the clinical spectrum of DNAJB2 related neuropathies (Sanchez et al., 2016).
Table 1.
Gene | HGVS (nucleotide) | HGVS (protein) | Disease/Phenotype | References |
---|---|---|---|---|
DNAJB2 | c.352+1G>A | donor site | dHMN/CMT2 | Blumen et al., 2012; Frasquet et al., 2016; Lupo et al., 2016 |
c.229+1G>A | donor site | dHMN | Gess et al., 2014 | |
c.14A>G | p.Y5C | dHMN | Gess et al., 2014 | |
HSPB1 | c.20C>G | p.P7R | CMT2 | Luigetti et al., 2010 |
c.45C>A | p.S15R | Peripheral neuropathy | Antoniadi et al., 2015 | |
c.100G>A | p.G34R | HMSN | Capponi et al., 2011; Muranova et al., 2015 | |
c.116C>T | p.P39L | dHMN/CMT2 | Houlden et al., 2008; Muranova et al., 2015; Yavarna et al., 2015 | |
c.121G>A | p.E41K | dHMN | Capponi et al., 2011; Muranova et al., 2015 | |
c.250G>A | p.G84R | CMT2 | Manganelli et al., 2014 | |
c.250G>C | p.G84R | dHMN | James et al., 2008; Fischer et al., 2012; Nefedova et al., 2015 | |
c.257C>T | p.S86L | dHMN/ALS | Scarlato et al., 2015 | |
c.295C>A | p.L99M | dHMN/CMT2 | Houlden et al., 2008; Nefedova et al., 2015 | |
c.380G>T | p.R127L | CMT2 | Hoyer et al., 2014; Ylikallio et al., 2015 | |
c.379C>T | p.R127W | dHMN | Evgrafov et al., 2004; Almeida-Souza et al., 2011 | |
c.404C>G | p.S135C | CMT2 | Benedetti et al., 2010; Oberstadt et al., 2016 | |
c.404C>G | p.S135C | CMT2 | Benedetti et al., 2010; Oberstadt et al., 2016 | |
c.404C>T | p.S135F | CMT2 | Evgrafov et al., 2004; Almeida-Souza et al., 2010, 2011 | |
c.404C>A | p.S135Y | CMT2 | Ylikallio et al., 2014 | |
c.407G>T | p.R136L | dHMN/CMT2 | Capponi et al., 2011; Gaeta et al., 2012; Stancanelli et al., 2015 | |
c.406C>T | p.R136W | CMT2 | Evgrafov et al., 2004; Almeida-Souza et al., 2010, 2011 | |
c.418C>G | p.R140G | dHMN/CMT2 | Houlden et al., 2008; Nefedova et al., 2015 | |
c.421A>C | p.K141Q | dHMN | Ikeda et al., 2009; Nefedova et al., 2013; Maeda et al., 2014 | |
c.452C>T | p.T151I | dHMN | Evgrafov et al., 2004; Almeida-Souza et al., 2010, 2011 | |
c.490A>G | p.T164A | CMT2 | Lin et al., 2011 | |
c.523C>T | p.Q175X | CMT2 | Rossor et al., 2012b | |
c.539C>T | p.T180I | dHMN/CMT2 | Luigetti et al., 2010 | |
c.545C>T | p.P182L | dHMN | Evgrafov et al., 2004; Almeida-Souza et al., 2010, 2011 | |
c.544C>T | p.P182S | dHMN | Kijima et al., 2005 | |
c.562C>T | p.R188W | CMT2 | Capponi et al., 2011 | |
c.365-13C>T | acceptor site | CMT2 | Benedetti et al., 2010 | |
c.-217T>C | regulatory | ALS | Dierick et al., 2007 | |
c.476_477delCT | p.P159RfsX41 | Peripheral neuropathy, early onset | Mandich et al., 2010; Capponi et al., 2011 | |
c.505delA | p.M169CfsX4 | CMT | DiVincenzo et al., 2014 | |
c.171_172insGCGCCCT | p.L58AfsX105 | CMT | DiVincenzo et al., 2014 | |
HSPB3 | c.21G>T | p.R7S | dHMN | Kolb et al., 2010 |
HSPB8 | c.423G>C) | p.L141N | dHMN/CMT2 | Irobi et al., 2004 |
c.421A>G | p.L141E | dHMN | Irobi et al., 2004 | |
c.423G>T | p.L141N | CMT2 | Tang B. S. et al., 2005 | |
c.422A>C | p.L141T | CMT2 | Nakhro et al., 2013 | |
c.151insC | p.P173SfsX43 | Distal myopathy/dHMN | Ghaoui et al., 2016 |
ALS, Amyotrophic lateral sclerosis; CMT2, Charcot-Marie-Tooth disease type 2 or axonal; dHMN, Distal hereditary motor neuropathy; HMSN, hereditary motor and sensory neuropathy.
To date, the remaining known patients with mutations in the DNAJB2 gene carry the c.352+1G>A mutation in homozygosis: 5 families from Spain (Frasquet et al., 2016; Lupo et al., 2016) and one from Brazil (Teive et al., 2015). These Spanish families were investigated by haplotype analysis and they carried the same homozygous haplotype. Hence, the DNAJB2 c.352+1G>A mutation appears to be a founder event (Lupo et al., 2016), and it is shared with a family reported elsewhere (Blumen et al., 2012). The patients in Spain displayed a dHMN or CMT2 phenotype and, in some cases, initial clinical manifestations that were consistent with dHMN and that subsequently evolved to CMT2 (Frasquet et al., 2016). Moreover, the peripheral motor neuropathy recently described in a Brazilian family carrying the DNAJB2 c.352+1G>A mutation was associated with parkinsonism and cerebellar ataxia (Teive et al., 2015). Some patients show parkinsonian symptoms (Frasquet et al., 2016; Sanchez et al., 2016; Teive et al., 2015), which probably are due to the DNAJB2 mutations. Other additional symptoms such as cerebellar ataxia may be coincidental. Further studies of a larger analytical series will be necessary to define the clinical manifestations associated with DNAJB2 mutations in more depth.
HSPB1, HSPB3, and HSPB8 are the three other chaperones associated with dHMNs, and they are all members of the sHsp family. These proteins are characterized by a highly conserved α-crystallin domain that is related to their chaperone activity, which is more closely associated with an 80–100 amino acid domain in the C- rather than the N-terminal region of the protein (Nefedova et al., 2015). These chaperones are normally found as monomers, but under stress, they tend to also interact with each other to form large, labile homo- and hetero-oligomeric complexes of more than twenty identical or different subunits, driving their recognition and interaction with new protein clients (Arrigo, 2013). Certain sHsp are tissue specific, while others are more ubiquitously expressed in function of the tissue and conditions. The main role of sHsps is to carry their denatured clients to ATP-dependent chaperones for renaturation or to the cell's protein degradation machinery (proteasomes and autophagosomes). In terms of dHMN and HMSN, sHsps stabilize the activities of the cell cytoskeleton, interacting with most of its proteins components, as well as preventing oxidative stress (Nefedova et al., 2015).
Autosomal dominant mutations in the HSPB1/HSP27 gene were first described in four families with dHMN (dHMN2B) and in one family with CMT2 (CMT2F) (Evgrafov et al., 2004). More than 30 different mutations causing dHMN or CMT2 have since been described in the HSPB1 gene, some of which also produce other manifestations (Table 1; Evgrafov et al., 2004; Kijima et al., 2005; Tang B. et al., 2005; Chung et al., 2008; Houlden et al., 2008; James et al., 2008; Ikeda et al., 2009; Luigetti et al., 2010; Mandich et al., 2010; Solla et al., 2010; Murphy et al., 2012; Rossor et al., 2012b; Sivera et al., 2013; Ylikallio et al., 2014, 2015). An autosomal recessive mutation in the HSPB1 gene was identified in a consanguineous family with a similar clinical profile (Houlden et al., 2008). On the whole, HSPB1 mutations are inherited dominantly and while most involve a change in one codon, they may also produce a frameshift or premature stop codons. The protein encoded by this gene is ubiquitously expressed and it is induced by environmental stress, translocating from the cytoplasm to the nucleus to influence stress resistance and produce other changes. The known mutations are located in all three domains of the protein: N-terminus, α-crystallin and C-terminus. These HSPB1 mutations mostly modify the oligomeric state of the protein, usually negatively but also positively (certain mutations in the α-crystallin domain), altering its chaperone activity and in both cases affecting normal cytoskeletal function. HSPB1 is involved in the organization of the neurofilament network, which is important to maintain the axonal cytoskeleton and transport, and indeed, overexpression of HSPB1 mutants produces protein aggregates and altered neurofilament transport in the axon (Evgrafov et al., 2004; Ackerley et al., 2006; Zhai et al., 2007). Thus, an increased interaction with tubulin and an enhanced stability of the microtubule network has been observed for some mutants (Almeida-Souza et al., 2011). Moreover, there are severe defects in axon transport in transgenic mice expressing human mutant HSPB1 in neurons due to a decrease in acetylated α-tubulin (d'Ydewalle et al., 2011). As a result, inhibitors of histone deacetylase 6 (HDAC6, a client of HSPB1 that acetylates α-tubulin) have successfully reversed the axonal loss in a mouse model of CMT2F that expresses mutant HSPB1 (d'Ydewalle et al., 2011). HSPB1 is also involved in a variety of human diseases, such as cancer, Alzheimer's disease and heart disease (Sun and MacRae, 2005).
At present, only one family is thought to carry clinical mutations in the HSPB3/HSPL27 gene: a missense mutation c.21G>T (p.R7S) described in two affected sisters who suffer from dHMN (dHMN2C) (Table 1; Kolb et al., 2010). The function of HSPB3 is not fully understood, although replacing the positively charged R7 residue with a neutral polar amino acid would affect its structure and therefore, its proprieties. In contrast to the ubiquitous expression of HSPB1 and HSPB8, HSPB3 is more tissue specific (heart, brain, skeletal and smooth muscle) and it is expressed strongly in muscle (Sugiyama et al., 2000). HSPB3 interacts with HSPB2 and these two proteins in turn both interact with HSPB8, potentially contributing to maintain myofibril integrity (Fontaine et al., 2005). Finally, HSPB3 and HSPB2 are upregulated in a mouse model for spinal and bulbar muscular atrophy (SBMA), an inherited motoneuron disease (Rusmini et al., 2015).
Mutations in the HSPB8/HSP22 gene were first associated with dHMN (dHMN2A) (Irobi et al., 2004) and later, with CMT2 (CMT2L) (Table 1; Tang B. S. et al., 2005). Four mutations have been described and they all affect position K141: c.423G>T/c.423G>C (p.K141N), c.421A>G (p.K141E), and c.422A>C (p.K141T). These mutations are all transmitted in an autosomal dominant fashion (Irobi et al., 2004; Tang B. S. et al., 2005; Nakhro et al., 2013), and this hot-spot residue is located in a hydrophobic strand of the α-crystallin domain. The mutations eliminate the positive charge of the K41 amino acid, which will affect the interactions of HSPB8 with other sHsps like HSPB27, HSPB3, and HSPB2 (Irobi et al., 2004; Fontaine et al., 2006; Kasakov et al., 2007; Nakhro et al., 2013). Mutational screening in a large clinical series revealed additional patients but no novel mutations associated with dHMN or CMT2 (Dierick et al., 2008; Sivera et al., 2013; Fridman et al., 2015). However, two mutations, c.421A>G (p.K141E), and c.151insC (p.P173SfsX43) were recently described in two unrelated families with a new distal neuromyopathy phenotype, expanding the clinical phenotype associated with HSPB8 (Ghaoui et al., 2016).
HSPB8 is ubiquitously expressed (particularly strongly in the spinal cord, and especially in motor and sensory neurons), and it acts as a chaperone and a regulator of apoptosis (Shemetov et al., 2008). HspB8 acts as a chaperone in association with the co-chaperones Bag3 and Stub1, stimulating chaperone-assisted selective macroautophagy in muscle to maintain the actin cytoskeleton (Arndt et al., 2010). Expression of HSPB8 mutants in cell models promotes the formation of intracellular aggregates and it augments cell death (Benn et al., 2002; Irobi et al., 2004). These protein aggregates are also observed in fibroblasts from patients who carry HSPB8 mutations, and they are coupled to a decrease in mitochondrial membrane potential and a reduction in cell viability (Irobi et al., 2012; Vicario et al., 2014). Although the pathological mechanisms underlying these conditions remain enigmatic, specific motor neuron degeneration is associated with HSPB8 mutations (Irobi et al., 2010). In addition, expression of this protein can be induced by estrogen in estrogen receptor-positive breast cancer cells, indicating a role in carcinogenesis, and suggesting the possible involvement of HspB8 in regulating cell proliferation and apoptosis.
Since mutations in these four chaperones, as well as those in other genes, produce a similar pathological phenotype, it would seem obvious that they must share some pathogenic pathways. It has been proposed that most, if not all, of the proteins affected in dHMN/CMT2 are related with the impaired axonal trafficking of cell components (Bucci et al., 2012; Gentil and Cooper, 2012). Considering the activity of all the chaperones described above, it appears that mutations in all these genes could affect the cytoskeleton, either by interacting with relevant proteins (e.g., in the case of the sHsps) or by regulating their specific degradation (e.g., in the case of DNAJB2 and HspB8). Since the cytoskeleton participates in axonal transport, as well as in the dynamics of various organelles and plasma membrane receptors, there are clear potential relationships with other mutations that cause dHMN/CMT2. To date there are no effective treatments for these diseases and therefore, much more research is needed to understand the consequences of each specific mutation that provokes them. However, one potential therapy to be considered, at least in certain cases of these chaperonopathies, could be to overexpress the chaperone to rescue its defective functions. Indeed, the overexpression of HspB8 ameliorates the accumulation of aggregates associated with the p.P182L mutation in HspB1 (Carra et al., 2010), or the effects on its clients, as illustrated by the use of inhibitors of histone deacetylase 6 to treat CMT2F (d'Ydewalle et al., 2011).
Author contributions
Conceptualization: EK, CE; Writing-draft, review and editing: VL, CA, EK, CE; Funding acquisition and supervision: EK, CE.
Conflict of interest statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
This work was supported by the Instituto de Salud Carlos III (ISCIII) [Grants no. PI12/000453 and PI15/000187 to CE] and by the MINECO [Grant no. SAF2014-54604-C3-2-R to EK]. CE has a “Miguel Servet” contract funded by the ISCIII and the Centro de Investigación Príncipe Felipe (CIPF) [Grant no. CPII14/00002]. CA is supported by the CIBER de Enfermedades Raras (CIBERER)-ISCIII.
References
- Ackerley S., James P. A., Kalli A., French S., Davies K. E., Talbot K. (2006). A mutation in the small heat-shock protein HSPB1 leading to distal hereditary motor neuronopathy disrupts neurofilament assembly and the axonal transport of specific cellular cargoes. Hum. Mol. Genet. 15, 347–354. 10.1093/hmg/ddi452 [DOI] [PubMed] [Google Scholar]
- Almeida-Souza L., Asselbergh B., d'Ydewalle C., Moonens K., Goethals S., de Winter V., et al. (2011). Small heat-shock protein HSPB1 mutants stabilize microtubules in Charcot-Marie-Tooth neuropathy. J. Neurosci. 31, 15320–15328. 10.1523/JNEUROSCI.3266-11.2011 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Almeida-Souza L., Goethals S., de Winter V., Dierick I., Gallardo R., Van Durme J., et al. (2010). Increased monomerization of mutant HSPB1 leads to protein hyperactivity in Charcot-Marie-Tooth neuropathy. J. Biol. Chem. 285, 12778–12786. 10.1074/jbc.M109.082644 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Antoniadi T., Buxton C., Dennis G., Forrester N., Smith D., Lunt P., et al. (2015). Application of targeted multi-gene panel testing for the diagnosis of inherited peripheral neuropathy provides a high diagnostic yield with unexpected phenotype-genotype variability. BMC Med. Genet. 16, 84. 10.1186/s12881-015-0224-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Arndt V., Dick N., Tawo R., Dreiseidler M., Wenzel D., Hesse M., et al. (2010). Chaperone-assisted selective autophagy is essential for muscle maintenance. Curr. Biol. 20, 143–148. 10.1016/j.cub.2009.11.022 [DOI] [PubMed] [Google Scholar]
- Arrigo A. P. (2013). Human small heat shock proteins: protein interactomes of homo- and hetero-oligomeric complexes: an update. FEBS Lett. 587, 1959–1969. 10.1016/j.febslet.2013.05.011 [DOI] [PubMed] [Google Scholar]
- Benedetti S., Previtali S. C., Coviello S., Scarlato M., Cerri F., Di Pierri E., et al. (2010). Analyzing histopathological features of rare Charcot-Marie-Tooth neuropathies to unravel their pathogenesis. Arch. Neurol. 67, 1498–1505. 10.1001/archneurol.2010.303 [DOI] [PubMed] [Google Scholar]
- Benn S. C., Perrelet D., Kato A. C., Scholz J., Decosterd I., Mannion R. J., et al. (2002). Hsp27 upregulation and phosphorylation is required for injured sensory and motor neuron survival. Neuron 36, 45–56. 10.1016/S0896-6273(02)00941-8 [DOI] [PubMed] [Google Scholar]
- Blumen S. C., Astord S., Robin V., Vignaud L., Toumi N., Cieslik A., et al. (2012). A rare recessive distal hereditary motor neuropathy with HSJ1 chaperone mutation. Ann. Neurol. 71, 509–519. 10.1002/ana.22684 [DOI] [PubMed] [Google Scholar]
- Bucci C., Bakke O., Progida C. (2012). Charcot-Marie-Tooth disease and intracellular traffic. Prog. Neurobiol. 99, 191–225. 10.1016/j.pneurobio.2012.03.003 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Capponi S., Geroldi A., Fossa P., Grandis M., Ciotti P., Gulli R., et al. (2011). HSPB1 and HSPB8 in inherited neuropathies: study of an Italian cohort of dHMN and CMT2 patients. J. Peripher. Nerv. Syst. 16, 287–294. 10.1111/j.1529-8027.2011.00361.x [DOI] [PubMed] [Google Scholar]
- Carra S., Boncoraglio A., Kanon B., Brunsting J. F., Minoia M., Rana A., et al. (2010). Identification of the Drosophila ortholog of HSPB8: implication of HSPB8 loss of function in protein folding diseases. J. Biol. Chem. 285, 37811–37822. 10.1074/jbc.M110.127498 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen H. J., Mitchell J. C., Novoselov S., Miller J., Nishimura A. L., Scotter E. L., et al. (2016). The heat shock response plays an important role in TDP-43 clearance: evidence for dysfunction in amyotrophic lateral sclerosis. Brain 139, 1417–1432. 10.1093/brain/aww028 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chung K. W., Kim S. B., Cho S. Y., Hwang S. J., Park S. W., Kang S. H., et al. (2008). Distal hereditary motor neuropathy in Korean patients with a small heat shock protein 27 mutation. Exp. Mol. Med. 40, 304–312. 10.3858/emm.2008.40.3.304 [DOI] [PMC free article] [PubMed] [Google Scholar]
- d'Ydewalle C., Krishnan J., Chiheb D. M., Van Damme P., Irobi J., Kozikowski A. P., et al. (2011). HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1-induced Charcot-Marie-Tooth disease. Nat. Med. 17, 968–974. 10.1038/nm.2396 [DOI] [PubMed] [Google Scholar]
- Claeys K. G., Sozanska M., Martin J. J., Lacene E., Vignaud L., Stockholm D., et al. (2010). DNAJB2 expression in normal and diseased human and mouse skeletal muscle. Am. J. Pathol. 176, 2901–2910. 10.2353/ajpath.2010.090663 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dierick I., Baets J., Irobi J., Jacobs A., De Vriendt E., Deconinck T., et al. (2008). Relative contribution of mutations in genes for autosomal dominant distal hereditary motor neuropathies: a genotype-phenotype correlation study. Brain 131, 1217–1227. 10.1093/brain/awn029 [DOI] [PubMed] [Google Scholar]
- Dierick I., Irobi J., Janssens S., Theuns J., Lemmens R., Jacobs A., et al. (2007). Genetic variant in the HSPB1 promoter region impairs the HSP27 stress response. Hum. Mutat. 28, 830. 10.1002/mgg3.106 [DOI] [PubMed] [Google Scholar]
- DiVincenzo C., Elzinga C. D., Medeiros A. C., Karbassi I., Jones J. R., Evans M. C., et al. (2014). The allelic spectrum of Charcot-Marie-Tooth disease in over 17,000 individuals with neuropathy. Mol. Genet. Genomic Med. 2, 522–529. 10.1002/mgg3.106 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Evgrafov O. V., Mersiyanova I., Irobi J., Van Den Bosch L., Dierick I., Leung C. L., et al. (2004). Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy. Nat. Genet. 36, 602–606. 10.1038/ng1354 [DOI] [PubMed] [Google Scholar]
- Fischer C., Trajanoski S., Papic L., Windpassinger C., Bernert G., Freilinger M., et al. (2012). SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth disease. J. Neurol. 259, 515–523. 10.1007/s00415-011-6213-8 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fontaine J. M., Sun X., Benndorf R., Welsh M. J. (2005). Interactions of HSP22 (HSPB8) with HSP20, alphaB-crystallin, and HSPB3. Biochem. Biophys. Res. Commun. 337, 1006–1011. 10.1016/j.bbrc.2005.09.148 [DOI] [PubMed] [Google Scholar]
- Fontaine J. M., Sun X., Hoppe A. D., Simon S., Vicart P., Welsh M. J., et al. (2006). Abnormal small heat shock protein interactions involving neuropathy-associated HSP22 (HSPB8) mutants. FASEB J. 20, 2168–2170. 10.1096/fj.06-5911fje [DOI] [PubMed] [Google Scholar]
- Frasquet M., Chumillas M. J., Vilchez J. J., Márquez-Infante C., Palau F., Vazquez-Costa J. F., et al. (2016). Phenotype and natural history of inherited neuropathies caused by HSJ1 c.352+1G>A mutation. J. Neurol. Neurosurg. Psychiatry 87, 1265–1268. 10.1136/jnnp-2015-312890 [DOI] [PubMed] [Google Scholar]
- Fridman V., Bundy B., Reilly M. M., Pareyson D., Bacon C., Burns J., et al. (2015). CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis. J. Neurol. Neurosurg. Psychiatr. 86, 873–878. 10.1136/jnnp-2014-308826 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gaeta M., Mileto A., Mazzeo A., Minutoli F., Di Leo R., Settineri N., et al. (2012). MRI findings, patterns of disease distribution, and muscle fat fraction calculation in five patients with Charcot-Marie-Tooth type 2 F disease. Skeletal Radiol. 41, 515–524. 10.1007/s00256-011-1199-y [DOI] [PubMed] [Google Scholar]
- Gentil B. J., Cooper L. (2012). Molecular basis of axonal dysfunction and traffic impairments in CMT. Brain Res. Bull. 88, 444–453. 10.1016/j.brainresbull.2012.05.003 [DOI] [PubMed] [Google Scholar]
- Gess B., Auer-Grumbach M., Schirmacher A., Strom T., Zitzelsberger M., Rudnik-Schoneborn S., et al. (2014). HSJ1-related hereditary neuropathies: novel mutations and extended clinical spectrum. Neurology 83, 1726–1732. 10.1212/WNL.0000000000000966 [DOI] [PubMed] [Google Scholar]
- Ghaoui R., Palmio J., Brewer J., Lek M., Needham M., Evila A., et al. (2016). Mutations in HSPB8 causing a new phenotype of distal myopathy and motor neuropathy. Neurology 86, 391–398. 10.1212/WNL.0000000000002324 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hageman J., Rujano M. A., van Waarde M. A., Kakkar V., Dirks R. P., Govorukhina N., et al. (2010). A DNAJB chaperone subfamily with HDAC-dependent activities suppresses toxic protein aggregation. Mol. Cell 37, 355–369. 10.1016/j.molcel.2010.01.001 [DOI] [PubMed] [Google Scholar]
- Harding A. E. (1993). Peripheral Neuropathy, eds Dyck P. J., Thomas P. K., Griffin J. W., Low P. A., Poduslo J. F. Philadelphia, PA: Saunders Company. [Google Scholar]
- Harding A. E., Thomas P. K. (1980). Genetic aspects of hereditary motor and sensory neuropathy (types I and II). J. Med. Genet. 17, 329–336. 10.1136/jmg.17.5.329 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hartl F. U., Bracher A., Hayer-Hartl M. (2011). Molecular chaperones in protein folding and proteostasis. Nature 475, 324–332. 10.1038/nature10317 [DOI] [PubMed] [Google Scholar]
- Houlden H., Laura M., Wavrant-De Vrieze F., Blake J., Wood N., Reilly M. M. (2008). Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2. Neurology 71, 1660–1668. 10.1212/01.wnl.0000319696.14225.67 [DOI] [PubMed] [Google Scholar]
- Høyer H., Braathen G. J., Busk Ø. L., Holla Ø. L., Svendsen M., Hilmarsen H. T., et al. (2014). Genetic diagnosis of Charcot-Marie-Tooth disease in a population by next-generation sequencing. Biomed. Res. Int. 2014:210401. 10.1155/2014/210401 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ikeda Y., Abe A., Ishida C., Takahashi K., Hayasaka K., Yamada M. (2009). A clinical phenotype of distal hereditary motor neuronopathy type II with a novel HSPB1 mutation. J. Neurol. Sci. 277, 9–12. 10.1016/j.jns.2008.09.031 [DOI] [PubMed] [Google Scholar]
- Irobi J., Almeida-Souza L., Asselbergh B., De Winter V., Goethals S., Dierick I., et al. (2010). Mutant HSPB8 causes motor neuron-specific neurite degeneration. Hum. Mol. Genet. 19, 3254–3265. 10.1093/hmg/ddq234 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Irobi J., Holmgren A., De Winter V., Asselbergh B., Gettemans J., Adriaensen D., et al. (2012). Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients. Neuromuscul. Disord. 22, 699–711. 10.1016/j.nmd.2012.04.005 [DOI] [PubMed] [Google Scholar]
- Irobi J., Van Impe K., Seeman P., Jordanova A., Dierick I., Verpoorten N., et al. (2004). Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy. Nat. Genet. 36, 597–601. 10.1038/ng1328 [DOI] [PubMed] [Google Scholar]
- James P. A., Rankin J., Talbot K. (2008). Asymmetrical late onset motor neuropathy associated with a novel mutation in the small heat shock protein HSPB1 (HSP27). J. Neurol. Neurosurg. Psychiatr. 79, 461–463. 10.1136/jnnp.2007.125179 [DOI] [PubMed] [Google Scholar]
- Kakkar V., Meister-Broekema M., Minoia M., Carra S., Kampinga H. H. (2014). Barcoding heat shock proteins to human diseases: looking beyond the heat shock response. Dis. Model. Mech. 7, 421–434. 10.1242/dmm.014563 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kasakov A. S., Bukach O. V., Seit-Nebi A. S., Marston S. B., Gusev N. B. (2007). Effect of mutations in the beta5-beta7 loop on the structure and properties of human small heat shock protein HSP22 (HspB8, H11). FEBS J. 274, 5628–5642. 10.1111/j.1742-4658.2007.06086.x [DOI] [PubMed] [Google Scholar]
- Kijima K., Numakura C., Goto T., Takahashi T., Otagiri T., Umetsu K., et al. (2005). Small heat shock protein 27 mutation in a Japanese patient with distal hereditary motor neuropathy. J. Hum. Genet. 50, 473–476. 10.1007/s10038-005-0280-6 [DOI] [PubMed] [Google Scholar]
- Kolb S. J., Snyder P. J., Poi E. J., Renard E. A., Bartlett A., Gu S., et al. (2010). Mutant small heat shock protein B3 causes motor neuropathy: utility of a candidate gene approach. Neurology 74, 502–506. 10.1212/WNL.0b013e3181cef84a [DOI] [PubMed] [Google Scholar]
- Lin K. P., Soong B. W., Yang C. C., Huang L. W., Chang M. H., Lee I. H., et al. (2011). The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan. PLoS ONE 6:e29393. 10.1371/journal.pone.0029393 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Luigetti M., Fabrizi G. M., Madia F., Ferrarini M., Conte A., Del Grande A., et al. (2010). A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype. J. Neurol. Sci. 298, 114–117. 10.1016/j.jns.2010.09.008 [DOI] [PubMed] [Google Scholar]
- Lupo V., Garcia-Garcia F., Sancho P., Tello C., Garcia-Romero M., Villarreal L., et al. (2016). Assessment of Targeted Next-Generation Sequencing as a Tool for the Diagnosis of Charcot-Marie-Tooth Disease and Hereditary Motor Neuropathy. J. Mol. Diagn. 18, 225–234. 10.1016/j.jmoldx.2015.10.005 [DOI] [PubMed] [Google Scholar]
- Macario A. J., Conway de Macario E. (2007). Chaperonopathies and chaperonotherapy. FEBS Lett. 581, 3681–3688. 10.1016/j.febslet.2007.04.030 [DOI] [PubMed] [Google Scholar]
- Maeda K., Idehara R., Hashiguchi A., Takashima H. (2014). A family with distal hereditary motor neuropathy and a K141Q mutation of small heat shock protein HSPB1. Intern. Med. 53, 1655–1658. 10.2169/internalmedicine.53.2843 [DOI] [PubMed] [Google Scholar]
- Mandich P., Grandis M., Varese A., Geroldi A., Acquaviva M., Ciotti P., et al. (2010). Severe neuropathy after diphtheria-tetanus-pertussis vaccination in a child carrying a novel frame-shift mutation in the small heat-shock protein 27 gene. J. Child Neurol. 25, 107–109. 10.1177/0883073809334387 [DOI] [PubMed] [Google Scholar]
- Manganelli F., Tozza S., Pisciotta C., Bellone E., Iodice R., Nolano M., et al. (2014). Charcot-Marie-Tooth disease: frequency of genetic subtypes in a Southern Italy population. J. Peripher. Nerv. Syst. 19, 292–298. 10.1111/jns.12092 [DOI] [PubMed] [Google Scholar]
- Muranova L. K., Weeks S. D., Strelkov S. V., Gusev N. B. (2015). Characterization of Mutants of Human Small Heat Shock Protein HspB1 Carrying Replacements in the N-Terminal Domain and Associated with Hereditary Motor Neuron Diseases. PLoS ONE 10:e0126248. 10.1371/journal.pone.0126248 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Murphy S. M., Laura M., Fawcett K., Pandraud A., Liu Y. T., Davidson G. L., et al. (2012). Charcot-Marie-Tooth disease: frequency of genetic subtypes and guidelines for genetic testing. J. Neurol. Neurosurg. Psychiatr. 83, 706–710. 10.1136/jnnp-2012-302451 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nakhro K., Park J. M., Kim Y. J., Yoon B. R., Yoo J. H., Koo H., et al. (2013). A novel Lys141Thr mutation in small heat shock protein 22 (HSPB8) gene in Charcot-Marie-Tooth disease type 2L. Neuromuscul. Disord. 23, 656–663. 10.1016/j.nmd.2013.05.009 [DOI] [PubMed] [Google Scholar]
- Nefedova V. V., Datskevich P. N., Sudnitsyna M. V., Strelkov S. V., Gusev N. B. (2013). Physico-chemical properties of R140G and K141Q mutants of human small heat shock protein HspB1 associated with hereditary peripheral neuropathies. Biochimie 95, 1582–1592. 10.1016/j.biochi.2013.04.014 [DOI] [PubMed] [Google Scholar]
- Nefedova V. V., Muranova L. K., Sudnitsyna M. V., Ryzhavskaya A. S., Gusev N. B. (2015). Small heat shock proteins and distal hereditary neuropathies. Biochem. Mosc. 80, 1734–1747. 10.1134/S000629791513009X [DOI] [PubMed] [Google Scholar]
- Oberstadt M., Mitter D., Classen J., Baum P. (2016). Late onset dHMN II caused by c.404C>G mutation in HSPB1 gene. J. Peripher. Nerv. Syst. 21, 111–113. 10.1111/jns.12165 [DOI] [PubMed] [Google Scholar]
- Rossor A. M., Davidson G. L., Blake J., Polke J. M., Murphy S. M., Houlden H., et al. (2012b). A novel p.Gln175X [corrected] premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2. J. Peripher. Nerv. Syst. 17, 201–205. 10.1111/j.1529-8027.2012.00400.x [DOI] [PubMed] [Google Scholar]
- Rossor A. M., Kalmar B., Greensmith L., Reilly M. M. (2012a). The distal hereditary motor neuropathies. J. Neurol. Neurosurg. Psychiatr. 83, 6–14. 10.1136/jnnp-2011-300952 [DOI] [PubMed] [Google Scholar]
- Rusmini P., Polanco M. J., Cristofani R., Cicardi M. E., Meroni M., Galbiati M., et al. (2015). Aberrant autophagic response in the muscle of a knock-in mouse model of spinal and bulbar muscular atrophy. Sci. Rep. 5:15174. 10.1038/srep15174 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sanchez E., Darvish H., Mesias R., Taghavi S., Firouzabadi S. G., Walker R. H., et al. (2016). Identification of a large DNAJB2 deletion in a family with spinal muscular atrophy and parkinsonism. Hum. Mutat. 37, 1180–1189. 10.1002/humu.23055 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scarlato M., Vigano F., Carrera P., Previtali S. C., Bolino A. (2015). A novel heat shock protein 27 homozygous mutation: widening of the continuum between MND/dHMN/CMT2. J. Peripher. Nerv. Syst. 20, 419–421. 10.1111/jns.12139 [DOI] [PubMed] [Google Scholar]
- Shemetov A. A., Seit-Nebi A. S., Gusev N. B. (2008). Structure, properties, and functions of the human small heat-shock protein HSP22 (HspB8, H11, E2IG1): a critical review. J. Neurosci. Res. 86, 264–269. 10.1002/jnr.21441 [DOI] [PubMed] [Google Scholar]
- Sivera R., Sevilla T., Vilchez J. J., Martinez-Rubio D., Chumillas M. J., Vazquez J. F., et al. (2013). Charcot-Marie-Tooth disease: genetic and clinical spectrum in a Spanish clinical series. Neurology 81, 1617–1625. 10.1212/WNL.0b013e3182a9f56a [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith H. L., Li W., Cheetham M. E. (2015). Molecular chaperones and neuronal proteostasis. Semin. Cell Dev. Biol. 40, 142–152. 10.1016/j.semcdb.2015.03.003 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Solla P., Vannelli A., Bolino A., Marrosu G., Coviello S., Murru M. R., et al. (2010). Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charcot-Marie-Tooth and distal hereditary motor neuropathy. J. Neurol. Neurosurg. Psychiatr. 81, 958–962. 10.1136/jnnp.2009.181636 [DOI] [PubMed] [Google Scholar]
- Stancanelli C., Fabrizi G. M., Ferrarini M., Cavallaro T., Taioli F., Di Leo R., et al. (2015). Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family. Neurol. Sci. 36, 1003–1006. 10.1007/s10072-014-2050-8 [DOI] [PubMed] [Google Scholar]
- Sugiyama Y., Suzuki A., Kishikawa M., Akutsu R., Hirose T., Waye M. M., et al. (2000). Muscle develops a specific form of small heat shock protein complex composed of MKBP/HSPB2 and HSPB3 during myogenic differentiation. J. Biol. Chem. 275, 1095–1104. 10.1074/jbc.275.2.1095 [DOI] [PubMed] [Google Scholar]
- Sun Y., MacRae T. H. (2005). The small heat shock proteins and their role in human disease. FEBS J. 272, 2613–2627. 10.1111/j.1742-4658.2005.04708.x [DOI] [PubMed] [Google Scholar]
- Tang B., Liu X., Zhao G., Luo W., Xia K., Pan Q., et al. (2005). Mutation analysis of the small heat shock protein 27 gene in Chinese patients with Charcot-Marie-Tooth disease. Arch. Neurol. 62, 1201–1207. 10.1001/archneur.62.8.1201 [DOI] [PubMed] [Google Scholar]
- Tang B. S., Zhao G. H., Luo W., Xia K., Cai F., Pan Q., et al. (2005). Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L. Hum. Genet. 116, 222–224. 10.1007/s00439-004-1218-3 [DOI] [PubMed] [Google Scholar]
- Teive H. A. G., Arruda W. O., Scola R. H., Werneck L. C., Kok F. (2015). Distal neuropathy motor neuropathy with HSJ1 chaperone mutation, presenting with peripheral motor neuropathy, associated to Parkinsonism, and cerebellar ataxia: Case Report. Parkinsonism Relat. Disord. 22:e154 10.1016/j.parkreldis.2015.10.361 [DOI] [Google Scholar]
- Vicario M., Skaper S. D., Negro A. (2014). The small heat shock protein HspB8: role in nervous system physiology and pathology. CNS Neurol. Disord. Drug Targets 13, 885–895. 10.2174/1871527313666140711093344 [DOI] [PubMed] [Google Scholar]
- Walker L. C., Levine H., III., Mattson M. P., Jucker M. (2006). Inducible proteopathies. Trends Neurosci. 29, 438–443. 10.1016/j.tins.2006.06.010 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yavarna T., Al-Dewik N., Al-Mureikhi M., Ali R., Al-Mesaifri F., Mahmoud L., et al. (2015). High diagnostic yield of clinical exome sequencing in Middle Eastern patients with Mendelian disorders. Hum. Genet. 134, 967–980. 10.1007/s00439-015-1575-0 [DOI] [PubMed] [Google Scholar]
- Ylikallio E., Johari M., Konovalova S., Moilanen J. S., Kiuru-Enari S., Auranen M., et al. (2014). Targeted next-generation sequencing reveals further genetic heterogeneity in axonal Charcot-Marie-Tooth neuropathy and a mutation in HSPB1. Eur. J. Hum. Genet. 22, 522–527. 10.1038/ejhg.2013.190 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ylikallio E., Konovalova S., Dhungana Y., Hilander T., Junna N., Partanen J. V., et al. (2015). Truncated HSPB1 causes axonal neuropathy and impairs tolerance to unfolded protein stress. BBA Clin 3, 233–242. 10.1016/j.bbacli.2015.03.002 [DOI] [PMC free article] [PubMed] [Google Scholar]
- Zhai J., Lin H., Julien J. P., Schlaepfer W. W. (2007). Disruption of neurofilament network with aggregation of light neurofilament protein: a common pathway leading to motor neuron degeneration due to Charcot-Marie-Tooth disease-linked mutations in NFL and HSPB1. Hum. Mol. Genet. 16, 3103–3116. 10.1093/hmg/ddm272 [DOI] [PubMed] [Google Scholar]