The peripheral myelin protein 22 (PMP22) gene is located within the duplication region. Several lines of evidence implicate alterations in gene dosage of PMP22 as the main factor underlying the CMT1A phenotype.14,15 This means that patients carrying one extra copy of PMP22 develop CMT1A, while patients with HNPP (hereditary neuropathy with liability to pressure palsies) deletion have only one copy of PMP22 (Fig. 2).

The early growth response 2 (EGR2) gene encodes a zinc finger transcription factor that plays a major role in myelination of peripheral nerves.32 EGR2 mutations are associated with a dominantly inherited severe form of CMT1, giving syndromes of congenital hypomyelination (CH), DSS, or CMT4E with recessive inheritance.33 Disruption of the EGR2 gene in mice blocks the development of Schwann cells at the promyelinating stage and causes demyelinating peripheral neuropathy by preventing PNS myelination.34 Thus, the normal expression of the EGR2 gene is very important in the process of Schwann cell development.34 In a recent study, overexpression of EGR2 in Schwann cells strongly increased the expression of other myelin-related genes; therefore, EGR2 mutation may cause a demyelinating form of CMT.35

A CMT family with two missense mutations in different genes has been reported.36 A R359W mutation in EGR2 was shared by the affected daughter and her father. In addition, she had a V136A mutation in GJB1, which was determined to be a de novo mutation. The daughter with two different gene mutations showed more severe clinical, electrophysiological, and histopathological phenotypes than her father, who had only the EGR2 mutation. These phenotypic differences between the proband and her father may have been caused by an altered effect of the genetic modifier in EGR2, or by the additive effect of the EGR2 and GJB1 mutations.36

The EGR2 gene regulates the expressions of myelin genes, including GJB1, PMP22, P0, and PRX in a dominant-negative manner.37,38 Mutations in EGR2 prevent Schwann cell development, and lead to the development of demyelinating neuropathy via the regulation of GJB1 expression (Fig. 3).37 Moreover, it is known that the R359W mutation in EGR2 reduces transcriptional activity in GJB1.38

Mutations in the LITAF (lipopolysaccharide-induced tumor necrosis factor-alpha factor, also referred to as SIMPLE) gene cause the demyelinating autosomal dominant disease CMT1C.9 Patients with CMT1C have decreased NCVs of 20~25 m/s, along with mild weakness and sensory loss that first presents within the first two decades of life.39 They show very similar clinical findings to CMT1A. SIMPLE is a protein encoded by the LITAF gene and may interact with Nedd4, an E3 ubiquiton ligase.40 Although SIMPLE is expressed in many cell types, when mutated it seems to cause only a demyelinating neuropathy. The disease specificity may result from the impaired degeneration of specific Shwann cell proteins.40

CMT4F is a severe from of recessive CMT that has been defined in a large Lebanese family with mutations in the periaxin (PRX) gene on chromosome 19.41 Nerve conduction is markedly slowed and onion bulbs are observed on sural nerve biopsies. PRX is a protein specifically expressed by myelinating Schwann cells.42 In adult myelinated fibers, PRX is found in the abaxonal membrane.38 During development, PRX is found in the adaxonal membrane or periaxonal cytoplasm of the myelinating Schwann cell and may have some additional function.43,44 Furthermore, an isoform of PRX is targeted to the nucleus of embryonic Schwann cells, suggesting that this protein can shuttle between the nucleus and cortical signaling or adherence complexes. Histopathological analysis of a nerve biopsy from a CMT4F patient revealed disruption of the connection between the paranodal loop and the adjacent axon; structural abnormality of the paranode was also present.45

Mutations in the gene encoding myotubularin-related phosphatase 2 (MTMR2) cause a severe autosomalrecessive, demyelinating neuropathy, CMT4B1, which has also been called hereditary motor and sensory neuropathy with focally folded myelin sheaths.46 MTMR2 contains a homologous 10-amino acid sequence with an active site for both tyrosine and serine phosphate.47 The function of MTMR2 is not yet known. However, teased fibers from sural nerve biopsy samples showed segmental demyelination associated with redundant loops of myelin, suggesting that MTMR2 has an important role in the regulation of myelin wrapping.48

Mutations in MTMR13/SBF2 have been identified in severe autosomal recessive demyelinating CMT, CMT4B2.49 SBF2 is located on chromosome 11p15 and is also known as myotubulin-related protein 13 (MTMR13). MTMR13/SBF2 is a homologue of MTMR2, which causes CMT4B1.49 This is probably the reason for CMT4B2 neuropathy resembling that of CMT4B1 both clinically and pathologically. These peripheral neuropathies show very severe disabilities in infancy and extremely slow NCVs. Sometimes patients are wheelchairbound by adulthood. Because the pathological findings of CMT4B1 and CMT4B2 are found simultaneously with the misfoldings of myelin, they probably share a common pathological mechanism. SBF2 might regulate phosphatase activity by interacting with MTMR2.9

By linkage analysis and screening genes linked to the CMT2A locus, Züchner et al. first identified several mutations in the mitofusion 2 (MFN2) gene.50 Subsequently, additional MFN2 mutations were reported in CMT2A patients (Fig. 4).51,52 Thus, mutations in MFN2 are now considered to provide the genetic basis of the CMT2A phenotype. Mitofusin 2 encodes an outer mitochondrial membrane protein which, in cooperation with the MFN1 isoform, has important roles in the regulation of mitochondrial fusion,53-55 a function essential for metabolic activity in eukaryotic cells.56 It has also been suggested that MFN2 may be associated with maintaining mitochondrial membrane potentials.57 Moreover, MFN2-deficient mice die in mid-gestation and display fragmented mitochondria.54 It is also believed, from a few population-based studies, that MFN2 mutations are most common in CMT2.58 Recently, axonal CMT neuropathy with visual impairment due to optic atrophy - designated as hereditary motor and sensory neuropathy type VI (HMSN VI) - has also been shown to be caused by mutations in the MFN2 gene.59 It is well known that HMSN VI is an axonal CMT neuropathy with optic atrophy. However, the differences between CMT2A and HMSN VI with MFN2 mutations remain to be clarified. It appears that mutational loci with high frequency might exist in MFN2 at the 94th, 105th, 280th, and 364th codons.60

Ethnic population data on MFN2 mutations are limited because the relevance of the MFN2 mutation to CMT2 has been reported only recently.50 Zuchner et al. reported 7 mutations (19%) in 36 CMT2 families representing several ethnic groups; a Japanese group reported 7 mutations (9%) in 81 axonal or unclassified CMT patients,47 and an American study found 3 mutations (23%) in 13 CMT2 families.50-52 In addition, MFN2 mutations have been identified in 22% of Korean CMT2 families.60 The mutation frequency observed by the Japanese group was lower than that found in the other studies, which may be due to sampling or analytical differences or perhaps to different genetic backgrounds. Kijima et al. performed denaturing high-performance liquid chromatography (HPLC) prior to sequence analysis, a process that may have reduced the detection rate.51

Mutations in the MFN2 gene are now viewed as the primary cause of axonal autosomal-dominant CMT2A, and it has therefore been suggested that these patients should be screened for MFN2. However, clinical and electrophysiological phenotypes of CMT patients with MFN2 mutations were significantly different in earlyand late-onset groups, and optic atrophy was found only in CMT2 patients with unusually severe phenotypes with an early onset age. In addition, MFN2 mutations show variable central nervous system (CNS) involvements.

Following the mapping of CMT2A to the short arm of chromosome 1, 1p35-p36, a missense mutation was detected in KIF1B in a Japanese CMT2A family.61 However, no other mutation has been identified in KIF1B, and it is therefore believed that another gene is involved.62,63 The kinesin superfamily is responsible for microtubule-dependent transport of a variety of organelles and vesicles.

It has been reported that mutations in the ras-related protein rab-7 (RAB7) gene cause the axonal form of CMT known as CMT2B.64 RAB7 is a member of the Rab family of small G proteins, which regulate intracellular vesicle traffic. RAB7 and its effector protein, RILP, have been shown to play a role in lysosomal transport by inducing the recruitment of dynein-dynactin motors.65 Mutations in dynactin also cause axonopathy, suggesting that two separate diseases may share a common pathway.

Mutations of the small heat-shock proteins (sHSPs) are reported to cause either CMT2 or a distal hereditary motor neuropathy (dHMN).66 It is known that sHSPs are part of a protein superfamily sharing 85 amino acid residues in a C-terminal region known as the α-crystalline domain, although the function of sHSP is unclear. However, it is believed that sHSP27 is associated with protection from apoptosis and stabilization of the cytoskeleton.67 Irobi et al.66 reported that mutations in the α-crystalline domain of sHSP22 cause dHMN type II; Evgrafov et al.68 suggested that mutations in the α-crystalline and C-terminal tail of sHSP27 cause either CMT2F or another dHMN. It seems that sHSP22 and sHSP27 interact with each other, and both diseases involve common mechanisms.69,70

Glycyl-tRNA synthetase is known to cause CMT2D.71 In four families with CMT2D, mutation of Glycyl-tRNA synthetase provided the first example of an aminoacyl tRNA synthetase which was related to human genetic disease.71 Why a mutation in a tRNA synthetase should cause only a chronic neuropathy but spare other organ systems is both unknown and surprising.

Mutations in the myelin protein zero (MPZ) gene, which is located on chromosome 1q21-q22, are present in CMT1B, CMT type 2, DSS, and CH neuropathy.72,73 It is proposed that the nature and position of the MPZ mutations largely determine the axonal and demyelinating phenotypes. MPZ is highly expressed by myelinating Schwann cells and in more than half the protein in the peripheral myelin sheet. The clinical, electrophysiological, and histopathological findings appear to be heterogeneous for MPZ mutations.74 Furthermore, the same mutation can cause different degrees of disease severity in different patients.75

The protein consists of 248 amino acids and a single extracellular immunoglobulin-related domain (which mediates homophilic adhesion), a transmembrane domain, and a short basic intracellular domain.76 MPZ knock-out mice show abnormal regulation of myelin gene expression such as upregulation of MAG and PLP and downregulation of PMP22.77 The myelination regulatory mechanism of MPZ is through adhesion-mediated signal transduction.78 By this hypothesis, the in vitro mutations of MPZ are associated with decreased MPZ-mediated adhesion and these changes cause the more severe clinical features.

Neurofilament light-chain polypeptide (NEFL) is one of the most abundant cytoskeletal components of the neuron.79 The NEFL gene encoding the neurofilament plays an important role in axonal structure, including that of the extensive fibrous network in the cytoplasm of the neuron (Fig. 5).79 Mutations in the NEFL gene usually cause axonal CMT2E neuropathy, but recent studies found that NEFL mutations cause the demyelinating forms of neuropathy common to CMT1 and DSS.80

Nerve conduction studies of CMT2E patients showed that NCV is not decreased severely. These findings suggest that the pathophysiological mechanism of the neuropathy is primary axonal damage.81 A patient with NEFL gene mutation shows proximal muscle weakness, normal NCV, and reduced motor and sensory nerve action potential amplitudes, findings compatible with typical CMT2. Transgenic mice harboring loss of NEFL genes show a normal phenotype; however, NCVs are severely reduced.82,83 Mutation of the NEFL gene could be the cause of both CMT1 and CMT2 neuropathies. Population data on the mutation frequencies of the NEFL gene are very limited. The frequencies of NEFL were 4.8% in Koreans and 2.2% in Caucasian CMT patients.84,85

CMTX is the second-most-frequent form of CMT, and is caused by mutations in the gene for gap junction protein beta 1 (GJB1: connexin 32, Cx32), which maps to chromosome Xq13.86,87 CMTX patients display the distinctive criterion of an X-linked mode of inheritance; that is, an absence of man-to-man transmission and a more severe disease phenotype in affected males than in affected females of the same age.88 Motor nerve conduction is slower in CMTX males, but ranges from slightly reduced to normal in females.89 The nature of the neuropathy in CMTX remains controversial, and it could be a primary axonal neuropathy or a primary demyelinating neuropathy with secondary axonal degeneration.90,91

The GJB1 gene is involved in the transport of small molecules within Schwann cells.92 Gap junctions allow electrical communication between cells in the nervous system and GJB1 mutations affect the function of gap junctions in the myelin sheath.93 Gap junctions comprise intercellular channels among adjacent cells and they are distributed in the liver, kidneys, and CNS as well as the peripheral nerves.94 Since the GJB1 gene is expressed not only in Schwann cells but also in oligodendrocytes, GJB1 mutation has been reported to cause CNS lesions.95 There are over 200 mutations associated with various degrees of muscular weakness, atrophy, and sensory impairment. In studies of CMTX patients, mutation of GJB1 more or less destroyed the structure of the myelin and the action potential amplitude was more affected than the NCV.96 Sural nerve biopsy confirmed that there was prominent axonal loss.97

The mutation frequency of GJB1 in Korea (7.1%)85 is considerably lower than in several European groups - Spain, 21.3%98; Finland, 19.0%99; Russia, 13.0%100; Italy, 16.7%101; Germany, 11.9%102 - but is similar to that in Japan (5.6~5.7%).103,104 It appears that mutations in GJB1 are less frequent in East Asian CMT patients than in European patients.

CMT4A is linked to 8q13-q21.1 and is caused by mutations in ganglioside-induced differentiated associated protein 1 (GDAP1), a novel protein of unknown function. 105 Clinical symptoms begin at an early age (before 10 years), with delayed developmental milestones of sitting or walking; weakness spreads to proximal muscles by the end of the first decade. However, sensory loss is mild. In other patients, hoarse voice and vocal cord paresis have been reported. Axonal and demyelinating phenotypes have been associated with GDAP1 mutations, which could be the cause of both the demyelinating and axonal neuropathies.106 The GDAP1 gene is found in the nerve cell at an early stage of development but its expression is found in the Schwann cell.107 It is not yet known if mutation of the GDAP1 gene damages the nerve cell, Schwann cell, or both. However, a likely hypothesis is that mutation of the GDAP1 gene disturbs signal transmission between Schwann cells and nerve cells.

Mutations in the Gigaxonin gene lead to a rare autosomal-recessive giant axonal neuropathy (GAN) affecting the peripheral nervous system and CNS.108 Prominent axonal swelling occurs, with masses of tightly woven neurofilaments - commonly found near nodes of Ranvier - producing an increase in axon caliber.109 This causes the main stigmata of the disease. Abnormalities in the organization of neurofilaments are also found in the brains of these patients, and are the possible cause of the associated mental retardation.

GAN includes abnormal intermediate neurofilaments and displays the typically kinky-hair-like filaments. The mechanism of the disease is unknown, but the peripheral neuropathy is developed by the mutation of the Gigaxonin gene, which possibly induces changes in the axon transport system and a resulting deficiency in energy.

CMT4C is caused by homozygous or compound heterozygous mutations in the previously uncharacterized KIAA1985 gene.110 CMT4C is a childhood-onset disease associated with an early-onset scoliosis and a distinct Shwann cell pathology. Scoliosis is prominent early on and may precede weakness and sensory loss. The protein encoded by KIAA1985 belongs to new vertebrate protein group whose function is not known. By means of comparative sequence alignment, it is possible to determine that this protein group includes the multiple SH3 and TRP domains which are associated with formation of protein polymers.110