| Literature DB >> 25152455 |
Gen Tamiya1, Satoshi Makino2, Makiko Hayashi3, Akiko Abe3, Chikahiko Numakura3, Masao Ueki2, Atsushi Tanaka4, Chizuru Ito5, Kiyotaka Toshimori5, Nobuhiro Ogawa6, Tomoya Terashima6, Hiroshi Maegawa6, Daijiro Yanagisawa7, Ikuo Tooyama7, Masayoshi Tada8, Osamu Onodera8, Kiyoshi Hayasaka9.
Abstract
Charcot-Marie-Tooth disease (CMT) is the most common inherited neuropathy characterized by clinical and genetic heterogeneity. Although more than 30 loci harboring CMT-causing mutations have been identified, many other genes still remain to be discovered for many affected individuals. For two consanguineous families with CMT (axonal and mixed phenotypes), a parametric linkage analysis using genome-wide SNP chip identified a 4.3 Mb region on 12q24 showing a maximum multipoint LOD score of 4.23. Subsequent whole-genome sequencing study in one of the probands, followed by mutation screening in the two families, revealed a disease-specific 5 bp deletion (c.247-10_247-6delCACTC) in a splicing element (pyrimidine tract) of intron 2 adjacent to the third exon of cytochrome c oxidase subunit VIa polypeptide 1 (COX6A1), which is a component of mitochondrial respiratory complex IV (cytochrome c oxidase [COX]), within the autozygous linkage region. Functional analysis showed that expression of COX6A1 in peripheral white blood cells from the affected individuals and COX activity in their EB-virus-transformed lymphoblastoid cell lines were significantly reduced. In addition, Cox6a1-null mice showed significantly reduced COX activity and neurogenic muscular atrophy leading to a difficulty in walking. Those data indicated that COX6A1 mutation causes the autosomal-recessive axonal or mixed CMT.Entities:
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Year: 2014 PMID: 25152455 PMCID: PMC4157141 DOI: 10.1016/j.ajhg.2014.07.013
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025