首页> 外文期刊>Human Genetics >Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) families (published erratum appears in Hum Genet 2000 May;106(5):575)
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Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) families (published erratum appears in Hum Genet 2000 May;106(5):575)

机译:TRKA(NTRK1)基因编码的高亲和力神经生长因子受体的突变和多态性分析,该受体对先天性无汗症疼痛(CIPA)家族不敏感(发表的勘误表载于Hum Genet 2000 May; 106(5):575)

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摘要

The human TRKA gene encodes a high-affinity tyrosine kinase receptor for nerve growth factor. Congenital insensitivity to pain with anhidrosis (CIPA) is an autosomal recessive genetic disorder reported from various countries and characterized by anhidrosis (inability to sweat), the absence of reaction to noxious stimuli, and mental retardation. We have found that TRKA is the gene responsible for CIPA. We have studied TRKA in 46 CIPA chromosomes derived from 23 unrelated Japanese CIPA families. including three that have been previously reported, and identified 11 novel mutations. Four (L93P, G516R, R648 C, and D668Y) are missense mutations that result in amino acid substitutions at positions conserved in the TRK family, including TRKA, TRKB, and TRKC. Three (S131 fs, L579 fs, and D770 fs) are frameshift mutations. Three (E164X, Y359X, and R596X) are nonsense mutations. The other is an intronic branch-site (IVS7-33T-->A) mutation, causing aberrant splicing in vitro. We also report the characterization of eight intragenic polymorphic sites, including a variable dinucleotide repeat and seven single nucleotide polymorphisms, and describe the haplotypic associations of alleles at these sites in 106 normal chromosomes and 46 CIPA chromosomes. More than 50% of CIPA chromosomes share the frameshift mutation (R548 fs) that we described earlier. This mutation apparently shows linkage disequilibrium with a rare haplotype in normal chromosomes, strongly suggesting that it is a common founder mutation. These findings represent the first extensive analysis of CIPA mutations and associated intragenic polymorphisms; they should facilitate the detection of CIPA mutations and aid in the diagnosis and genetic counseling of this painless but severe genetic disorder with devastating complications.
机译:人TRKA基因编码神经生长因子的高亲和力酪氨酸激酶受体。先天性对患有脱水症的疼痛不敏感(CIPA)是世界上许多国家报告的常染色体隐性遗传疾病,其特征是脱水症(无汗),对有害刺激没有反应以及智力低下。我们发现TRKA是负责CIPA的基因。我们已经研究了来自23个无关的日本CIPA家族的46条CIPA染色体中的TRKA。包括之前已报道的三个突变,并鉴定出11个新突变。四个(L93P,G516R,R648 C和D668Y)是错义突变,可导致TRK家族保守位置(包括TRKA,TRKB和TRKC)的氨基酸取代。三个(S131 fs,L579 fs和D770 fs)是移码突变。三个(E164X,Y359X和R596X)是无意义的突变。另一个是内含子分支位点(IVS7-33T-> A)突变,在体外引起异常剪接。我们还报告了八个基因内多态性位点的表征,包括一个可变的双核苷酸重复和七个单核苷酸多态性,并描述了这些位点在106个正常染色体和46个CIPA染色体中的单倍型关联。超过50%的CIPA染色体共享我们先前描述的移码突变(R548 fs)。该突变显然显示出正常染色体中具有罕见单倍型的连锁不平衡,强烈表明这是一个常见的创始人突变。这些发现是对CIPA突变和相关的基因内多态性的首次广泛分析。他们应该促进CIPA突变的检测,并帮助诊断和遗传咨询这种无痛但严重的遗传性疾病,并具有破坏性的并发症。

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