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通过cDNA分离鉴定出一种新的IV型胶原链α6(IV),并将该基因定位于Xq22染色体,此位点与COL4A5相同。

Identification of a new collagen IV chain, alpha 6(IV), by cDNA isolation and assignment of the gene to chromosome Xq22, which is the same locus for COL4A5.

作者信息

Oohashi T, Sugimoto M, Mattei M G, Ninomiya Y

机构信息

Department of Molecular Biology and Biochemistry, Okayama University Medical School, Japan.

出版信息

J Biol Chem. 1994 Mar 11;269(10):7520-6.

PMID:8125972
Abstract

To date, five distinct alpha chains have been identified in basement membrane collagen IV. We have cloned a gene encoding a new alpha chain belonging to basement membrane collagen IV by cDNA isolation under low stringency conditions. Isolation of overlapping clones and the technique of 5' rapid amplification of cDNA ends enabled us to derive the primary structure of the entire polypeptide. The deduced collagen polypeptide contained 1678 amino acid residues, including a 21-residue signal peptide, a 24-residue amino-terminal NC domain, a central 1405-residue collagenous (COL1) domain, and a 228-residue carboxyl-terminal NC1 domain. We have designated this newly found alpha chain as the alpha 6(IV) chain. The gene was mapped to chromosome Xq22 by in situ hybridization of metaphase lymphocytes. This is the same region of chromosome X where the gene coding for the alpha 5(IV) collagen chain (COL4A5) resides. Mutations in COL4A5 have been characterized in more than 50 patients with Alport syndrome. However, some of the X-linked cases of Alport syndrome are not apparently caused by COL4A5 mutations. The gene we describe in this paper therefore seems to be a candidate for mutations in this group of Alport syndrome patients.

摘要

迄今为止,已在基底膜胶原蛋白IV中鉴定出五种不同的α链。我们通过在低严格条件下进行cDNA分离,克隆了一个编码属于基底膜胶原蛋白IV的新α链的基因。重叠克隆的分离以及5' cDNA末端快速扩增技术使我们能够推导整个多肽的一级结构。推导的胶原蛋白多肽包含1678个氨基酸残基,包括一个21个残基的信号肽、一个24个残基的氨基末端NC结构域、一个中央1405个残基的胶原(COL1)结构域和一个228个残基的羧基末端NC1结构域。我们将这个新发现的α链命名为α6(IV)链。通过中期淋巴细胞的原位杂交将该基因定位到X染色体q22区。这与编码α5(IV)胶原链(COL4A5)的基因所在的X染色体区域相同。超过50例Alport综合征患者的COL4A5突变已得到表征。然而,一些X连锁的Alport综合征病例显然不是由COL4A5突变引起的。因此,我们在本文中描述的基因似乎是这组Alport综合征患者突变的一个候选基因。

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