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一种具有局限于肾脏分布的独特IV型胶原α链的鉴定及其基因定位于X染色体连锁的奥尔波特综合征位点。

Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome.

作者信息

Hostikka S L, Eddy R L, Byers M G, Höyhtyä M, Shows T B, Tryggvason K

机构信息

Biocenter, University of Oulu, Finland.

出版信息

Proc Natl Acad Sci U S A. 1990 Feb;87(4):1606-10. doi: 10.1073/pnas.87.4.1606.

Abstract

We have identified and extensively characterized a type IV collagen alpha chain, referred to as alpha 5(IV). Four overlapping cDNA clones isolated contain an open reading frame for 543 amino acid residues of the carboxyl-terminal end of a collagenous domain, a 229-residue carboxyl-terminal noncollagenous domain, and 1201 base pairs coding for a 3' untranslated region. The collagenous Gly-Xaa-Yaa repeat sequence has five imperfections that coincide with those in the corresponding region of the alpha 1(IV) chain. The noncollagenous domain has 12 conserved cysteine residues and 83% and 63% sequence identity with the noncollagenous domains of the alpha 1(IV) and alpha 2(IV) chains, respectively. The alpha 5(IV) chain has less sequence identity with the putative bovine alpha 3(IV) and alpha 4(IV) chains. Antiserum against an alpha 5(IV) synthetic peptide stained a polypeptide chain of about 185 kDa by immunoblot analysis and immunolocalization of the chain in human kidney was almost completely restricted to the glomerulus. The gene was assigned to the Xq22 locus by somatic cell hybrids and in situ hybridization. This may be identical or close to the locus of the X chromosome-linked Alport syndrome that is believed to be a type IV collagen disease.

摘要

我们已经鉴定并广泛表征了一种IV型胶原α链,称为α5(IV)。分离出的四个重叠cDNA克隆包含一个开放阅读框,其编码一个胶原结构域羧基末端543个氨基酸残基、一个229个残基的羧基末端非胶原结构域以及编码3'非翻译区的1201个碱基对。胶原Gly-Xaa-Yaa重复序列有五个缺陷,与α1(IV)链相应区域的缺陷一致。非胶原结构域有12个保守的半胱氨酸残基,与α1(IV)链和α2(IV)链的非胶原结构域的序列同一性分别为83%和63%。α5(IV)链与推测的牛α3(IV)和α4(IV)链的序列同一性较低。通过免疫印迹分析,抗α5(IV)合成肽的抗血清对一条约185 kDa的多肽链进行了染色,并且该链在人肾中的免疫定位几乎完全局限于肾小球。通过体细胞杂种和原位杂交将该基因定位于Xq22位点。这可能与X染色体连锁的Alport综合征的位点相同或接近,Alport综合征被认为是一种IV型胶原疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9815/53524/8240adf21122/pnas01029-0359-a.jpg

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