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基底膜胶原蛋白IV基因的组织与表达及其在人类疾病中的作用。

Organization and expression of basement membrane collagen IV genes and their roles in human disorders.

作者信息

Sado Y, Kagawa M, Naito I, Ueki Y, Seki T, Momota R, Oohashi T, Ninomiya Y

机构信息

Division of Immunology Okayama University Medical School, 2-5-1 Shikata-cho, Okayama 700-8558, USA.

出版信息

J Biochem. 1998 May;123(5):767-76. doi: 10.1093/oxfordjournals.jbchem.a022003.

DOI:10.1093/oxfordjournals.jbchem.a022003
PMID:9562604
Abstract

Six distinct genes have been identified as belonging to the type IV collagen gene family. They can be organized into three sets, i.e., COL4A1/COL4A2, COL4A3/COL4A4, and COL4A5/COL4A6, which are localized on three different chromosomes in humans, 13, 2, and X, respectively. Within each set the genes are aligned head-to-head and their expression is regulated by bidirectional promoters between the genes. Transcriptional regulation of the COL4A1/COL4A2 set has been well characterized. The transcription of COL4A6 seems to be controlled by two alternative promoters. While collagen IV molecules composed of alpha1 and alpha2 chains are broadly distributed, molecules comprising combinations of the other four chains, alpha3-alpha6, are important components of specialized basement membranes. The precise chain composition of triple-helical molecules assembled from the alpha3-alpha6 chains is not entirely clear, but it is hypothesized that alpha3-alpha5 chains and alpha5 and alpha6 chains form heterotrimeric molecules. Several pieces of evidence indicate that alpha3/alpha4/alpha5 molecules and alpha5/alpha6 molecules are components of the basement membrane network. This helps explain the observation that the kidney and skin basement membranes from patients with Alport syndrome caused by mutations in the alpha5 coding gene, COL4A5, are defective in the alpha3, alpha4, and alpha6 chains together with the alpha5 chain. Large deletions involving the COL4A5 and COL4A6 genes have been found in rare cases of diffuse leiomyomatosis associated with Alport syndrome.

摘要

六个不同的基因已被确定属于IV型胶原基因家族。它们可分为三组,即COL4A1/COL4A2、COL4A3/COL4A4和COL4A5/COL4A6,分别定位于人类的三条不同染色体上,即13号、2号和X染色体。在每组基因中,基因是头对头排列的,它们的表达受基因之间的双向启动子调控。COL4A1/COL4A2组的转录调控已得到充分表征。COL4A6的转录似乎受两个替代启动子控制。虽然由α1和α2链组成的IV型胶原分子广泛分布,但由其他四条链α3-α6组合而成的分子是特殊基底膜的重要组成部分。由α3-α6链组装而成的三螺旋分子的确切链组成尚不完全清楚,但据推测α3-α5链以及α5和α6链形成异源三聚体分子。几条证据表明α3/α4/α5分子和α5/α6分子是基底膜网络的组成部分。这有助于解释以下观察结果:由α5编码基因COL4A5突变导致的Alport综合征患者的肾和皮肤基底膜在α3、α4和α6链以及α5链上存在缺陷。在与Alport综合征相关的罕见弥漫性平滑肌瘤病病例中发现了涉及COL4A5和COL4A6基因的大片段缺失。

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