首页> 美国卫生研究院文献>The Journal of Biophysical and Biochemical Cytology >Uroplakin IIIb a urothelial differentiation marker dimerizes with uroplakin Ib as an early step of urothelial plaque assembly
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Uroplakin IIIb a urothelial differentiation marker dimerizes with uroplakin Ib as an early step of urothelial plaque assembly

机译:尿路上皮分化标记物Uroplakin IIIb与uroplakin Ib一起二聚化作为尿路上皮斑块组装的早期步骤

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摘要

Urothelial plaques consist of four major uroplakins (Ia, Ib, II, and III) that form two-dimensional crystals covering the apical surface of urothelium, and provide unique opportunities for studying membrane protein assembly. Here, we describe a novel 35-kD urothelial plaque-associated glycoprotein that is closely related to uroplakin III: they have a similar overall type 1 transmembrane topology; their amino acid sequences are 34% identical; they share an extracellular juxtamembrane stretch of 19 amino acids; their exit from the ER requires their forming a heterodimer with uroplakin Ib, but not with any other uroplakins; and UPIII-knockout leads to p35 up-regulation, possibly as a compensatory mechanism. Interestingly, p35 contains a stretch of 80 amino acid residues homologous to a hypothetical human DNA mismatch repair enzyme-related protein. Human p35 gene is mapped to chromosome 7q11.23 near the telomeric duplicated region of Williams-Beuren syndrome, a developmental disorder affecting multiple organs including the urinary tract. These results indicate that p35 (uroplakin IIIb) is a urothelial differentiation product structurally and functionally related to uroplakin III, and that p35–UPIb interaction in the ER is an important early step in urothelial plaque assembly.
机译:尿道斑由四种主要的尿道素(Ia,Ib,II和III)组成,它们形成覆盖尿道顶端表面的二维晶体,​​并为研究膜蛋白组装提供了独特的机会。在这里,我们描述了一种新型的35 kD尿路上皮斑相关糖蛋白,它与uroplakin III密切相关:它们具有相似的整体1型跨膜拓扑结构;它们的氨基酸序列具有34%相同性;它们共有19个氨基酸的细胞外近膜延伸;它们从ER退出时,需要与uroplakin Ib形成异源二聚体,而不与任何其他uroplakins形成异源二聚体。 UPIII敲除可能导致p35上调,可能是一种补偿机制。有趣的是,p35包含一段与假设的人类DNA错配修复酶相关蛋白同源的80个氨基酸残基。人类p35基因定位在Williams-Beuren综合征的端粒重复区域附近的染色体7q11.23,该疾病是一种影响包括尿路在内的多个器官的发育障碍。这些结果表明,p35(uroplakin IIIb)是与uroplakin III在结构和功能上相关的尿路上皮分化产物,而ER中的p35–UPIb相互作用是尿路上皮斑块组装的重要早期步骤。

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