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玻连蛋白和纤连蛋白受体α亚基以及血小板糖蛋白IIb和IIIa基因的染色体定位。

Chromosomal localization of the genes for the vitronectin and fibronectin receptors alpha subunits and for platelet glycoproteins IIb and IIIa.

作者信息

Sosnoski D M, Emanuel B S, Hawkins A L, van Tuinen P, Ledbetter D H, Nussbaum R L, Kaos F T, Schwartz E, Phillips D, Bennett J S

机构信息

Howard Hughes Medical Institute, University of Pennsylvania School of Medicine, Philadelphia 19104.

出版信息

J Clin Invest. 1988 Jun;81(6):1993-8. doi: 10.1172/JCI113548.

Abstract

The integrins, a family of related membrane receptors involved in cell-cell and cell-matrix interactions, are heterodimeric complexes of alpha and beta subunits. To begin to understand the evolution of these complexes, we studied the genomic organization of several alpha and beta integrin subunits. Using both somatic cell hybrids and an in situ hybridization technique, we have determined the chromosomal location of the genes for the alpha subunits of the vitronectin receptor (VNR alpha), the fibronectin receptor (FNR alpha), and for the alpha subunit of the platelet glycoprotein IIb/IIIa complex, GPIIb. In addition, we have determined the chromosomal location of the gene for the beta subunit of the GPIIb/IIIa heterodimer, GPIIIa. Our studies indicate that the alpha subunits do not localize to a single locus, but that each is found on a different chromosome. The gene for VNR alpha is located on chromosome 2, the gene for FNR alpha is on chromosome 12q11----13, and the gene for GPIIb is on chromosome 17q21----23. In contrast to the chromosomal dispersion of the alpha subunits, the genes for GPIIb and GPIIIa are physically close, with the gene for GPIIIa also located on chromosome 17q21----23. These studies indicate that the genes for the alpha subunits of the integrin family have been dispersed during evolution while GPIIb and GPIIIa are in close physical proximity. This physical proximity of GPIIb and GPIIIa may be involved in the concurrent expression of these proteins by megakaryocytes, and may result in linkage disequilibrium between these two genes, which would limit the use of restriction length polymorphisms in linkage studies of GPIIb/IIIa abnormalities in small kindreds.

摘要

整合素是一族参与细胞间和细胞与基质相互作用的相关膜受体,为α和β亚基组成的异二聚体复合物。为了初步了解这些复合物的进化过程,我们研究了几种α和β整合素亚基的基因组结构。利用体细胞杂交和原位杂交技术,我们确定了玻连蛋白受体(VNRα)、纤连蛋白受体(FNRα)的α亚基以及血小板糖蛋白IIb/IIIa复合物(GPIIb)的α亚基基因的染色体定位。此外,我们还确定了GPIIb/IIIa异二聚体的β亚基(GPIIIa)基因的染色体定位。我们的研究表明,α亚基并不定位于单个位点,而是分布在不同的染色体上。VNRα基因位于第2号染色体上,FNRα基因位于第12号染色体的q11----13区域,GPIIb基因位于第17号染色体的q21----23区域。与α亚基的染色体分散情况不同,GPIIb和GPIIIa的基因在物理位置上很接近,GPIIIa基因也位于第17号染色体的q21----23区域。这些研究表明,整合素家族α亚基的基因在进化过程中已经分散,而GPIIb和GPIIIa在物理位置上紧密相邻。GPIIb和GPIIIa在物理位置上的这种紧密相邻可能与巨核细胞同时表达这些蛋白质有关,并且可能导致这两个基因之间的连锁不平衡,这将限制在小家系中对GPIIb/IIIa异常进行连锁研究时使用限制性片段长度多态性。

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