首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Chromosomal localization of the genes for the vitronectin and fibronectin receptors alpha subunits and for platelet glycoproteins IIb and IIIa.
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Chromosomal localization of the genes for the vitronectin and fibronectin receptors alpha subunits and for platelet glycoproteins IIb and IIIa.

机译: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的基因的染色体定位。

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摘要

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.
机译:整联蛋白是涉及细胞-细胞和细胞-基质相互作用的一系列相关膜受体,是α和β亚基的异二聚体复合物。为了开始理解这些复合物的进化,我们研究了几个α和β整联蛋白亚基的基因组组织。使用体细胞杂种和原位杂交技术,我们已经确定了玻连蛋白受体(VNR alpha),纤连蛋白受体(FNR alpha)和血小板α亚基的α基因的染色体位置糖蛋白IIb / IIIa复合物,GPIIb。此外,我们已经确定了GPIIb / IIIa异二聚体GPIIIa的β亚基基因的染色体位置。我们的研究表明,α亚基并不局限于单个基因座,而是每个亚基都位于不同的染色体上。 VNR alpha的基因位于2号染色体,FNR alpha的基因位于12q11 ---- 13染色体,GPIIb的基因位于17q21 ---- 23染色体。与α亚基的染色体分散相反,GPIIb和GPIIIa的基因在物理上接近,而GPIIIa的基因也位于染色体17q21 ---- 23上。这些研究表明,整合蛋白家族的α亚基的基因在进化过程中已经分散,而GPIIb和GPIIIa在物理上紧密接近。 GPIIb和GPIIIa的这种物理接近性可能参与巨核细胞同时表达这些蛋白质,并可能导致这两个基因之间的连锁不平衡,这将限制在小规模GPIIb / IIIa异常的连锁研究中使用限制性长度多态性。亲戚。

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