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Isolation and chromosomal localization of cDNAs encoding a novel human lymphocyte cell surface molecule, LAM-1. Homology with the mouse lymphocyte homing receptor and other human adhesion proteins

机译:编码新型人类淋巴细胞表面分子LAM-1的cDNA的分离和染色体定位。与小鼠淋巴细胞归巢受体和其他人类黏附蛋白的同源性

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摘要

A cDNA encoding a new human lymphocyte cell surface molecule has been isolated and shown to identify a fourth member of a recently discovered family of adhesion proteins. This lymphocyte-associated molecule (LAM- 1) is uniquely composed of multiple distinct domains, one domain homologous with animal lectins, one homologous with epidermal growth factor, and two short consensus repeat units similar to those found in C3/C4 binding proteins. This cDNA clone hybridized with RNAs found in B cell lines and T lymphocytes, but not with RNA from other cell types. The amino acid sequence of LAM-1 is 77% homologous with the sequence of the mouse lymphocyte homing receptor, suggesting that LAM-1 may function in human lymphocyte adhesion. The LAM-1 gene is located on chromosome 1q23-25, as is another member of this adhesion family, suggesting that this new family of proteins may be encoded by a cluster of "adhesion protein" loci.
机译:已经分离出编码新的人类淋巴细胞表面分子的cDNA,并显示出它可以识别最近发现的粘附蛋白家族的第四个成员。该淋巴细胞相关分子(LAM-1)独特地由多个不同的域组成,一个域与动物凝集素同源,一个域与表皮生长因子同源,以及两个与C3 / C4结合蛋白相似的短共有重复单元。该cDNA克隆与B细胞系和T淋巴细胞中发现的RNA杂交,但不与其他细胞类型的RNA杂交。 LAM-1的氨基酸序列与小鼠淋巴细胞归巢受体的序列具有77%的同源性,这表明LAM-1可能在人淋巴细胞粘附中起作用。 LAM-1基因位于染色体1q23-25上,也是该粘附家族的另一个成员,这表明该新的蛋白质家族可能由“粘附蛋白”基因座簇编码。

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  • 年度 1989
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