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编码α2-巨球蛋白受体相关蛋白的人类基因(LRPAP1)的克隆、特性分析及其在4p16上的染色体定位,以及与编码44 kDa肝素结合蛋白的鼠基因的结构比较。

Cloning, characterization, and chromosomal localization to 4p16 of the human gene (LRPAP1) coding for the alpha 2-macroglobulin receptor-associated protein and structural comparison with the murine gene coding for the 44-kDa heparin-binding protein.

作者信息

Van Leuven F, Hilliker C, Serneels L, Umans L, Overbergh L, De Strooper B, Fryns J P, Van den Berghe H

机构信息

Center for Human Genetics, University of Leuven, Belgium.

出版信息

Genomics. 1995 Jan 20;25(2):492-500. doi: 10.1016/0888-7543(95)80050-v.

Abstract

We report the molecular cloning of the human gene (symbol LRPAP1) coding for the alpha 2-macroglobulin receptor-associated protein (A2MRAP), as well as the gene coding for the 44-kDa heparin-binding protein (HBP-44), its murine counterpart. For both, genomic cosmid clones were isolated, and for the human gene a bacteriophage P1 clone containing the entire A2MRAP gene was also retrieved. The genes were characterized after subcloning: in both species, the known coding part of the cDNA is encoded by eight exons, and the position of the boundaries of the exons was conserved. The human LRPAP1 locus was assigned to chromosome 4 by PCR of human-hamster hybrid cell lines and by fluorescence in situ hybridization to band 4p16.3. This maps closely to the variable constitutional deletions of the short arm of chromosome 4, observed cytogenetically in patients with the Wolf-Hirschhorn syndrome. Metaphase spreads of two such patients were analyzed by fluorescence in situ hybridization with an LRPAP1 genomic probe. The first patient, with karyotype 46,XY,del4(p14-p16.1), had retained both copies of the LRPAP1 gene. In contrast, the other patient, with karyotype 46,XY,del4(p15.3-pter), displayed no signal for LRPAP1 on the deleted chromosome.

摘要

我们报道了编码α2-巨球蛋白受体相关蛋白(A2MRAP)的人类基因(符号为LRPAP1)以及编码44 kDa肝素结合蛋白(HBP - 44)及其小鼠对应物的基因的分子克隆。对于这两个基因,都分离出了基因组黏粒克隆,对于人类基因,还获得了一个包含整个A2MRAP基因的噬菌体P1克隆。在亚克隆后对这些基因进行了表征:在这两个物种中,cDNA的已知编码部分由八个外显子编码,并且外显子边界的位置是保守的。通过对人 - 仓鼠杂交细胞系进行PCR以及通过荧光原位杂交将人类LRPAP1基因座定位到染色体4的4p16.3带。这与在Wolf - Hirschhorn综合征患者中细胞遗传学观察到的4号染色体短臂的可变结构缺失紧密相关。用LRPAP1基因组探针通过荧光原位杂交分析了两名此类患者的中期染色体铺展。第一名患者核型为46,XY,del4(p14 - p16.1),保留了LRPAP1基因的两个拷贝。相反,另一名患者核型为46,XY,del4(p15.3 - pter),在缺失的染色体上未显示LRPAP1的信号。

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