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编码一种位于中心体的A激酶锚定蛋白AKAP450的cDNA的克隆与鉴定

Cloning and characterization of a cDNA encoding an A-kinase anchoring protein located in the centrosome, AKAP450.

作者信息

Witczak O, Skålhegg B S, Keryer G, Bornens M, Taskén K, Jahnsen T, Orstavik S

机构信息

Institute of Medical Biochemistry, Faculty of Medicine, University of Oslo, PO Box 1112, Blindern N-0317 Oslo, Norway.

出版信息

EMBO J. 1999 Apr 1;18(7):1858-68. doi: 10.1093/emboj/18.7.1858.

Abstract

A combination of protein kinase A type II (RII) overlay screening, database searches and PCR was used to identify a centrosomal A-kinase anchoring protein. A cDNA with an 11.7 kb open reading frame was characterized and found to correspond to 50 exons of genomic sequence on human chromosome 7q21-22. This cDNA clone encoded a 3908 amino acid protein of 453 kDa, that was designated AKAP450 (DDBJ/EMBL/GenBank accession No. AJ131693). Sequence comparison demonstrated that the open reading frame contained a previously characterized cDNA encoding Yotiao, as well as the human homologue of AKAP120. Numerous coiled-coil structures were predicted from AKAP450, and weak homology to pericentrin, giantin and other structural proteins was observed. A putative RII-binding site was identified involving amino acid 2556 of AKAP450 by mutation analysis combined with RII overlay and an amphipatic helix was predicted in this region. Immunoprecipitation of RII from RIPA-buffer extracts of HeLa cells demonstrated co-precipitation of AKAP450. By immunofluorecent labeling with specific antibodies it was demonstrated that AKAP450 localized to centrosomes. Furthermore, AKAP450 was shown to co-purify in centrosomal preparations. The observation of two mRNAs and several splice products suggests additional functions for the AKAP450 gene.

摘要

通过蛋白激酶A II型(RII)覆盖筛选、数据库搜索和聚合酶链反应(PCR)相结合的方法,鉴定出一种中心体A激酶锚定蛋白。对一个具有11.7 kb开放阅读框的cDNA进行了表征,发现它对应于人类染色体7q21 - 22上基因组序列的50个外显子。该cDNA克隆编码一个由3908个氨基酸组成、分子量为453 kDa的蛋白质,命名为AKAP450(DDBJ/EMBL/GenBank登录号:AJ131693)。序列比较表明,该开放阅读框包含一个先前已表征的编码Yotiao的cDNA,以及AKAP120的人类同源物。从AKAP450预测出许多卷曲螺旋结构,并观察到与中心粒蛋白、巨蛋白和其他结构蛋白的弱同源性。通过突变分析结合RII覆盖,在AKAP450的2556位氨基酸处鉴定出一个假定的RII结合位点,并在该区域预测出一个两亲性螺旋。从HeLa细胞的RIPA缓冲液提取物中免疫沉淀RII,结果表明AKAP450共沉淀。用特异性抗体进行免疫荧光标记表明,AKAP450定位于中心体。此外,在中心体制备物中显示AKAP450能共纯化。观察到两种mRNA和几种剪接产物,提示AKAP450基因具有其他功能。

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