Genomic organization and cloning of the human homologue of murine Sipa-1

被引:1
|
作者
Ebrahimi, S
Wang, E
Udar, N
Arnold, E
Burbee, D
Small, K
Sawicki, MP
机构
[1] Univ Calif Los Angeles, Sch Med, Los Angeles, CA 90095 USA
[2] W Los Angeles Vet Affairs Med Ctr, Dept Surg, Core Mol Biol Unit, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Los Angeles, CA 90095 USA
[4] Univ Texas, Hammond Ctr Therapeut Oncol Res, Dallas, TX 75235 USA
关键词
GTPase activating protein; chromosome; 11q13; tumor suppressor gene; multiple endocrine neoplasia type 1;
D O I
10.1016/S0378-1119(98)00212-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Murine Sipa-1 (signal-induced proliferation associated protein) is a mitogen induced GTPase activating protein (GAP). While mapping candidate genes for multiple endocrine neoplasia type 1 (MEN1) at 11q13, we cloned the human homologue of Sipa-1. Herein, we report the complete cDNA sequence, expression, and genomic organization of SIPA-1. SIPA-1 consists of 16 exons with highly conserved exon-intron boundaries. The predicted SIPA-1 protein is highly homologous to the mouse protein, particularly in the region of the GAP-related domain at the amino terminus and the leucine zipper at the carboxy terminus. It is widely expressed, including in fetal tissues, but is most highly expressed in lymphoid organs. During the course of cloning SIPA-1, the MEN1 gene was identified, thus excluding human SIPA-1 as a candidate for this disease. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:215 / 221
页数:7
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