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II类反式激活因子的GTP结合:在核输入中的作用。

GTP binding by class II transactivator: role in nuclear import.

作者信息

Harton J A, Cressman D E, Chin K C, Der C J, Ting J P

机构信息

Lineberger Comprehensive Cancer Center, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599, USA.

出版信息

Science. 1999 Aug 27;285(5432):1402-5. doi: 10.1126/science.285.5432.1402.

Abstract

Class II transactivator (CIITA) is a global transcriptional coactivator of human leukocyte antigen-D (HLA-D) genes. CIITA contains motifs similar to guanosine triphosphate (GTP)-binding proteins. This report shows that CIITA binds GTP, and mutations in these motifs decrease its GTP-binding and transactivation activity. Substitution of these motifs with analogous sequences from Ras restores CIITA function. CIITA exhibits little GTPase activity, yet mutations in CIITA that confer GTPase activity reduce transcriptional activity. GTP binding by CIITA correlates with nuclear import. Thus, unlike other GTP-binding proteins, CIITA is involved in transcriptional activation that uses GTP binding to facilitate its own nuclear import.

摘要

II类反式激活因子(CIITA)是人类白细胞抗原-D(HLA-D)基因的一种全局转录共激活因子。CIITA含有与鸟苷三磷酸(GTP)结合蛋白相似的基序。本报告表明CIITA结合GTP,且这些基序中的突变会降低其GTP结合和反式激活活性。用来自Ras的类似序列替换这些基序可恢复CIITA功能。CIITA几乎不表现出GTP酶活性,然而赋予GTP酶活性的CIITA突变会降低转录活性。CIITA与GTP的结合与核输入相关。因此,与其他GTP结合蛋白不同,CIITA参与利用GTP结合促进自身核输入的转录激活过程。

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