Suppr超能文献

由于通过可变剪接从ICAD-L中去除了C末端核定位信号,ICAD-L和ICAD-S在细胞中的定位存在差异。

Differential localization of ICAD-L and ICAD-S in cells due to removal of a C-terminal NLS from ICAD-L by alternative splicing.

作者信息

Samejima K, Earnshaw W C

机构信息

Institute of Cell and Molecular Biology, University of Edinburgh, Edinburgh, Scotland, EH9 3JR, United Kingdom.

出版信息

Exp Cell Res. 2000 Mar 15;255(2):314-20. doi: 10.1006/excr.2000.4801.

Abstract

CAD/CPAN/DFF40 is an apoptotic nuclease that is associated with the regulatory subunit ICAD/DFF in healthy cells. ICAD has two forms, ICAD-L/DFF45 and ICAD-S/DFF35, which are transcribed from a single gene by alternative splicing. They differ at the C-terminus: 70 amino acids of ICAD-L are replaced by 4 different amino acids in ICAD-S. We previously showed that both transfected and endogenous ICAD-L are nuclear; however, the localization of ICAD and CAD remains controversial and an important issue to clarify. Here we present the evidence that ICAD-L is nuclear due to the presence of an autonomous nuclear localization signal located in the C-terminal 20 amino acids. This NLS is missing from ICAD-S, which is distributed throughout the cell. We also showed that a GFP:CAD fusion protein is located in the nucleus of transfected cells.

摘要

CAD/CPAN/DFF40是一种凋亡核酸酶,在健康细胞中与调节亚基ICAD/DFF相关联。ICAD有两种形式,即ICAD-L/DFF45和ICAD-S/DFF35,它们通过可变剪接从单个基因转录而来。它们在C末端有所不同:ICAD-L的70个氨基酸被ICAD-S中的4个不同氨基酸所取代。我们之前表明,转染的和内源性的ICAD-L都位于细胞核中;然而,ICAD和CAD的定位仍存在争议,是一个有待阐明的重要问题。在此我们提供证据表明,ICAD-L定位于细胞核是由于其C末端20个氨基酸中存在一个自主核定位信号。ICAD-S中没有这个核定位信号,它分布于整个细胞中。我们还表明,绿色荧光蛋白:CAD融合蛋白位于转染细胞的细胞核中。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验