Identification of CED-3 substrates by a yeast-based screening method

被引:6
作者
Kim, SY
Valencia, M
Lee, ES
Park, D
Oh, M
Xue, D
Park, WF
机构
[1] Kwangju Inst Sci & Technol, KJIST, Nat Res Lab Proteolysis, Dept Life Sci, Kwangju 500712, South Korea
[2] Univ Colorado, Dept Mol Cellular & Dev Biol, Boulder, CO 80309 USA
关键词
CED-3; substrate; screen; Caenorhabditis elegans; Saccharomyces cerevisiae;
D O I
10.1385/MB:27:1:01
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Identifying cellular substrates repertoire of individual proteases will facilitate our understanding of their physiological and pathological roles. In this article, we employed a yeast-based screening method to isolate CED-3 substrates. This method uses a transcription factor anchored to the plasma membrane by fusion to a library of cellular protein sequences. When a fusion protein is cleaved by CED-3, the transcription-factor is released from the plasma membrane and enters the nucleus where it turns on the expression of reporter genes. We identified seven candidate clones by screening a genomic library using this method. Of these seven clones, two were cleaved by purified CED-3 invitro. Therefore, the method described here may be generally used for genomewide screening to isolate potential substrates of specific proteases.
引用
收藏
页码:1 / 6
页数:6
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