SUMO-1 conjugation in vivo requires both a consensus modification motif and nuclear targeting

被引:613
作者
Rodriguez, MS
Dargemont, C
Hay, RT
机构
[1] Univ St Andrews, Sch Biol, St Andrews KY16 9ST, Fife, Scotland
[2] Inst Jacques Monod, Lab Transport Nucleocytoplasm, CNRS UMR 7592, F-75251 Paris 05, France
关键词
D O I
10.1074/jbc.M009476200
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
SUMO-1 is a small ubiquitin-related modifier that is covalently linked to many cellular protein targets. Proteins modified by SUMO-1 and the SUMO-l-activating and -conjugating enzymes are located predominantly in the nucleus. Here we define a transferable sequence containing the psi KXE motif, where psi represents a large hydrophobic amino acid, that confers the ability to be SUMO-l-modified on proteins to which it is linked. Whereas addition of short sequences from p53 and I kappaB alpha containing the psi KXE motif, to a carrier protein is sufficient for modification in vitro, modification in vivo requires the additional presence of a nuclear localization signal. Thus, protein substrates must be targeted to the nucleus to undergo SUMO-1 conjugation.
引用
收藏
页码:12654 / 12659
页数:6
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