Sachdev S, Bruhn L, Sieber H, Pichler A, Melchior F, Grosschedl R
Gene Center and Institute of Biochemistry, University of Munich, 81377 Munich, Germany.
Genes Dev. 2001 Dec 1;15(23):3088-103. doi: 10.1101/gad.944801.
The Wnt-responsive transcription factor LEF1 can activate transcription in association with beta-catenin and repress transcription in association with Groucho. In search of additional regulatory mechanisms of LEF1 function, we identified the protein inhibitor of activated STAT, PIASy, as a novel interaction partner of LEF1. Coexpression of PIASy with LEF1 results in potent repression of LEF1 activity and in covalent modification of LEF1 with SUMO. PIASy markedly stimulates the sumoylation of LEF1 and multiple other proteins in vivo and functions as a SUMO E3 ligase for LEF1 in a reconstituted system in vitro. Moreover, PIASy binds to nuclear matrix-associated DNA sequences and targets LEF1 to nuclear bodies, suggesting that PIASy-mediated subnuclear sequestration accounts for the repression of LEF1 activity.
Wnt反应性转录因子LEF1可与β-连环蛋白结合激活转录,并与Groucho结合抑制转录。为了寻找LEF1功能的其他调控机制,我们鉴定出活化STAT蛋白抑制剂PIASy是LEF1的一种新型相互作用伴侣。PIASy与LEF1共表达可导致LEF1活性的有效抑制以及LEF1的SUMO化共价修饰。PIASy在体内显著刺激LEF1和多种其他蛋白质的SUMO化,并在体外重组系统中作为LEF1的SUMO E3连接酶发挥作用。此外,PIASy与核基质相关的DNA序列结合,并将LEF1靶向至核体,这表明PIASy介导的亚核隔离是LEF1活性受到抑制的原因。