Molecular cloning of novel Monad binding protein containing tetratricopeptide repeat domains

被引:32
作者
Itsuki, Yuki [1 ,3 ]
Saeki, Makio [1 ]
Nakahara, Hirokazu [2 ]
Egusa, Hiroshi [3 ]
Irie, Yasuyuki [4 ]
Terao, Yutaka [5 ]
Kawabata, Shigetada [5 ]
Yatani, Hirofumi [3 ]
Kamisaki, Yoshinori [1 ,6 ]
机构
[1] Osaka Univ, Grad Sch Dent, Dept Pharmacol, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Dept Oral & Maxillofacial Surg 1, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Grad Sch Dent, Dept Fixed Prosthodont, Suita, Osaka 5650871, Japan
[4] Iwate Med Univ, Dept Pharmacol, Morioka, Iwate 020, Japan
[5] Osaka Univ, Grad Sch Dent, Dept Oral & Mol Microbiol, Suita, Osaka 5650871, Japan
[6] Shanghai Univ E Inst, Div Nitr Oxide & Inflammatory Med, Shanghai, Peoples R China
来源
FEBS LETTERS | 2008年 / 582卷 / 16期
基金
日本学术振兴会;
关键词
apoptosis; cell death; caspase; WD repeat; TPR; TNF-alpha;
D O I
10.1016/j.febslet.2008.05.041
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
We have previously reported that Monad, a novel WD40 repeat protein, potentiates apoptosis induced by tumor necrosis factor-alpha(TNF-alpha) and cycloheximide (CHX). By affinity purification and mass spectrometry, we identified RNA polymerase II-associated protein 3 ( RPAP3) as a binding protein of Monad. Overexpression of RPAP3 in HEK 293 potentiated caspase-3 activation and apoptosis induced by TNF-alpha and CHX. In addition, knockdown of RPAP3 by RNA interference resulted in a significant reduction of apoptosis induced by TNF-alpha and CHX in HEK293 and HeLa cells. These results raise the possibility that RPAP3, together with Monad, may function as a novel modulator of apoptosis pathway.
引用
收藏
页码:2365 / 2370
页数:6
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