A 3′ exonuclease that specifically interacts with the 3′ end of histone mRNA

被引:104
作者
Dominski, Z [1 ]
Yang, XC
Kaygun, H
Dadlez, M
Marzluff, WF
机构
[1] Univ N Carolina, Dept Biochem & Biophys, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Program Mol Biol & Biotechnol, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
[4] Warsaw Univ, Dept Biophys, Polish Acad Sci, Inst Biochem & Biophys, Warsaw, Poland
关键词
D O I
10.1016/S1097-2765(03)00278-8
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
Metazoan histone mRNAs end in a highly conserved stem-loop structure followed by ACCCA. Previous studies have suggested that the stem-loop binding protein (SLBP) is the only protein binding this region. Using RNA affinity purification, we identified a second protein, designated 3'hExo, that contains a SAP and a 3' exonuclease domain and binds the same sequence. Strikingly, 3'hExo can bind the stem-loop region both separately and simultaneously with SLBP. Binding of 3'hExo requires the terminal ACCCA, whereas binding of SLBP requires the 5' side of the stem-loop region. Recombinant 3'hExo degrades RNA substrates in a 3'-5' direction and has the highest activity toward the wild-type histone mRNA. Binding of SLBP to the stem-loop at the 3' end of RNA prevents its degradation by 3'hExo. These features make 3'hExo a primary candidate for the exonuclease that initiates rapid decay of histone mRNA upon completion and/or inhibition of DNA replication.
引用
收藏
页码:295 / 305
页数:11
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