The deadenylase components Not2p, Not3p, and Not5p promote mRNA decapping

被引:23
作者
Alhusaini, Najwa [1 ]
Coller, Jeff [1 ]
机构
[1] Case Western Reserve Univ, Ctr RNA Mol Biol, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
deadenylation; decapping; mRNA decay; mRNA stability; CCR4-NOT COMPLEX; CAF1; PROTEINS; YEAST; DECAY; MECHANISMS; EXPRESSION; MUTATIONS; MODULE; TRANS;
D O I
10.1261/rna.054742.115
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
Decay of mRNA is essential for the efficient regulation of gene expression. A major pathway of mRNA degradation is initiated by the shortening of the poly(A) tail via the CCR4/NOT deadenylase complex. Deadenylation is followed by removal of the 5' cap (i.e., decapping) and then 5' to 3' exonucleolytic decay of the message body. The highly conserved CCR4/NOT deadenylase complex consists of the exonucleases CCR4 and POP2/CAF1, as well as a group of four or five (depending on organism) accessory factors of unknown function, i.e., the NOT proteins. In this study, we find that Saccharomyces cerevisiae Not2p, Not3p, and Not5p (close paralogs of each other) are involved in promoting mRNA decapping. Furthermore, we find that Not3p and Not5p bind to the decapping activator protein Pat1p. Together, these data implicate the deadenylase complex in coordinating the downstream decapping reaction via Not2p, Not3p, and Not5p. This suggests that the coupling of deadenylation with decapping is, in part, a direct consequence of coordinated assembly of decay factors.
引用
收藏
页码:709 / 721
页数:13
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