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

机译:腺苷酸酶成分Not2p,Not3p和Not5p促进mRNA脱盖

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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.
机译:mRNA的衰变对于基因表达的有效调节至关重要。 mRNA降解的主要途径是通过CCR4 / NOT腺苷酸酶复合物缩短poly(A)尾部而引发的。腺苷酸化之后,除去5'帽(即脱盖),然后除去信息主体的5'至3'核酸外切变。高度保守的CCR4 / NOT腺苷酸酶复合物由核酸外切酶CCR4和POP2 / CAF1,以及由4或5个(取决于生物体)功能未知的辅助因子(即NOT蛋白)组成。在这项研究中,我们发现啤酒酵母Not2p,Not3p和Not5p(彼此的近旁系同源物)参与促进mRNA脱盖。此外,我们发现Not3p和Not5p绑定到去盖激活蛋白Pat1p。总之,这些数据暗示了腺苷酸酶复合物通过Not2p,Not3p和Not5p协调下游的脱盖反应。这表明,去甲腺苷酸化与去壳化的结合部分是衰变因子协调装配的直接结果。

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