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酿酒酵母中多聚腺苷酸化mRNA、Pab1p、eIF4E和eIF4G与P小体的积累。

Accumulation of polyadenylated mRNA, Pab1p, eIF4E, and eIF4G with P-bodies in Saccharomyces cerevisiae.

作者信息

Brengues Muriel, Parker Roy

机构信息

Department of Molecular and Cellular Biology, Howard Hughes Medical Institute, University of Arizona, Tucson, AZ 85721-0106, USA.

出版信息

Mol Biol Cell. 2007 Jul;18(7):2592-602. doi: 10.1091/mbc.e06-12-1149. Epub 2007 May 2.

DOI:10.1091/mbc.e06-12-1149
PMID:17475768
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1924816/
Abstract

Recent experiments have shown that mRNAs can move between polysomes and P-bodies, which are aggregates of nontranslating mRNAs associated with translational repressors and the mRNA decapping machinery. The transitions between polysomes and P-bodies and how the poly(A) tail and the associated poly(A) binding protein 1 (Pab1p) may affect this process are unknown. Herein, we provide evidence that poly(A)(+) mRNAs can enter P-bodies in yeast. First, we show that both poly(A)(-) and poly(A)(+) mRNA become translationally repressed during glucose deprivation, where mRNAs accumulate in P-bodies. In addition, both poly(A)(+) transcripts and/or Pab1p can be detected in P-bodies during glucose deprivation and in stationary phase. Cells lacking Pab1p have enlarged P-bodies, suggesting that Pab1p plays a direct or indirect role in shifting the equilibrium of mRNAs away from P-bodies and into translation, perhaps by aiding in the assembly of a type of mRNP within P-bodies that is poised to reenter translation. Consistent with this latter possibility, we observed the translation initiation factors (eIF)4E and eIF4G in P-bodies at a low level during glucose deprivation and at high levels in stationary phase. Moreover, Pab1p exited P-bodies much faster than Dcp2p when stationary phase cells were given fresh nutrients. Together, these results suggest that polyadenylated mRNAs can enter P-bodies, and an mRNP complex including poly(A)(+) mRNA, Pab1p, eIF4E, and eIF4G2 may represent a transition state during the process of mRNAs exchanging between P-bodies and translation.

摘要

最近的实验表明,信使核糖核酸(mRNA)可以在多核糖体和P小体之间移动,P小体是与翻译抑制因子和mRNA脱帽机制相关的非翻译mRNA聚集体。多核糖体和P小体之间的转变以及聚腺苷酸(poly(A))尾巴和相关的聚腺苷酸结合蛋白1(Pab1p)如何影响这一过程尚不清楚。在此,我们提供证据表明,聚腺苷酸(poly(A))阳性mRNA可以进入酵母中的P小体。首先,我们表明,在葡萄糖剥夺期间,聚腺苷酸(poly(A))阴性和聚腺苷酸(poly(A))阳性mRNA都会受到翻译抑制,此时mRNA会在P小体中积累。此外,在葡萄糖剥夺期间和稳定期,P小体中都可以检测到聚腺苷酸(poly(A))阳性转录本和/或Pab1p。缺乏Pab1p的细胞具有更大的P小体,这表明Pab1p在将mRNA的平衡从P小体转移到翻译过程中发挥直接或间接作用,可能是通过帮助在P小体中组装一种准备重新进入翻译的mRNA核糖核蛋白(mRNP)。与后一种可能性一致,我们观察到在葡萄糖剥夺期间,翻译起始因子(eIF)4E和eIF4G在P小体中的水平较低,而在稳定期则较高。此外,当给稳定期细胞提供新鲜营养时,Pab1p离开P小体的速度比Dcp2p快得多。总之,这些结果表明,多聚腺苷酸化的mRNA可以进入P小体,并且包括聚腺苷酸(poly(A))阳性mRNA、Pab1p、eIF4E和eIF4G2的mRNP复合物可能代表mRNA在P小体和翻译之间交换过程中的一种过渡状态。

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