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翻译过程中的RNA解旋:包含真核生物起始因子eIF-4F和eIF-4B的解旋酶复合中间体的组装。

RNA unwinding in translation: assembly of helicase complex intermediates comprising eukaryotic initiation factors eIF-4F and eIF-4B.

作者信息

Jaramillo M, Dever T E, Merrick W C, Sonenberg N

机构信息

Department of Biochemistry, McGill University, Montreal, Quebec, Canada.

出版信息

Mol Cell Biol. 1991 Dec;11(12):5992-7. doi: 10.1128/mcb.11.12.5992-5997.1991.

DOI:10.1128/mcb.11.12.5992-5997.1991
PMID:1719376
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC361763/
Abstract

Ribosome binding to mRNA requires the concerted action of three initiation factors, eIF-4A, eIF-4B, and eIF-4F, and the hydrolysis of ATP in a mechanism that is not well understood. Several lines of evidence support a model by which these factors bind to the 5' end of mRNA and unwind proximal secondary structure, thus allowing 40S ribosomal subunits to bind. We have previously used an unwinding assay to demonstrate that eIF-4A or eIF-4F in combination with eIF-4B functions as an RNA helicase. To elucidate the molecular mechanism of RNA unwinding, we used a mobility shift electrophoresis assay which allows the simultaneous analysis of unwinding and complex formation between these factors and RNA. eIF-4F forms a stable complex (complex A) with duplex RNA in the absence of ATP. Addition of eIF-4B results in the formation of a second complex (complex B) of slower mobility in the gel. In the presence of ATP, both complexes dissociate, concomitant with the unwinding of the duplex RNA. We present evidence to suggest that unwinding occurs in a processive as opposed to distributive manner. Thus, we conclude that helicase complexes that are formed in the absence of ATP on duplex RNA translocate processively along the RNA in an ATP-dependent reaction and melt secondary structure. These helicase complexes therefore represent intermediates in the unwinding process of mRNA that could precede ribosome binding.

摘要

核糖体与mRNA的结合需要三种起始因子(eIF-4A、eIF-4B和eIF-4F)协同作用,以及ATP水解,但其机制尚不清楚。几条证据支持这样一种模型,即这些因子与mRNA的5'端结合并解开近端二级结构,从而使40S核糖体亚基能够结合。我们之前使用解旋分析来证明eIF-4A或eIF-4F与eIF-4B结合后可作为RNA解旋酶发挥作用。为了阐明RNA解旋的分子机制,我们使用了迁移率变动电泳分析,该分析能够同时分析这些因子与RNA之间的解旋和复合物形成情况。在没有ATP的情况下,eIF-4F与双链RNA形成稳定的复合物(复合物A)。添加eIF-4B会导致在凝胶中形成迁移率较慢的第二种复合物(复合物B)。在有ATP的情况下,两种复合物都会解离,同时双链RNA解旋。我们提供的证据表明,解旋是以持续性而非分布性方式发生的。因此,我们得出结论,在双链RNA上无ATP时形成的解旋酶复合物在ATP依赖性反应中沿RNA进行性移位并解开二级结构。因此,这些解旋酶复合物代表了mRNA解旋过程中可能先于核糖体结合的中间体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a748/361763/468b5f4210ff/molcellb00036-0208-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a748/361763/58ceed52d090/molcellb00036-0206-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a748/361763/0734c7783c6c/molcellb00036-0206-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a748/361763/ffb31f04162b/molcellb00036-0207-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a748/361763/8645284ccec3/molcellb00036-0207-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a748/361763/468b5f4210ff/molcellb00036-0208-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a748/361763/58ceed52d090/molcellb00036-0206-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a748/361763/0734c7783c6c/molcellb00036-0206-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a748/361763/ffb31f04162b/molcellb00036-0207-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a748/361763/8645284ccec3/molcellb00036-0207-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a748/361763/468b5f4210ff/molcellb00036-0208-a.jpg

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