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A functional interaction between Rev and yeast pre-mRNA is related to splicing complex formation.

作者信息

Stutz F, Rosbash M

机构信息

Howard Hughes Medical Institute, Department of Biology, Brandeis University, Waltham, MA 02254.

出版信息

EMBO J. 1994 Sep 1;13(17):4096-104. doi: 10.1002/j.1460-2075.1994.tb06727.x.

DOI:10.1002/j.1460-2075.1994.tb06727.x
PMID:8076605
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC395332/
Abstract

The HIV-1 Rev protein regulates viral gene expression by enhancing the export of partially spliced or nonspliced viral transcripts to the cytoplasm. This activity is mediated by the interaction of Rev with a highly structured viral RNA sequence, the Rev response element (RRE). In this paper, Rev regulation has been recapitulated in the yeast Saccharomyces cerevisiae. The data show that Rev enhances yeast pre-mRNA translation in an RRE-dependent manner and requires intact RNA binding and effector domains. In addition, reporter gene mutations in the 5' splice site and in the branch point are epistatic to and eliminate Rev responsiveness, i.e. some spliceosome assembly pathway steps precede a functional interaction with Rev. The results indicate that some of the Rev-interacting components are conserved between yeast and mammals and suggest that Rev acts on yeast pre-mRNA in the context of the spliceosome.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe6/395332/165808d7cac8/emboj00065-0182-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe6/395332/a8d47530de5b/emboj00065-0179-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe6/395332/7d0e7288431d/emboj00065-0180-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe6/395332/9fa8ea8002dc/emboj00065-0181-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe6/395332/3695c71a9204/emboj00065-0182-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe6/395332/165808d7cac8/emboj00065-0182-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe6/395332/a8d47530de5b/emboj00065-0179-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe6/395332/7d0e7288431d/emboj00065-0180-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe6/395332/9fa8ea8002dc/emboj00065-0181-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe6/395332/3695c71a9204/emboj00065-0182-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fe6/395332/165808d7cac8/emboj00065-0182-b.jpg

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1
A functional interaction between Rev and yeast pre-mRNA is related to splicing complex formation.
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The basic domain of Rev from human immunodeficiency virus type 1 specifically blocks the entry of U4/U6.U5 small nuclear ribonucleoprotein in spliceosome assembly.来自1型人类免疫缺陷病毒的Rev基本结构域特异性地阻断U4/U6.U5小核核糖核蛋白进入剪接体组装过程。
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Mol Cell Biol. 1996 Dec;16(12):7144-50. doi: 10.1128/MCB.16.12.7144.

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本文引用的文献

1
Mutational analysis of pre-mRNA splicing in Saccharomyces cerevisiae using a sensitive new reporter gene, CUP1.利用一种灵敏的新报告基因CUP1对酿酒酵母前体mRNA剪接进行突变分析。
Genetics. 1993 Apr;133(4):851-63. doi: 10.1093/genetics/133.4.851.
2
The basic domain of Rev from human immunodeficiency virus type 1 specifically blocks the entry of U4/U6.U5 small nuclear ribonucleoprotein in spliceosome assembly.来自1型人类免疫缺陷病毒的Rev基本结构域特异性地阻断U4/U6.U5小核核糖核蛋白进入剪接体组装过程。
J Virol. 1993 Aug;67(8):4769-76. doi: 10.1128/JVI.67.8.4769-4776.1993.
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Human immunodeficiency virus env expression becomes Rev-independent if the env region is not defined as an intron.
Viruses. 2015 Aug 4;7(8):4326-51. doi: 10.3390/v7082822.
4
Yeast Tdh3 (glyceraldehyde 3-phosphate dehydrogenase) is a Sir2-interacting factor that regulates transcriptional silencing and rDNA recombination.酵母 Tdh3(甘油醛-3-磷酸脱氢酶)是一种与 Sir2 相互作用的因子,可调节转录沉默和 rDNA 重组。
PLoS Genet. 2013;9(10):e1003871. doi: 10.1371/journal.pgen.1003871. Epub 2013 Oct 17.
5
Trans-packaging of human immunodeficiency virus type 1 genome into Gag virus-like particles in Saccharomyces cerevisiae.在酿酒酵母中,将人类免疫缺陷病毒 1 基因组进行包裹,形成 Gag 病毒样颗粒。
Microb Cell Fact. 2013 Mar 26;12:28. doi: 10.1186/1475-2859-12-28.
6
The biflavonoid isoginkgetin is a general inhibitor of Pre-mRNA splicing.双黄酮异银杏双黄酮是前体mRNA剪接的通用抑制剂。
J Biol Chem. 2008 Nov 28;283(48):33147-54. doi: 10.1074/jbc.M805556200. Epub 2008 Sep 30.
7
Saccharomyces cerevisiae: a versatile eukaryotic system in virology.酿酒酵母:病毒学中的一种多功能真核系统。
Microb Cell Fact. 2007 Oct 10;6:32. doi: 10.1186/1475-2859-6-32.
8
The strength of the HIV-1 3' splice sites affects Rev function.HIV-1 3'剪接位点的强度会影响Rev功能。
Retrovirology. 2006 Dec 4;3:89. doi: 10.1186/1742-4690-3-89.
9
The sequence complementarity between HIV-1 5' splice site SD4 and U1 snRNA determines the steady-state level of an unstable env pre-mRNA.HIV-1 5'剪接位点SD4与U1小核核糖核酸(snRNA)之间的序列互补性决定了不稳定的env前体信使核糖核酸(pre-mRNA)的稳态水平。
RNA. 2001 Mar;7(3):421-34. doi: 10.1017/s1355838201001212.
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Multiple portions of poly(A)-binding protein stimulate translation in vivo.多聚腺苷酸结合蛋白的多个部分在体内刺激翻译。
EMBO J. 2000 Sep 1;19(17):4723-33. doi: 10.1093/emboj/19.17.4723.
如果env区域未被定义为内含子,人类免疫缺陷病毒env表达将变得不依赖于Rev。
J Virol. 1994 Feb;68(2):951-8. doi: 10.1128/JVI.68.2.951-958.1994.
4
Rev and the fate of pre-mRNA in the nucleus: implications for the regulation of RNA processing in eukaryotes.Rev与细胞核内前体mRNA的命运:对真核生物RNA加工调控的影响
Mol Cell Biol. 1993 Oct;13(10):6180-9. doi: 10.1128/mcb.13.10.6180-6189.1993.
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Evidence that HIV-1 Rev directly promotes the nuclear export of unspliced RNA.有证据表明,HIV-1 Rev直接促进未剪接RNA的核输出。
EMBO J. 1994 Sep 1;13(17):4105-12. doi: 10.1002/j.1460-2075.1994.tb06728.x.
6
Primary structure and transcription of an amplified genetic locus: the CUP1 locus of yeast.一个扩增基因位点的一级结构与转录:酵母的 CUP1 位点
Proc Natl Acad Sci U S A. 1984 Jan;81(2):337-41. doi: 10.1073/pnas.81.2.337.
7
Transformation of intact yeast cells treated with alkali cations.经碱金属阳离子处理的完整酵母细胞的转化
J Bacteriol. 1983 Jan;153(1):163-8. doi: 10.1128/jb.153.1.163-168.1983.
8
Expression of a beta-galactosidase gene containing the ribosomal protein 51 intron is sensitive to the rna2 mutation of yeast.含有核糖体蛋白51内含子的β-半乳糖苷酶基因的表达对酵母的rna2突变敏感。
Proc Natl Acad Sci U S A. 1983 Jul;80(14):4403-7. doi: 10.1073/pnas.80.14.4403.
9
Tandem gene amplification mediates copper resistance in yeast.串联基因扩增介导酵母中的铜抗性。
Proc Natl Acad Sci U S A. 1982 Sep;79(17):5342-6. doi: 10.1073/pnas.79.17.5342.
10
Expression of heterologous genes in Saccharomyces cerevisiae from vectors utilizing the glyceraldehyde-3-phosphate dehydrogenase gene promoter.利用甘油醛-3-磷酸脱氢酶基因启动子的载体在酿酒酵母中表达异源基因。
Gene. 1984 Dec;32(3):263-74. doi: 10.1016/0378-1119(84)90002-7.