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The Ssu72 phosphatase mediates the RNA polymerase II initiation-elongation transition.Ssu72磷酸酶介导RNA聚合酶II起始-延伸转换。
J Biol Chem. 2014 Dec 5;289(49):33916-26. doi: 10.1074/jbc.M114.608695. Epub 2014 Oct 22.
2
RBBP6 isoforms regulate the human polyadenylation machinery and modulate expression of mRNAs with AU-rich 3' UTRs.RBBP6 亚型调节人类多聚腺苷酸化机制,并调节具有富含 AU 的 3' UTR 的 mRNA 的表达。
Genes Dev. 2014 Oct 15;28(20):2248-60. doi: 10.1101/gad.245787.114.
3
Alternative polyadenylation in the nervous system: to what lengths will 3' UTR extensions take us?神经系统中的可变多聚腺苷酸化:3'UTR 延长将引领我们走向何方?
Bioessays. 2014 Aug;36(8):766-77. doi: 10.1002/bies.201300174. Epub 2014 Jun 5.
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Means to an end: mechanisms of alternative polyadenylation of messenger RNA precursors.达成目的之手段:信使核糖核酸前体的可变聚腺苷酸化机制
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Ubiquitously transcribed genes use alternative polyadenylation to achieve tissue-specific expression.普遍转录基因通过选择性聚腺苷酸化实现组织特异性表达。
Genes Dev. 2013 Nov 1;27(21):2380-96. doi: 10.1101/gad.229328.113. Epub 2013 Oct 21.
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UV damage regulates alternative polyadenylation of the RPB2 gene in yeast.紫外线损伤调控酵母中 RPB2 基因的可变多聚腺苷酸化。
Nucleic Acids Res. 2013 Mar 1;41(5):3104-14. doi: 10.1093/nar/gkt020. Epub 2013 Jan 25.
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Disengaging polymerase: terminating RNA polymerase II transcription in budding yeast.脱离聚合酶:在芽殖酵母中终止RNA聚合酶II转录
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8
Gene loops enhance transcriptional directionality.基因环增强转录方向。
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9
The yeast regulator of transcription protein Rtr1 lacks an active site and phosphatase activity.酵母转录调控蛋白 Rtr1 缺乏活性位点和磷酸酶活性。
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10
A universal RNA polymerase II CTD cycle is orchestrated by complex interplays between kinase, phosphatase, and isomerase enzymes along genes.一个通用的 RNA 聚合酶 II CTD 循环是由激酶、磷酸酶和异构酶等酶沿着基因进行复杂相互作用来协调的。
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启动子-终止子基因环影响酵母中3'端加工的选择性过程。

Promoter-Terminator Gene Loops Affect Alternative 3'-End Processing in Yeast.

作者信息

Lamas-Maceiras Mónica, Singh Badri Nath, Hampsey Michael, Freire-Picos María A

机构信息

From the Departamento de Biología Celular e Molecular, Facultad de Ciencias, Universidade da Coruña, Campus de A Coruña, Rúa da Fraga 10, 15008 A Coruña, Spain and.

the Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers University, Piscataway, New Jersey 08854.

出版信息

J Biol Chem. 2016 Apr 22;291(17):8960-8. doi: 10.1074/jbc.M115.687491. Epub 2016 Feb 29.

DOI:10.1074/jbc.M115.687491
PMID:26929407
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4861464/
Abstract

Many eukaryotic genes undergo alternative 3'-end poly(A)-site selection producing transcript isoforms with 3'-UTRs of different lengths and post-transcriptional fates. Gene loops are dynamic structures that juxtapose the 3'-ends of genes with their promoters. Several functions have been attributed to looping, including memory of recent transcriptional activity and polarity of transcription initiation. In this study, we investigated the relationship between gene loops and alternative poly(A)-site. Using the KlCYC1 gene of the yeast Kluyveromyces lactis, which includes a single promoter and two poly(A) sites separated by 394 nucleotides, we demonstrate in two yeast species the formation of alternative gene loops (L1 and L2) that juxtapose the KlCYC1 promoter with either proximal or distal 3'-end processing sites, resulting in the synthesis of short and long forms of KlCYC1 mRNA. Furthermore, synthesis of short and long mRNAs and formation of the L1 and L2 loops are growth phase-dependent. Chromatin immunoprecipitation experiments revealed that the Ssu72 RNA polymerase II carboxyl-terminal domain phosphatase, a critical determinant of looping, peaks in early log phase at the proximal poly(A) site, but as growth phase advances, it extends to the distal site. These results define a cause-and-effect relationship between gene loops and alternative poly(A) site selection that responds to different physiological signals manifested by RNA polymerase II carboxyl-terminal domain phosphorylation status.

摘要

许多真核基因会进行3'端多聚腺苷酸化位点的选择性使用,从而产生具有不同长度3'非翻译区(3'-UTR)和转录后命运的转录本异构体。基因环是一种动态结构,它将基因的3'端与其启动子并列在一起。环化作用具有多种功能,包括对近期转录活性的记忆以及转录起始的极性。在本研究中,我们探究了基因环与选择性多聚腺苷酸化位点之间的关系。利用乳酸克鲁维酵母的KlCYC1基因,该基因包含一个单一启动子和两个被394个核苷酸隔开的多聚腺苷酸化位点,我们在两种酵母物种中证明了选择性基因环(L1和L2)的形成,这些环将KlCYC1启动子与近端或远端3'端加工位点并列在一起,从而导致短形式和长形式的KlCYC1 mRNA的合成。此外,短mRNA和长mRNA的合成以及L1和L2环的形成均依赖于生长阶段。染色质免疫沉淀实验表明,Ssu72 RNA聚合酶II羧基末端结构域磷酸酶是环化作用的关键决定因素,它在对数早期近端多聚腺苷酸化位点处达到峰值,但随着生长阶段的推进,它会延伸至远端位点。这些结果确定了基因环与选择性多聚腺苷酸化位点选择之间的因果关系,这种关系对由RNA聚合酶II羧基末端结构域磷酸化状态所表现出的不同生理信号作出响应。