Lamas-Maceiras Mónica, Singh Badri Nath, Hampsey Michael, Freire-Picos María A
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.
J Biol Chem. 2016 Apr 22;291(17):8960-8. doi: 10.1074/jbc.M115.687491. Epub 2016 Feb 29.
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.
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。