Transcriptional Activators Enhance Polyadenylation of mRNA Precursors

被引:91
作者
Nagaike, Takashi [1 ]
Logan, Charlotte [1 ]
Hotta, Ikuko [1 ]
Rozenblatt-Rosen, Orit [2 ,3 ]
Meyerson, Matthew [2 ,3 ]
Manley, James L. [1 ]
机构
[1] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[2] Harvard Univ, Dept Med Oncol, Dana Farber Canc Inst, Sch Med, Boston, MA 02115 USA
[3] Harvard Univ, Dept Pathol, Sch Med, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
POLYMERASE-II ELONGATION; 3' UNTRANSLATED REGIONS; B-CELL DIFFERENTIATION; PAF1; COMPLEX; TUMOR-SUPPRESSOR; SACCHAROMYCES-CEREVISIAE; IN-VIVO; GENE-EXPRESSION; HISTONE H3; PROTEIN;
D O I
10.1016/j.molcel.2011.01.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polyadenylation of mRNA precursors is frequently coupled to transcription by RNA polymerase II. Although this coupling is known to involve interactions with the C-terminal domain of the RNA polymerase II largest subunit, the possible role of other factors is not known. Here we show that a prototypical transcriptional activator, GAL4-VP16, stimulates transcription-coupled polyadenylation in vitro. In the absence of GAL4-VP16, specifically initiated transcripts accumulated but little polyadenylation was observed, while in its presence polyadenylation was strongly enhanced. We further show that this stimulation requires the transcription elongation-associated PAF complex (PAF1c), as PAF1c depletion blocked GAL4-VP16-stimulated polyadenylation. Furthermore, knockdown of PAF subunits by siRNA resulted in decreased 3' cleavage, and nuclear export, of mRNA in vivo. Finally, we show that GAL4-VP16 interacts directly with PAF1c and recruits it to DNA templates. Our results indicate that a transcription activator can stimulate transcription-coupled 3' processing and does so via interaction with PAF1c.
引用
收藏
页码:409 / 418
页数:10
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