School of Biosciences, University of Birmingham, Edgbaston, Birmingham, United Kingdom.
Mol Cell Biol. 2011 Feb;31(4):639-51. doi: 10.1128/MCB.00919-10. Epub 2010 Dec 6.
Poly(A) signals located at the 3' end of eukaryotic genes drive cleavage and polyadenylation at the same end of pre-mRNA. Although these sequences are expected only at the 3' end of genes, we found that strong poly(A) signals are also predicted within the 5' untranslated regions (UTRs) of many Drosophila melanogaster mRNAs. Most of these 5' poly(A) signals have little influence on the processing of the endogenous transcripts, but they are very active when placed at the 3' end of reporter genes. In investigating these unexpected observations, we discovered that both these novel poly(A) signals and standard poly(A) signals become functionally silent when they are positioned close to transcription start sites in either Drosophila or human cells. This indicates that the stage when the poly(A) signal emerges from the polymerase II (Pol II) transcription complex determines whether a putative poly(A) signal is recognized as functional. The data suggest that this mechanism, which probably prevents cryptic poly(A) signals from causing premature transcription termination, depends on low Ser2 phosphorylation of the C-terminal domain of Pol II and inefficient recruitment of processing factors.
真核基因 3' 末端的多聚(A)信号驱动前体 mRNA 在同一末端的切割和多聚腺苷酸化。尽管这些序列仅预期位于基因的 3' 末端,但我们发现许多黑腹果蝇 mRNAs 的 5' 非翻译区(UTR)中也预测到了强多聚(A)信号。这些 5' 多聚(A)信号中的大多数对内源性转录物的加工几乎没有影响,但当它们位于报告基因的 3' 末端时,它们非常活跃。在研究这些意外观察结果时,我们发现,无论是在果蝇还是人类细胞中,这些新的多聚(A)信号和标准的多聚(A)信号在靠近转录起始位点时都会失去功能。这表明多聚(A)信号从聚合酶 II(Pol II)转录复合物中出现的阶段决定了一个假定的多聚(A)信号是否被识别为功能信号。这些数据表明,这种机制可能防止隐匿的多聚(A)信号导致过早的转录终止,这取决于 Pol II C 末端结构域的低 Ser2 磷酸化和加工因子的低效募集。