Connelly S, Manley J L
Department of Biological Sciences, Columbia University, New York, New York 10027.
Genes Dev. 1988 Apr;2(4):440-52. doi: 10.1101/gad.2.4.440.
Polyadenylation of pre-mRNAs requires the conserved hexanucleotide AAUAAA, as well as sequences located downstream from the poly(A) addition site. The role of these sequences in the production of functional mRNAs was studied by analyzing a series of mutants containing deletions or substitutions in the SV40 early region poly(A) site. As expected, both a previously defined GU-rich downstream element and an AAUAAA sequence were required for efficient usage of the wild-type poly(A) addition site. However, when either of these elements was deleted, greatly increased levels of SV40-specific RNA were detected in the nuclei of transfected cells. Evidence is presented that this accumulation of RNA resulted from a failure of transcription termination, leading to multiple rounds of transcription of the circular templates. We conclude that the sequences required for efficient cleavage/polyadenylation of the SV40 early pre-mRNA also constitute an important element of an RNA polymerase II termination signal. A model proposing a mechanism by which the act of pre-mRNA 3' end formation is signaled to the elongating RNA polymerase, resulting in termination, is presented.
前体mRNA的聚腺苷酸化需要保守的六核苷酸AAUAAA以及位于聚(A)添加位点下游的序列。通过分析一系列在SV40早期区域聚(A)位点含有缺失或替换的突变体,研究了这些序列在功能性mRNA产生中的作用。正如预期的那样,野生型聚(A)添加位点的有效使用需要先前定义的富含GU的下游元件和AAUAAA序列。然而,当删除这些元件中的任何一个时,在转染细胞的细胞核中检测到SV40特异性RNA水平大幅增加。有证据表明,这种RNA的积累是由于转录终止失败导致环状模板多次转录所致。我们得出结论,SV40早期前体mRNA有效切割/聚腺苷酸化所需的序列也是RNA聚合酶II终止信号的重要组成部分。本文提出了一个模型,该模型提出了一种机制,通过该机制,前体mRNA 3'末端形成的行为被传递给延伸的RNA聚合酶,从而导致终止。