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Flexibility and interchangeability of polyadenylation signals in Saccharomyces cerevisiae.

机译:酿酒酵母中聚腺苷酸化信号的灵活性和互换性。

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Various signal motifs have been reported to be essential for proper mRNA 3'-end formation in the yeast Saccharomyces cerevisiae. However, none of these motifs has been shown to be sufficient to direct 3'-end processing and/or transcription termination. Therefore, several structural motifs have to act in concert for efficient 3'-end formation. In the region upstream of the three polyadenylation sites of the yeast gene for alcohol dehydrogenase I (ADH1), we have identified a hitherto unknown signal sequence contained within the octamer AAAAAAAA. This motif, located 11 nucleotides upstream of the first ADH1 polyadenylation site, is responsible for the utilization of this site in vitro and in vivo, since mutational alteration drastically reduced 3'-end formation at this position. Insertion of 38 ADH1-derived nucleotides encompassing the (A)8 motif into the 3'-end formation-deficient cyc1-512 deletion mutant restored full processing capacity in vitro. Insertion of the octamer alone did not restore 3'-end formation, although mutation of the (A)8 motif in the functional construct had abolished 3'-end processing activity almost completely. This demonstrates that the sequence AAAAAAAA is a necessary, although not sufficient, signal for efficient mRNA 3'-end formation in S. cerevisiae.
机译:据报道,各种信号基序对于酿酒酵母中正确的mRNA 3'-端形成是必不可少的。但是,这些基序均未显示足以指导3'-末端加工和/或转录终止。因此,为了有效地形成3'-末端,必须协同作用多个结构基序。在酒精脱氢酶I(ADH1)酵母基因的三个聚腺苷酸化位点上游区域,我们确定了八聚体AAAAAAAA中迄今未知的信号序列。该基序位于第一个ADH1聚腺苷酸化位点上游11个核苷酸处,负责在体外和体内利用该位点,因为突变改变大大减少了该位置的3'端形成。将包含(A)8基序的38个ADH1衍生核苷酸插入3'-末端形成缺陷的cyc1-512缺失突变体可恢复体外的全部加工能力。单独插入八聚体并不能恢复3'-末端的形成,尽管功能性构建物中(A)8基序的突变几乎完全消除了3'-末端的加工活性。这表明序列AAAAAAAA是酿酒酵母中有效的mRNA 3'末端形成的必要但不是充分的信号。

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