首页> 美国卫生研究院文献>Journal of Virology >A small deletion distant from a splice or polyadenylation site dramatically alters pre-mRNA processing in region E3 of adenovirus.
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A small deletion distant from a splice or polyadenylation site dramatically alters pre-mRNA processing in region E3 of adenovirus.

机译:远离剪接或聚腺苷酸化位点的小缺失会显着改变腺病毒E3区域中的前mRNA加工。

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摘要

The E3 complex transcription unit of adenovirus encodes overlapping mRNAs (a to i) with different exon structures. The major mRNAs are a (approximately 40% of the total) and c (approximately 15%), which are spliced once, and f (approximately 15%) and h (approximately 25%), which are spliced twice. mRNA a uses the upstream E3A polyadenylation site, and the other mRNAs use the downstream E3B polyadenylation site. We analyzed virus deletion mutants to identify sequences important in alternative pre-mRNA processing in region E3. Our main finding is that a 64-base-pair deletion in dl742 causes mainly mRNAs f and h to be formed. mRNAs a and c are barely made. dl742 does not delete either a splice site or a polyadenylation site. Thus, the sequences deleted must function in alternative pre-mRNA processing independently of the signals at the actual splice and polyadenylation sites. The lack of synthesis of mRNA a by dl742 does not appear to result from a defect in the E3A polyadenylation signal but rather from an increase in splicing activity which results in the synthesis of doubly spliced mRNAs f and h at the expense of singly spliced mRNAs a and c. This suggests, in the wild-type situation, that the frequency of use of the E3A versus the E3B polyadenylation site may be determined by the rate of splicing, as well as, presumably, the rate of cleavage-polyadenylation at the E3A site.
机译:腺病毒的E3复合物转录单位编码具有不同外显子结构的重叠mRNA(从a到i)。主要的mRNA是a(约占总数的40%)和c(约15%),它们被剪接一次,以及f(约占15%)和h(约25%),它们剪接了两次。 mRNA a使用上游E3A聚腺苷酸化位点,其他mRNA使用下游E3B聚腺苷酸化位点。我们分析了病毒缺失突变体,以鉴定在区域E3的替代前mRNA处理中重要的序列。我们的主要发现是dl742中64个碱基对的缺失主要导致mRNA的形成。 mRNA a和c几乎没有。 dl742不会删除剪接位点或聚腺苷酸化位点。因此,删除的序列必须在替代的前mRNA处理中发挥作用,而与实际剪接和聚腺苷酸化位点的信号无关。 dl742缺乏mRNA的合成似乎不是由于E3A聚腺苷酸化信号的缺陷引起的,而是由于剪接活性的增加,从而导致了双剪接的mRNA f和h的合成,但单剪接的mRNA a却受到了损害。和c。这表明,在野生型情况下,E3A相对于E3B聚腺苷酸化位点的使用频率可以由剪接速率以及大概在E3A位置的裂解-聚腺苷酸化率来确定。

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