首页> 美国卫生研究院文献>The EMBO Journal >Splice site selection dominates over poly(A) site choice in RNA production from complex adenovirus transcription units.
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Splice site selection dominates over poly(A) site choice in RNA production from complex adenovirus transcription units.

机译:在复杂腺病毒转录单位的RNA生产中剪接位点选择比poly(A)位点选择起主导作用。

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摘要

The adenovirus late genes are organized in a complex transcription unit in which the production of multiple RNAs is controlled by specific RNA processing events. Adding to the complexity is the fact that the early E3 transcription unit is wholly contained within the late transcription unit. Within this overlapping region there are splicing events and poly(A) site choices specific to each transcription unit. Early in infection, there is near exclusive use of the E3 splice sites with little L4 poly(A) site use whereas the reverse is true late in infection. Using a plasmid containing an intact E3 transcription unit, we demonstrate that the L4 poly(A) site, located in the first E3 intron, is not used either in a mock-infected cell or a late infected cell; nor is it used if the same transcription unit is driven by the major late promoter. In addition, the nature of the poly(A) site appeared to be unimportant since the E3 poly(A) site was also not used in the intron if inserted in place of the L4 poly(A) site. Thus, splice site selection appears to dominate over poly(A) site choice. This conclusion was confirmed by the observation that deletion of either the E3 splice donor (5'ss) or the E3 splice acceptor (3'ss) allowed the use of the L4 poly(A) site. Finally, the L4 poly(A) site within the E3 intron was also used when additional sequence, including splicing signals from the L4 region and the tripartite leader, was inserted between the promoter and the E3 processing sites. It appears that splicing is the dominant event in governing production of E3/L4 RNAs.
机译:腺病毒晚期基因被组织在一个复杂的转录单元中,其中多个RNA的产生由特定的RNA加工事件控制。复杂的事实是,早期的E3转录单元完全包含在后期的转录单元中。在该重叠区域内,存在每个转录单位特有的剪接事件和poly(A)位点选择。在感染早期,几乎不使用E3剪接位点,而很少使用L4 poly(A)位点,而在感染晚期则相反。使用含有完整E3转录单位的质粒,我们证明了位于第一个E3内含子中的L4 poly(A)位点在模拟感染细胞或晚期感染细胞中均未使用。如果相同的转录单位由主要的晚期启动子驱动,也不会使用。另外,poly(A)位点的性质似乎并不重要,因为如果插入L4 poly(A)位点,E3 poly(A)位点也未用于内含子。因此,拼接位点的选择似乎胜过poly(A)位点的选择。通过观察到以下结论证实了这一结论:E3剪接供体(5's)或E3剪接受体(3's)的删除允许使用L4 poly(A)位点。最后,当在启动子和E3加工位点之间插入其他序列(包括来自L4区和三联前导序列的剪接信号)时,也使用了E3内含子内的L4 poly(A)位点。似乎剪接是控制E3 / L4 RNA产生的主要事件。

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