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腺病毒2型L4多聚腺苷酸化结构域的二级结构:在其环中暴露AAUAAA信号的发夹结构的证据。

The secondary structure of the adenovirus-2 L4 polyadenylation domain: evidence for a hairpin structure exposing the AAUAAA signal in its loop.

作者信息

Sittler A, Gallinaro H, Jacob M

机构信息

Institut de Génétique et de Biologie Moléculaire et Cellulaire, UPR 6520 du CNRS, Unité 184 de Biologie Moléculaire et de Génie, Génétique de l'INSERM, Illkirch, France.

出版信息

J Mol Biol. 1995 May 5;248(3):525-40. doi: 10.1006/jmbi.1995.0240.

Abstract

The secondary structure of the adenovirus-2 L4 polyadenylation domain was established using enzymatic attacks and chemical modifications. This domain is characterized by the co-existence of several variants including stem-loop structures of low stability such that its secondary structure is clearly distinct from that of the upstream sequence which harbors large stable hairpin structures. The L4 polyadenylation site is located in a free single-stranded region and the AAUAAA signal is exposed in the 14 nucleotide loop of a hairpin structure with a six-base-pair stem. The 5' arm of this stem includes six nucleotides of a previously identified upstream efficiency element (USEa), whose deletion or substitution reduces cleavage-polyadenylation efficiency by 50%. Several evidences suggest that a signal hairpin structure may be important for polyadenylation. First, the AAUAAA signal is well exposed to enzymes and reagents in its two co-existing variants, suggesting that it is also accessible to cleavage-polyadenylation factors. Second, the disruption of the stem induces a 50% decrease of cleavage efficiency in vitro. Third, the reduction of the size of the loop to five nucleotides reduces cleavage efficiency by 90%. Fourth, polyadenylation domains of other origins can be folded into hairpin structures harboring the AAUAAA signal in their loop. We propose that one of the functions of an upstream efficiency element could be to participate in the presentation of the signal to trans-acting factors.

摘要

通过酶切攻击和化学修饰确定了腺病毒2型L4聚腺苷酸化结构域的二级结构。该结构域的特征是存在多种变体,包括低稳定性的茎环结构,因此其二级结构与含有大的稳定发夹结构的上游序列明显不同。L4聚腺苷酸化位点位于一个自由的单链区域,AAUAAA信号暴露在一个具有六个碱基对茎的发夹结构的14个核苷酸环中。该茎的5'臂包括先前鉴定的上游效率元件(USEa)的六个核苷酸,其缺失或取代会使切割-聚腺苷酸化效率降低50%。多项证据表明,信号发夹结构可能对聚腺苷酸化很重要。首先,AAUAAA信号在其两种共存变体中很好地暴露于酶和试剂中,这表明它也能被切割-聚腺苷酸化因子识别。其次,茎的破坏会导致体外切割效率降低50%。第三,将环的大小减小到五个核苷酸会使切割效率降低90%。第四,其他来源的聚腺苷酸化结构域可以折叠成在其环中含有AAUAAA信号的发夹结构。我们提出,上游效率元件的功能之一可能是参与将信号呈递给反式作用因子。

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