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多瘤病毒DNA区域中对基因表达重要的序列重复。

Sequence repeats in a polyoma virus DNA region important for gene expression.

作者信息

Ruley H E, Fried M

出版信息

J Virol. 1983 Jul;47(1):233-7. doi: 10.1128/JVI.47.1.233-237.1983.

Abstract

The sequenced prototype strains (A2 and A3) of polyoma virus lack sequence duplications characteristic of other papovaviruses. However, we found that five polyoma virus strains (P16, Toronto large plaque, MV, Ts 48, and NG59R) contain tandemly duplicated sequences in a region near the late RNA leader. Although the duplications vary in size (31 to 84 base pairs) and location (between nucleotide [nt] 5068 and nt 5185), the sequence between nt 5114 and nt 5137 is contained within all five duplicated segments. This region is known to be important in polyoma virus early gene expression, and it contains sequences capable of enhancing the expression of nonviral genes. Inspection of the sequences at and around the ends of the repeats indicated that the duplications do not arise by homologous recombination, and there was no indication that a sequence-specific mechanism results in their formation. However, the variation in the structure of the repeats among different polyoma virus strains suggests that these sequence duplications are a recent evolutionary occurrence. The potential biological significance of this variation is discussed.

摘要

多瘤病毒的测序原型毒株(A2和A3)缺乏其他乳头瘤多瘤空泡病毒科病毒所特有的序列重复特征。然而,我们发现五种多瘤病毒毒株(P16、多伦多大型噬菌斑毒株、MV、Ts 48和NG59R)在晚期RNA前导序列附近的区域含有串联重复序列。尽管这些重复序列的大小(31至84个碱基对)和位置(在核苷酸[nt]5068和nt 5185之间)有所不同,但nt 5114和nt 5137之间的序列包含在所有五个重复片段中。已知该区域在多瘤病毒早期基因表达中很重要,并且它包含能够增强非病毒基因表达的序列。对重复序列末端及其周围序列的检查表明,这些重复序列并非通过同源重组产生,并且没有迹象表明存在序列特异性机制导致它们的形成。然而,不同多瘤病毒毒株之间重复序列结构上的差异表明,这些序列重复是近期进化过程中出现的现象。本文讨论了这种变异潜在的生物学意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cd1/255237/bbac0a411a4c/jvirol00142-0242-a.jpg

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