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腺相关病毒DNA的多种结构:用核酸内切酶R-Hae III对末端标记分子的分析

Multiple structures of adeno-associated virus DNA: analysis of terminally labeled molecules with endonuclease R-Hae III.

作者信息

Denhardt D T, Eisenberg S, Bartok K, Carter B J

出版信息

J Virol. 1976 May;18(2):672-84. doi: 10.1128/JVI.18.2.672-684.1976.

Abstract

The double-stranded form of adeno-associated virus (AAV) DNA has about 20 sites sensitive to endonuclease R.Hae III from Haemophilus aegypitus; the fragments produced fall into about 13 size classes, 8 of which contain single fragments. The location of the Hae III-produced AAV fragments relative to the three EcoR1 fragments was determined. Using revised figures for the molecular weights of the Hae III cleavage products of phiX174 replicative form DNA, we calculated that AAV DNA contains about 4,000 nucleotides. After Hae III digestiion of duplex DNA terminally labeled with 32P using polynucleotide kinase, the majority of fragments containing a 5' 32P label were about 40 nucleotides in length, and fragments of similar size were generated from each end, suggesting that the Hae site closest to the end is within the terminal repetition. Two more-slowly-migrating cleavage products also bore 5' 32P end label. These three terminally labeled species were also generated from single-stranded AAV DNA by digestion with Hae III, and evidence that one may have a nonlinear ("rabbit-ear") structure is presented. The predominant 5' terminal base was identified as thymine for both the plus and minus strands of AAV. Single-stranded AAV molecules could not be efficiently covalently circularized by incubation with polynucleotide ligase or ligase plus T4 DNA polymerase.

摘要

腺相关病毒(AAV)DNA的双链形式有大约20个对来自埃及嗜血杆菌的核酸内切酶R.Hae III敏感的位点;产生的片段分为大约13个大小类别,其中8个含有单个片段。确定了由Hae III产生的AAV片段相对于三个EcoR1片段的位置。使用经修订的φX174复制型DNA的Hae III切割产物的分子量数据,我们计算出AAV DNA含有约4000个核苷酸。在用多核苷酸激酶对用32P末端标记的双链DNA进行Hae III消化后,大多数含有5' 32P标记的片段长度约为40个核苷酸,并且从两端产生了大小相似的片段,这表明最靠近末端的Hae位点在末端重复序列内。另外两个迁移较慢的切割产物也带有5' 32P末端标记。通过用Hae III消化单链AAV DNA也产生了这三种末端标记的产物,并且提供了其中一种可能具有非线性(“兔耳”)结构的证据。确定AAV正链和负链的主要5'末端碱基均为胸腺嘧啶。单链AAV分子不能通过与多核苷酸连接酶或连接酶加T4 DNA聚合酶一起温育而有效地共价环化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc84/515595/765062ce4493/jvirol00221-0324-a.jpg

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