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T4核酸内切酶V在合成DNA底物上引发的修复合成的体外特性研究。

In vitro characterization of repair synthesis initiated by T4 endonuclease V on a synthetic DNA substrate.

作者信息

Sancar A

机构信息

Department of Biochemistry and Biophysics, University of North Carolina, School of Medicine, Chapel Hill 27599.

出版信息

Indian J Biochem Biophys. 1992 Jun;29(3):227-30.

PMID:1512008
Abstract

The size of the repair patch produced by E. coli DNA polymerase (Pol I) following the removal of a pyrimidine dimer from DNA in response to the nicking activity of T4 endonuclease (T4 endo V) was determined. A 48-bp DNA containing a pyrimidine dimer at a defined location was labelled in the damaged strand and incubated with T4 endo V and E. coli endonuclease IV. Subsequently, DNA synthesis by DNA Pol I was carried out in the presence of four dNTPs, ATP and DNA ligase. Analysis of the reaction products on a sequencing gel revealed a ladder of only 4-oligonucleotides, 1-4 nucleotides greater in length than the fragment generated by the combined nicking activities of T4 endo V and E. coli endonuclease IV. Thus we conclude that the in vitro repair patch size of T4 endo V is 4 nucleotides and that in some cases the repaired DNA is not ligated.

摘要

测定了大肠杆菌DNA聚合酶(Pol I)在响应T4内切核酸酶(T4 endo V)的切口活性从DNA中去除嘧啶二聚体后产生的修复补丁的大小。在受损链中标记了一个在特定位置含有嘧啶二聚体的48bp DNA,并与T4 endo V和大肠杆菌内切核酸酶IV一起孵育。随后,在四种dNTP、ATP和DNA连接酶存在的情况下由DNA Pol I进行DNA合成。在测序凝胶上对反应产物的分析揭示了一个仅由4个寡核苷酸组成的梯状条带,其长度比由T4 endo V和大肠杆菌内切核酸酶IV的联合切口活性产生的片段长1-4个核苷酸。因此我们得出结论,T4 endo V的体外修复补丁大小为4个核苷酸,并且在某些情况下修复后的DNA未被连接。

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