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5-甲酰尿嘧啶的酶促修复。II. DNA复制过程中5-甲酰尿嘧啶与鸟嘌呤之间错配的形成及其被参与碱基切除修复(AlkA)和错配修复(MutS)的两种蛋白质识别。

Enzymatic repair of 5-formyluracil. II. Mismatch formation between 5-formyluracil and guanine during dna replication and its recognition by two proteins involved in base excision repair (AlkA) and mismatch repair (MutS).

作者信息

Terato H, Masaoka A, Kobayashi M, Fukushima S, Ohyama Y, Yoshida M, Ide H

机构信息

Graduate Department of Gene Science, Faculty of Science, Hiroshima University, Kagamiyama, Higashi-Hiroshima 739-8526, Japan.

出版信息

J Biol Chem. 1999 Aug 27;274(35):25144-50. doi: 10.1074/jbc.274.35.25144.

Abstract

5-Formyluracil (fU), a major methyl oxidation product of thymine, forms correct (fU:A) and incorrect (fU:G) base pairs during DNA replication. In the accompanying paper (Masaoka, A., Terato, H., Kobayashi, M., Honsho, A., Ohyama, Y., and Ide, H. (1999) J. Biol. Chem. 274, 25136-25143), it has been shown that fU correctly paired with A is recognized by AlkA protein (Escherichia coli 3-methyladenine DNA glycosylase II). In the present work, mispairing frequency of fU with G and cellular repair protein that specifically recognized fU:G mispairs were studied using defined oligonucleotide substrates. Mispairing frequency of fU was determined by incorporation of 2'-deoxyribonucleoside 5'-triphosphate of fU opposite template G using DNA polymerase I Klenow fragment deficient in 3'-5' exonuclease. Mispairing frequency of fU was dependent on the nearest neighbor base pair in the primer terminus and 2-12 times higher than that of thymine at pH 7.8 and 2.6-6.7 times higher at pH 9.0 with an exception of the nearest neighbor T(template):A(primer). AlkA catalyzed the excision of fU placed opposite G, as well as A, and the excision efficiencies of fU for fU:G and fU:A pairs were comparable. In addition, MutS protein involved in methyl-directed mismatch repair also recognized fU:G mispairs and bound them with an efficiency comparable to T:G mispairs, but it did not recognize fU:A pairs. Prior complex formation between MutS and a heteroduplex containing an fU:G mispair inhibited the activity of AlkA to fU. These results suggest that fU present in DNA can be restored by two independent repair pathways, i.e. the base excision repair pathway initiated by AlkA and the methyl-directed mismatch repair pathway initiated by MutS. Biological relevance of the present results is discussed in light of DNA replication and repair in cells.

摘要

5-甲酰尿嘧啶(fU)是胸腺嘧啶的主要甲基氧化产物,在DNA复制过程中会形成正确的(fU:A)和错误的(fU:G)碱基对。在随附的论文中(正冈,A.,寺户,H.,小林,M.,本庄,A.,大山,Y.,和井手,H.(1999年)《生物化学杂志》274,25136 - 25143),已经表明与A正确配对的fU可被AlkA蛋白(大肠杆菌3-甲基腺嘌呤DNA糖基化酶II)识别。在本研究中,使用确定的寡核苷酸底物研究了fU与G的错配频率以及特异性识别fU:G错配的细胞修复蛋白。fU的错配频率是通过使用缺乏3'-5'外切核酸酶的DNA聚合酶I Klenow片段将fU的2'-脱氧核糖核苷5'-三磷酸掺入与模板G相对的位置来确定的。fU的错配频率取决于引物末端的相邻碱基对,在pH 7.8时比胸腺嘧啶高2 - 12倍,在pH 9.0时高2.6 - 6.7倍,但与相邻的T(模板):A(引物)情况不同。AlkA催化切除与G以及A相对的fU,并且fU对于fU:G和fU:A对的切除效率相当。此外,参与甲基导向错配修复的MutS蛋白也识别fU:G错配并以与T:G错配相当的效率结合它们,但它不识别fU:A对。MutS与含有fU:G错配的异源双链体之间预先形成复合物会抑制AlkA对fU的活性。这些结果表明DNA中存在的fU可通过两条独立的修复途径恢复,即由AlkA启动的碱基切除修复途径和由MutS启动的甲基导向错配修复途径。根据细胞中的DNA复制和修复对本研究结果的生物学意义进行了讨论。

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