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肺炎链球菌中的超重组:A/G到C.G修复及对DNA聚合酶I的需求

Hyperrecombination in pneumococcus: A/G to C.G repair and requirement for DNA polymerase I.

作者信息

Pasta F, Sicard M A

机构信息

Laboratoire de Microbiologie et Génétique cellulaire du C.N.R.S., Université Paul Sabatier, Toulouse, France.

出版信息

Mutat Res. 1994 Sep;315(2):113-22. doi: 10.1016/0921-8777(94)90012-4.

Abstract

During pneumococcal transformation, we had previously described that the ami36 mutation, which results from a C.G to A.T transversion, induces a large excess of wild-type recombinants in two point crosses. Upon donor-recipient DNA recombination, two heteroduplexes are generated by this mutation: A36/G+ and C+/T36. In two point crosses, hyperrecombination is observed only when transformation leads to the A/G mismatch. Here, we have studied the separate evolution of A36/G+ and C+/T36 heterozygotes created upon transformation of an ami36 mutant strain with artificial heteroduplex DNAs. We found that the A36/G+ mismatch leads to a preferential generation of wild-type progeny as compared with the complementary C+/T36 mismatch. This result suggests that A/G carrying transformants partly behave as wild-type homozygotes. The only way to account for such behavior is an excision repair correcting some A/G mispairs created upon transformation into C.G pairs. Moreover, we show that hyperrecombination triggered by ami36 is strongly reduced in a DNA polymerase I deficient strain. This strengthens the fact of DNA repair synthesis, which should be therefore prominently due to DNA polymerase I.

摘要

在肺炎球菌转化过程中,我们之前曾描述过,由C.G到A.T颠换导致的ami36突变,在两点杂交中会诱导产生大量过量的野生型重组体。在供体-受体DNA重组时,该突变会产生两个异源双链体:A36/G+和C+/T36。在两点杂交中,只有当转化导致A/G错配时才会观察到超重组。在此,我们研究了用人工异源双链DNA转化ami36突变株时产生的A36/G+和C+/T36杂合子的单独进化情况。我们发现,与互补的C+/T36错配相比,A36/G+错配会优先产生野生型后代。这一结果表明,携带A/G的转化体部分表现得如同野生型纯合子。解释这种行为的唯一方式是一种切除修复,它能将转化时产生的一些A/G错配校正为C.G对。此外,我们表明,在DNA聚合酶I缺陷型菌株中,ami36引发的超重组会大大减少。这强化了DNA修复合成这一事实,因此这应该主要归因于DNA聚合酶I。

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