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DNA双链断裂修复缺陷的哺乳动物细胞突变体中的V(D)J重组。

V(D)J recombination in mammalian cell mutants defective in DNA double-strand break repair.

作者信息

Pergola F, Zdzienicka M Z, Lieber M R

机构信息

Department of Pathology, Stanford University School of Medicine, California 94305-5324.

出版信息

Mol Cell Biol. 1993 Jun;13(6):3464-71. doi: 10.1128/mcb.13.6.3464-3471.1993.

Abstract

V(D)J recombination has been examined in several X-ray-sensitive and double-strand break repair-deficient Chinese hamster cell mutants. Signal joint formation was affected in four mutants (xrs 5, XR-1, V-3, and XR-V9B cells, representing complementation groups 1 through 4, respectively) defective in DNA double-strand break rejoining. Among these four, V-3 and XR-V9B were the most severely affected. Only in V-3 was coding joint formation also affected. Ataxia telangiectasia-like hamster cell mutants (V-E5 and V-G8), which are normal for double-strand break repair but are X ray sensitive, were normal for all aspects of the V(D)J recombination reaction, indicating that X-ray sensitivity is not the common denominator but that the deficiency in double-strand break repair appears to be. The abnormality at the signal joints consisted of an elevated incidence of nucleotide loss from each of the two signal ends. Interestingly, in complementation groups 1 (xrs 5) and 2 (XR-1), signal joint formation was within the normal range under some transfection conditions. This suggests that the affected gene products in these two complementation groups are not catalytic components. Instead, they may be either secondary or stochiometric components involved in the later stages of both the V(D)J recombination reaction and double-strand break repair. The fact that such factors can affect the precision of the signal joint has mechanistic implications for V(D)J recombination.

摘要

已在几种对X射线敏感且双链断裂修复缺陷的中国仓鼠细胞突变体中研究了V(D)J重组。在四个DNA双链断裂重新连接有缺陷的突变体(xrs 5、XR-1、V-3和XR-V9B细胞,分别代表互补组1至4)中,信号接头形成受到影响。在这四个突变体中,V-3和XR-V9B受影响最严重。只有在V-3中,编码接头形成也受到影响。共济失调毛细血管扩张样仓鼠细胞突变体(V-E5和V-G8),其双链断裂修复正常但对X射线敏感,在V(D)J重组反应的所有方面均正常,这表明X射线敏感性不是共同特征,而双链断裂修复缺陷似乎是。信号接头处的异常包括两个信号末端各自核苷酸丢失的发生率升高。有趣的是,在互补组1(xrs 5)和2(XR-1)中,在某些转染条件下信号接头形成在正常范围内。这表明这两个互补组中受影响的基因产物不是催化成分。相反,它们可能是参与V(D)J重组反应和双链断裂修复后期的次要成分或化学计量成分。这种因素会影响信号接头精度这一事实对V(D)J重组具有机制上的意义。

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