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Saccharomyces cerevisiae RAD5-encoded DNA repair protein contains DNA helicase and zinc-binding sequence motifs and affects the stability of simple repetitive sequences in the genome.

机译:啤酒酵母RAD5编码的DNA修复蛋白包含DNA解旋酶和锌结合序列基序并影响基因组中简单重复序列的稳定性。

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摘要

rad5 (rev2) mutants of Saccharomyces cerevisiae are sensitive to UV light and other DNA-damaging agents, and RAD5 is in the RAD6 epistasis group of DNA repair genes. To unambiguously define the function of RAD5, we have cloned the RAD5 gene, determined the effects of the rad5 deletion mutation on DNA repair, DNA damage-induced mutagenesis, and other cellular processes, and analyzed the sequence of RAD5-encoded protein. Our genetic studies indicate that RAD5 functions primarily with RAD18 in error-free postreplication repair. We also show that RAD5 affects the rate of instability of poly(GT) repeat sequences. Genomic poly(GT) sequences normally change length at a rate of about 10(-4); this rate is approximately 10-fold lower in the rad5 deletion mutant than in the corresponding isogenic wild-type strain. RAD5 encodes a protein of 1,169 amino acids of M(r) 134,000, and it contains several interesting sequence motifs. All seven conserved domains found associated with DNA helicases are present in RAD5. RAD5 also contains a cysteine-rich sequence motif that resembles the corresponding sequences found in 11 other proteins, including those encoded by the DNA repair gene RAD18 and the RAG1 gene required for immunoglobin gene arrangement. A leucine zipper motif preceded by a basic region is also present in RAD5. The cysteine-rich region may coordinate the binding of zinc; this region and the basic segment might constitute distinct DNA-binding domains in RAD5. Possible roles of RAD5 putative ATPase/DNA helicase activity in DNA repair and in the maintenance of wild-type rates of instability of simple repetitive sequences are discussed.
机译:酿酒酵母的rad5(rev2)突变体对紫外线和其他破坏DNA的物质敏感,而RAD5属于DNA修复基因的RAD6上位性组。为了明确定义RAD5的功能,我们克隆了RAD5基因,确定了rad5缺失突变对DNA修复,DNA损伤诱导的诱变和其他细胞过程的影响,并分析了RAD5编码蛋白的序列。我们的基因研究表明,RAD5在无错误的复制后修复中主要与RAD18一起起作用。我们还表明,RAD5影响poly(GT)重复序列的不稳定性速率。基因组poly(GT)序列通常以约10(-4)的速率改变长度;在rad5缺失突变体中,该比率比相应的同基因野生型菌株低约10倍。 RAD5编码M(r)134,000的1,169个氨基酸的蛋白质,并且包含几个有趣的序列基序。发现与DNA解旋酶相关的所有七个保守结构域都存在于RAD5中。 RAD5还包含一个富含半胱氨酸的序列基序,类似于在其他11种蛋白质中发现的相应序列,包括由DNA修复基因RAD18和免疫球蛋白基因排列所需的RAG1基因编码的蛋白质。在RAD5中还存在在基本区域之前的亮氨酸拉链基序。富含半胱氨酸的区域可以协调锌的结合;该区域和基本区段可能构成RAD5中不同的DNA结合结构域。讨论了RAD5假定的ATPase / DNA解旋酶活性在DNA修复和维持简单重复序列的野生型不稳定性速率中的可能作用。

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