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Spontaneous and double-strand break-induced recombination, and gene conversion tract lengths, are differentially affected by overexpression of wild-type or ATPase-defective yeast Rad54

机译:野生型或ATPase缺陷型酵母Rad54的过表达对自发性和双链断裂诱导的重组以及基因转化道长度有不同的影响

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摘要

Rad54 plays key roles in homologous recombination (HR) and double-strand break (DSB) repair in yeast, along with Rad51, Rad52, Rad55 and Rad57. Rad54 belongs to the Swi2/Snf2 family of DNA-stimulated ATPases. Rad51 nucleoprotein filaments catalyze DNA strand exchange and Rad54 augments this activity of Rad51. Mutations in the Rad54 ATPase domain (ATPase–) impair Rad54 function in vitro, sensitize yeast to killing by methylmethane sulfonate and reduce spontaneous gene conversion. We found that overexpression of ATPase– Rad54 reduced spontaneous direct repeat gene conversion and increased both spontaneous direct repeat deletion and spontaneous allelic conversion. Overexpression of ATPase– Rad54 decreased DSB-induced allelic conversion, but increased chromosome loss and DSB-dependent lethality. Thus, ATP hydrolysis by Rad54 contributes to genome stability by promoting high-fidelity DSB repair and suppressing spontaneous deletions. Overexpression of wild-type Rad54 did not alter DSB-induced HR levels, but conversion tract lengths were reduced. Interestingly, ATPase– Rad54 decreased overall HR levels and increased tract lengths. These tract length changes provide new in vivo evidence that Rad54 functions in the post-synaptic phase during recombinational repair of DSBs.
机译:Rad54与Rad51,Rad52,Rad55和Rad57一起在酵母的同源重组(HR)和双链断裂(DSB)修复中起关键作用。 Rad54属于Swi2 / Snf2 DNA刺激的ATPase家族。 Rad51核蛋白细丝催化DNA链交换,Rad54增强Rad51的这种活性。 Rad54 ATPase结构域(ATPase–)中的突变会在体外损害Rad54的功能,使酵母菌对甲基磺酸甲酯的杀伤敏感,并减少自发基因转换。我们发现,ATPase–Rad54的过表达减少了自发直接重复序列基因的转化,同时增加了自发直接重复序列缺失和自发等位基因的转化。 ATPase–Rad54的过表达降低了DSB诱导的等位基因转化,但增加了染色体丢失和DSB依赖性致死率。因此,Rad54的ATP水解通过促进高保真DSB修复和抑制自发缺失而有助于基因组稳定性。野生型Rad54的过表达并没有改变DSB诱导的HR水平,但减少了转换道的长度。有趣的是,ATPase–Rad54降低了整体HR水平,并增加了呼吸道长度。这些束长度的变化提供了新的体内证据,表明在重组DSB的修复过程中Rad54在突触后阶段起作用。

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