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在粗糙脉孢菌中从het - c异核体不相容性中逃逸的分离株中的染色体重排。

Chromosome rearrangements in isolates that escape from het-c heterokaryon incompatibility in Neurospora crassa.

作者信息

Xiang Qijun, Glass N Louise

机构信息

Department of Plant and Microbial Biology, University of California, Berkeley, CA 94720-3102, USA.

出版信息

Curr Genet. 2004 Jan;44(6):329-38. doi: 10.1007/s00294-003-0451-y. Epub 2003 Oct 17.

DOI:10.1007/s00294-003-0451-y
PMID:14564476
Abstract

Chromosomal rearrangement is implicated in human cancers and hereditary diseases. Mechanisms generating chromosomal rearrangements may be shared by a variety of organisms. Spontaneous chromosomal rearrangements, especially large deletions, take place at high frequency in isolates that escape from heterokaryon incompatibility in Neurospora crassa. In this study, chromosomal rearrangements were detected in strains that had escaped from het-c heterokaryon incompatibility in N. crassa. A vc1 mutant carried a 20-kbp deletion covering five ORFs. A vc2 mutant carried a complex chromosome rearrangement with an 8-kbp deletion covering three ORFs, a 34-bp deletion and an 80-kbp inversion. The break-points of chromosome rearrangements in the vc1 and vc2 mutants all have direct repeats of 2 bp, similar to the break-points of some chromosome rearrangements associated with human cancer and genetic diseases. An ahc mutant carried a 31-kbp deletion covering at least 11 ORFs and a het-c deletion mutant carried a 7-kbp deletion covering two ORFs. Additional chromosomal rearrangements occurred in these two strains. These results indicate that escape from heterokaryon incompatibility can be used as a model system for chromosome rearrangement and DNA-repair studies. The impact of the chromosomal rearrangements is discussed, especially the deletion of the predicted ORFs on the phenotype of mutants.

摘要

染色体重排与人类癌症和遗传性疾病有关。产生染色体重排的机制可能在多种生物体中是共有的。自发染色体重排,尤其是大的缺失,在粗糙脉孢菌中逃避异核体不相容性的分离株中高频发生。在本研究中,在粗糙脉孢菌中逃避het-c异核体不相容性的菌株中检测到染色体重排。一个vc1突变体携带一个20-kbp的缺失,覆盖五个开放阅读框。一个vc2突变体携带一个复杂的染色体重排,有一个8-kbp的缺失覆盖三个开放阅读框、一个34-bp的缺失和一个80-kbp的倒位。vc1和vc2突变体中染色体重排的断点都有2 bp的直接重复序列,类似于一些与人类癌症和遗传疾病相关的染色体重排的断点。一个ahc突变体携带一个31-kbp的缺失,覆盖至少11个开放阅读框,一个het-c缺失突变体携带一个7-kbp的缺失,覆盖两个开放阅读框。这两个菌株中还发生了其他染色体重排。这些结果表明,逃避异核体不相容性可以用作染色体重排和DNA修复研究的模型系统。讨论了染色体重排的影响,特别是预测的开放阅读框的缺失对突变体表型的影响。

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