Department of Biochemistry, Indian Institute of Science, Bangalore 560 012, India.
Nucleic Acids Res. 2011 Aug;39(14):5813-25. doi: 10.1093/nar/gkr223. Epub 2011 Apr 15.
Chromosomal translocations are one of the most common types of genetic rearrangements and are molecular signatures for many types of cancers. They are considered as primary causes for cancers, especially lymphoma and leukemia. Although many translocations have been reported in the last four decades, the mechanism by which chromosomes break during a translocation remains largely unknown. In this review, we summarize recent advances made in understanding the molecular mechanism of chromosomal translocations.
染色体易位是最常见的遗传重排类型之一,也是许多类型癌症的分子特征。它们被认为是癌症的主要原因,特别是淋巴瘤和白血病。尽管在过去四十年中已经报道了许多易位,但染色体在易位过程中发生断裂的机制在很大程度上仍不清楚。在这篇综述中,我们总结了在理解染色体易位的分子机制方面取得的最新进展。