Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway;
Section for Cancer Cytogenetics, Institute for Cancer Genetics and Informatics, The Norwegian Radium Hospital, Oslo University Hospital, Oslo, Norway.
Cancer Genomics Proteomics. 2022 Nov-Dec;19(6):647-672. doi: 10.21873/cgp.20349.
Chromosomal translocations in cancer as well as benign neoplasias typically lead to the formation of fusion genes. Such genes may encode chimeric proteins when two protein-coding regions fuse in-frame, or they may result in deregulation of genes via promoter swapping or translocation of the gene into the vicinity of a highly active regulatory element. A less studied consequence of chromosomal translocations is the fusion of two breakpoint genes resulting in an out-of-frame chimera. The breaks then occur in one or both protein-coding regions forming a stop codon in the chimeric transcript shortly after the fusion point. Though the latter genetic events and mechanisms at first awoke little research interest, careful investigations have established them as neither rare nor inconsequential. In the present work, we review and discuss the truncation of genes in neoplastic cells resulting from chromosomal rearrangements, especially from seemingly balanced translocations.
染色体易位在癌症以及良性肿瘤中通常会导致融合基因的形成。当两个编码蛋白质的区域融合成框时,这些基因可能会编码嵌合蛋白,或者通过启动子交换或基因易位到高度活跃的调节元件附近,导致基因失活。染色体易位较少研究的后果是两个断点基因融合导致无框嵌合体。然后,在融合点后不久,在一个或两个蛋白质编码区中发生断裂,在嵌合转录本中形成一个终止密码子。尽管这些遗传事件和机制最初并没有引起太多的研究兴趣,但仔细的研究已经证实它们既不罕见也不无足轻重。在本工作中,我们综述和讨论了染色体重排,特别是看似平衡易位导致的肿瘤细胞中基因的截断。