Miao Lixia, Cao Zhijian, Shen Chao, Gu Meijia, Liu Wanhong, Li Hua, Zheng Congyi
State Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan, 430072, PR China.
Biochemistry (Mosc). 2008 Nov;73(11):1214-23. doi: 10.1134/s0006297908110072.
BRCA1 is an important tumor suppressor gene associated with inherited breast and ovarian cancers. In this investigation, two novel BRCA1 splicing variants were cloned from breast cancer cell line ZR-75-30. These transcripts, named BRCA1-PI21-Delta2-21 and BRCA1-Delta2-14, lacked most exons of full length BRCA1 gene, but maintained the original reading frame. We also demonstrated the presence of BRCA1-PI21-Delta2-21 in several human cell lines. Expression of both variants fused with green fluorescent protein (GFP) showed that they targeted different subcellular compartments in the transfected cells. Viability of the cells expressing both fusion proteins decreased notably compared with the viability of cells expressing only GFP. Fluorescence activated cell sorting assay confirmed that the overexpression of two splicing variants resulted in cell apoptosis. Taken together, the different subcellular localization and cell effects of two BRCA1 splicing variants imply that they can have different biological functions in breast cancer cells. Elucidating the functions of BRCA1 splicing variants would help to understand the exact roles of the BRCA1 gene in tumor suppression.
BRCA1是一种与遗传性乳腺癌和卵巢癌相关的重要肿瘤抑制基因。在本研究中,从乳腺癌细胞系ZR-75-30中克隆出两种新的BRCA1剪接变体。这些转录本分别命名为BRCA1-PI21-Delta2-21和BRCA1-Delta2-14,缺少全长BRCA1基因的大部分外显子,但保持了原来的阅读框。我们还在几种人类细胞系中证实了BRCA1-PI21-Delta2-21的存在。两种变体与绿色荧光蛋白(GFP)融合后的表达表明,它们在转染细胞中靶向不同的亚细胞区室。与仅表达GFP的细胞活力相比,表达两种融合蛋白的细胞活力显著降低。荧光激活细胞分选分析证实,两种剪接变体的过表达导致细胞凋亡。综上所述,两种BRCA1剪接变体不同的亚细胞定位和细胞效应表明它们在乳腺癌细胞中可能具有不同的生物学功能。阐明BRCA1剪接变体的功能将有助于了解BRCA1基因在肿瘤抑制中的确切作用。