Isolation of cancer-specific chimeric transcripts induced by hypomethylation of the LINE-1 antisense promoter

被引:78
作者
Cruickshanks, Hazel A.
Tufarelli, Cristina [1 ]
机构
[1] Univ Nottingham, Wolfson Ctr Stem Cells Tissue Engn & Modelling, Ctr Biomol Sci, Nottingham NG7 2RD, England
关键词
Breast cancer; Chimeric transcripts; Colon cancer; Hypomethylation; LINE-1; Retrotransposon; CHRONIC MYELOID-LEUKEMIA; BETA-GLOBIN LOCUS; INTERGENIC TRANSCRIPTION; L1; RETROTRANSPOSITION; CYTOSINE METHYLATION; DNA HYPOMETHYLATION; GENETIC INSTABILITY; CELL-LINES; TUMORS; RNA;
D O I
10.1016/j.ygeno.2009.08.013
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The antisense promoter of human LINE-1 (L1) retroelements can direct transcription of adjacent unique genomic sequences generating chimeric RNAs, which can perturb transcription of neighbouring genes. As L1 elements constitute 17% of the human genome, chimeric transcription is potentially widespread, but the extent to which this Occurs is largely unknown. Using a genome-wide screen we have isolated novel chimeric transcripts that are unique to breast cancer cell lines, primary tumours and colon cancer cells. Expression of the cancer-specific chimeric transcripts can be induced in non-malignant breast epithelial cells by the demethylating drug 5-azacytidine. These findings indicate that loss of L1 methylation in cancer cells is linked to the expression of L1-chimeric transcripts which may therefore constitute a useful set of markers of malignancy. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:397 / 406
页数:10
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