Human colorectal cancer-specific CCAT1-L lncRNA regulates long-range chromatin interactions at the MYC locus

Jian‐Feng Xiang(Center for Excellence in Molecular Cell Science), Qing-Fei Yin(Center for Excellence in Molecular Cell Science), Tian Chen(Center for Excellence in Molecular Cell Science), Yang Zhang(Center for Excellence in Molecular Cell Science), Xiao‐Ou Zhang(Chinese Academy of Sciences), Zheng Wu(Center for Excellence in Molecular Cell Science), Shaofeng Zhang(Center for Excellence in Molecular Cell Science), Haibin Wang(Second Military Medical University), Junhui Ge(Second Military Medical University), Xuhua Lu(Second Military Medical University), Li Yang(Chinese Academy of Sciences), Ling‐Ling Chen(Center for Excellence in Molecular Cell Science)
Cell Research
March 25, 2014
Cited by 736Open Access
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Abstract

The human 8q24 gene desert contains multiple enhancers that form tissue-specific long-range chromatin loops with the MYC oncogene, but how chromatin looping at the MYC locus is regulated remains poorly understood. Here we demonstrate that a long noncoding RNA (lncRNA), CCAT1-L, is transcribed specifically in human colorectal cancers from a locus 515 kb upstream of MYC. This lncRNA plays a role in MYC transcriptional regulation and promotes long-range chromatin looping. Importantly, the CCAT1-L locus is located within a strong super-enhancer and is spatially close to MYC. Knockdown of CCAT1-L reduced long-range interactions between the MYC promoter and its enhancers. In addition, CCAT1-L interacts with CTCF and modulates chromatin conformation at these loop regions. These results reveal an important role of a previously unannotated lncRNA in gene regulation at the MYC locus.


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