| Literature DB >> 31361039 |
Taisuke Kajino1,2, Teppei Shimamura3, Shuyi Gong1, Kiyoshi Yanagisawa1, Lisa Ida1, Masahiro Nakatochi4, Sebastian Griesing1, Yukako Shimada1,2, Keiko Kano1, Motoshi Suzuki1, Satoru Miyano5, Takashi Takahashi1,6.
Abstract
Long non-coding RNAs (lncRNAs) function in a wide range of processes by diverse mechanisms, though their roles in regulation of oncogenes and/or tumor suppressors remain rather elusive. We performed a global search for lncRNAs affecting MYC activity using a systems biology-based approach with a K supercomputer and the GIMLET algorism based on local distance correlations. Consequently, MYMLR was identified and experimentally shown to maintain MYC transcriptional activity and cell cycle progression despite the low levels of expression. A proteomic search for MYMLR-binding proteins identified PCBP2, while it was also found that MYMLR places a 557-kb upstream enhancer region in the proximity of the MYC promoter in cooperation with PCBP2. These findings implicate a crucial role for MYMLR in regulation of the archetypical oncogene MYC and warrant future studies regarding the involvement of low copy number lncRNAs in regulation of other crucial oncogenes and tumor suppressor genes.Entities:
Keywords: zzm321990MYCzzm321990; enhancer; lncRNA; lung cancer; systems biology
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Year: 2019 PMID: 31361039 PMCID: PMC6717891 DOI: 10.15252/embj.201798441
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598