4.8 Article

Divergent lncRNA MYMLR regulates MYC by eliciting DNA looping and promoter-enhancer interaction

Journal

EMBO JOURNAL
Volume 38, Issue 17, Pages -

Publisher

WILEY
DOI: 10.15252/embj.201798441

Keywords

enhancer; lncRNA; lung cancer; MYC; systems biology

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan [15H05910]
  2. Japan Society for the Promotion of Science [16H02468, 16K19050]
  3. Princess Takamatsu Cancer Research Fund
  4. Japan Agency for Medical Research and development (AMED) [18ck0106363h0002]
  5. Grants-in-Aid for Scientific Research [16K19050, 15H05910, 16H02468] Funding Source: KAKEN

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available