| Literature DB >> 35443176 |
Lauren Winkler1, Maria Jimenez1, Joshua T Zimmer2, Adam Williams3, Matthew D Simon2, Nadya Dimitrova4.
Abstract
The p53-induced long noncoding RNA (lncRNA) lincRNA-p21 is proposed to act in cis to promote p53-dependent expression of the neighboring cell cycle gene, Cdkn1a/p21. The molecular mechanism through which the transcribed lincRNA-p21 regulatory locus activates p21 expression remains poorly understood. To elucidate the functional elements of cis-regulation, we generate a series of genetic models that disrupt DNA regulatory elements, the transcription of lincRNA-p21, or the accumulation of mature lincRNA-p21. Unexpectedly, we determine that full-length transcription, splicing, and accumulation of lincRNA-p21 are dispensable for the chromatin organization of the locus and for cis-regulation. Instead, we find that production of lincRNA-p21 through conserved regions in exon 1 of lincRNA-p21 promotes cis-activation. These findings demonstrate that the activation of nascent transcription from this lncRNA locus, but not the generation or accumulation of a mature lncRNA transcript, is necessary to enact local gene expression control.Entities:
Keywords: CP: Molecular biology; cis-regulation; genetic models; lincRNA-p21; long noncoding RNA; transcription
Mesh:
Substances:
Year: 2022 PMID: 35443176 PMCID: PMC9118141 DOI: 10.1016/j.celrep.2022.110687
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423