| Literature DB >> 33290723 |
Xiang Yu1, Matthew R Willmann2, Lee E Vandivier3, Sophie Trefely4, Marianne C Kramer3, Jeffrey Shapiro1, Rong Guo1, Eric Lyons5, Nathaniel W Snyder6, Brian D Gregory7.
Abstract
Although eukaryotic messenger RNAs (mRNAs) normally possess a 5' end N7-methyl guanosine (m7G) cap, a non-canonical 5' nicotinamide adenine dinucleotide (NAD+) cap can tag certain transcripts for degradation mediated by the NAD+ decapping enzyme DXO1. Despite this importance, whether NAD+ capping dynamically responds to specific stimuli to regulate eukaryotic transcriptomes remains unknown. Here, we reveal a link between NAD+ capping and tissue- and hormone response-specific mRNA stability. In the absence of DXO1 function, transcripts displaying a high proportion of NAD+ capping are instead processed into RNA-dependent RNA polymerase 6-dependent small RNAs, resulting in their continued turnover likely to free the NAD+ molecules. Additionally, the NAD+-capped transcriptome is significantly remodeled in response to the essential plant hormone abscisic acid in a mechanism that is primarily independent of DXO1. Overall, our findings reveal a previously uncharacterized and essential role of NAD+ capping in dynamically regulating transcript stability during specific physiological responses.Entities:
Keywords: ABA; NAD capping; RNA degradation; RNA modification; RNA stability; abscisic acid; epitranscriptome; post-transcriptional regulation
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Year: 2020 PMID: 33290723 PMCID: PMC8934595 DOI: 10.1016/j.devcel.2020.11.009
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270