Tunable Transcriptional Interference at the Endogenous Alcohol Dehydrogenase Gene Locus in Drosophila melanogaster
Year: 2020
Type: article
Abstract: Neighboring sequences of a gene can influence its expression. In the phenomenon known as transcriptional interference, transcription at one region in the genome can repress transcription at a nearby region in cis. Transcriptional interference occurs at a number of eukaryotic loci, including the alcohol dehydrogenase (Adh) gene in Drosophila melanogaster. Adh is regulated by two promoters, which are distinct in their developmental timing of activation. It has been shown using transgene insertion that when the promoter distal from the Adh start codon is deleted, transcription from the proximal promoter becomes de-regulated. As a result, the Adh proximal promoter, which is normally active only during the early larval stages, becomes abnormally activated in adults. Whether this type of regulation occurs in the endogenous Adh context, however, remains unclear. Here, we employed the CRISPR/Cas9 system to edit the endogenous Adh locus and found that removal of the distal promoter also resulted in the untimely expression of the proximal promoter-driven mRNA isoform in adults, albeit at lower levels than previously reported. Importantly, transcription from the distal promoter was sufficient to repress proximal transcription in larvae, and the degree of this repression was dependent on the degree of distal promoter activity. Finally, upregulation of the distal Adh transcript led to the enrichment of histone 3 lysine 36 trimethylation over the Adh proximal promoter. We conclude that the endogenous Adh locus is developmentally regulated by transcriptional interference in a tunable manner.
Source: G3 Genes Genomes Genetics
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,709
Funders: National Science Foundation, Pew Charitable Trusts, Alfred P. Sloan Foundation, Damon Runyon Cancer Research Foundation, Glenn Foundation for Medical Research, University of California Berkeley, Shurl and Kay Curci Foundation, Fondation pour la Recherche Médicale, National Institutes of Health, National Institute on Aging, National Institute of General Medical Sciences, National Center for Research Resources
Awards: G1637196319, G1751806681, G1823892030, G2271678686, Graduate Research Fellowship Program, Graduate Research Fellowship Program (GRFP), ILLUMINATING CELLULAR AGING PATHWAYS THROUGH GAMETOGENESIS, G3323069144, G5068202634, G5113983396, G6212112174, G8420061266, LTQ XL Linear Quadrupole Ion Trap Mass Spectrometer, Dissecting the roles of pervasive short ORFs in meiosis
OpenAlex ID: W3013863362
