| Literature DB >> 35234908 |
Michael B Davis1, Eshna Jash1, Bahaar Chawla1, Rebecca A Haines1, Lillian E Tushman1, Ryan Troll1, Györgyi Csankovszki1.
Abstract
Dosage compensation involves chromosome-wide gene regulatory mechanisms which impact higher order chromatin structure and are crucial for organismal health. Using a genetic approach, we identified Argonaute genes which promote dosage compensation in Caenorhabditis elegans. Dosage compensation in C. elegans hermaphrodites is initiated by the silencing of xol-1 and subsequent activation of the dosage compensation complex which binds to both hermaphrodite X chromosomes and reduces transcriptional output by half. A hallmark phenotype of dosage compensation mutants is decondensation of the X chromosomes. We characterized this phenotype in Argonaute mutants using X chromosome paint probes and fluorescence microscopy. We found that while nuclear Argonaute mutants hrde-1 and nrde-3, as well as mutants for the piRNA Argonaute prg-1, exhibit derepression of xol-1 transcripts, they also affect X chromosome condensation in a xol-1-independent manner. We also characterized the physiological contribution of Argonaute genes to dosage compensation using genetic assays and found that hrde-1 and nrde-3 contribute to healthy dosage compensation both upstream and downstream of xol-1.Entities:
Keywords: zzm321990 Caenorhabditis eleganszzm321990 ; Argonautes; FISH; X-linked gene expression; chromatin structure: gene regulation; development; dosage compensation; nuclear RNAi
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Year: 2022 PMID: 35234908 PMCID: PMC9071528 DOI: 10.1093/genetics/iyac033
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.402