| Literature DB >> 33372658 |
Behnom Farboud1,2, Catherine S Novak1,2, Monique Nicoll1,2, Alyssa Quiogue1,2, Barbara J Meyer1,2.
Abstract
We demonstrate how RNA binding protein FOX-1 functions as a dose-dependent X-signal element to communicate X-chromosome number and thereby determine nematode sex. FOX-1, an RNA recognition motif protein, triggers hermaphrodite development in XX embryos by causing non-productive alternative pre-mRNA splicing of xol-1, the master sex-determination switch gene that triggers male development in XO embryos. RNA binding experiments together with genome editing demonstrate that FOX-1 binds to multiple GCAUG and GCACG motifs in a xol-1 intron, causing intron retention or partial exon deletion, thereby eliminating male-determining XOL-1 protein. Transforming all motifs to GCAUG or GCACG permits accurate alternative splicing, demonstrating efficacy of both motifs. Mutating subsets of both motifs partially alleviates non-productive splicing. Mutating all motifs blocks it, as does transforming them to low-affinity GCUUG motifs. Combining multiple high-affinity binding sites with the twofold change in FOX-1 concentration between XX and XO embryos achieves dose-sensitivity in splicing regulation to determine sex.Entities:
Keywords: C. elegans; FOX-1 RNA binding protein; X-chromosome dose; X-signal element; alternative pre-mRNA splicing; chromosomes; dosage compensation; gene expression; sex determination signal
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Year: 2020 PMID: 33372658 PMCID: PMC7787662 DOI: 10.7554/eLife.62963
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140