The QxxR Motif of RNA Helicase Me31B Is Essential for Drosophila Female Fertility and Germline Development
Mansoor, R.; Minhas, A. S.; Thomas, A.; Mansoor, A. A.; McCambridge, A. H.; Dilts, C.; Eshak, J.; Govani, D.; Nylin, B.; Trinidad, J. C.; Kanaan, A. Y.; Kara, E.; Fielder, A.; Fielder, I.; Iglendza, A.; Mukatash, Y.; Pumnea, B.; Menzel, M. M.; Shabazz-Henry, A. L.; Niepielko, M. G.; Gao, M.
Show abstract
The QxxR motif is evolutionarily conserved within DEAD-box RNA helicases, including Drosophila Me31B and human DDX6, which post-transcriptionally regulate gene expression during animal development. A pathogenic H372R substitution (QxHR to QxRR) in the QxxR motif of human DDX6 has been associated with various developmental defects, but how this motif contributes to DDX6-family protein function remains unclear. Here, we used Drosophila Me31B as an in vivo model to investigate the QxxR motifs developmental role. We generated a Drosophila strain carrying the corresponding H333R missense mutation in Me31B and characterized its effects on female fertility, embryonic viability, germline development, and Me31B-associated molecular pathways. The me31BH333R mutation reduced female fertility in a gene dose-dependent manner, with homozygous mutant females being sterile. Embryos from the mutant females also exhibited primordial germ cell defects. Despite these developmental phenotypes, the me31BH333R mutation did not significantly alter Me31B protein abundance, global ovarian transcriptome or proteome profiles, or representative germ plasm mRNA and protein localization. In contrast, bait-normalized IP-MS analysis revealed altered enrichment of selected Me31B-associated proteins, including increased association of known Me31B interactors Trailer hitch (Tral) and Ypsilon Schachtel (Yps). These findings establish Me31BH333R as an in vivo model for investigating the conserved QxxR motif and suggest that disruption of this motif compromises development not through broad changes in gene expression, but potentially through altered composition or regulation of Me31B-containing ribonucleoprotein complexes.
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