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Comments on Benner LK et al. (2019) G3 (Bethesda) "The mir-35 Family Links Maternal Germline Sex to Embryonic Viability in Caenorhabditis elegans." (0)
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Benner LK, Prothro KP, & McJunkin K (2019). The mir-35 Family Links Maternal Germline Sex to Embryonic Viability in Caenorhabditis elegans. G3 (Bethesda), 9, 901-909. doi:10.1534/g3.118.200863
The germline sex determination pathway in <i>C. elegans</i> determines whether germ cells develop as oocytes or sperm, with no previously known effect on viability. The <i>mir-35</i> family of microRNAs are expressed in the <i>C. elegans</i> germline and embryo and are essential for both viability and normal hermaphroditic sex determination, preventing aberrant male gene expression in XX hermaphrodite embryos. Here we show that combining feminizing mutations with partial loss of function of the <i>mir-35</i> family results in enhanced penetrance embryonic lethality that preferentially kills XO animals. This lethal phenotype is due to altered signaling through the germline sex determination pathway, and maternal germline feminization is sufficient to induce enhanced lethality. These findings reveal a surprising pleiotropy of sperm-fate promoting pathways on organismal viability. Overall, our results demonstrate an unexpectedly strong link between sex determination and embryonic viability, and suggest that in wild type animals, <i>mir-35</i> family members buffer against misregulation of pathways outside the sex determination program, allowing for clean sex reversal rather than deleterious effects of perturbing sex determination genes.
