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Trombley, N. J.

Publications and source records attributed to Trombley, N. J..

2 recordsLinked to original sources

Targeted RNAi screen reveals novel regulators of RNA-binding protein phase transitions in Caenorhabditis elegans oocytes

The ability of oocytes to maintain their quality is essential for successful reproduction. One critical aspect of oocyte quality and successful embryogenesis after fertilization is the proper regulation of the stores of maternal mRNA by RNA-binding proteins. Many RNA-binding proteins undergo regulated phase transitions during oogenesis, and alterations of the protein phase can disrupt its ability to regulate mRNA stability and translation. In C. elegans, genetic screens have identified regulators of RNA-binding protein condensation in arrested oocytes of females and in embryos, but less attention has focused on phase transitions in maturing oocytes of young adult hermaphrodites. Interestingly, of the relatively few regulators of RNA-binding protein phase transitions identified to date in maturing oocytes, several genes overlap with those required for clearance of protein aggregates in maturing oocytes. To determine the extent to which the temporally linked processes of clearance of damaged proteins and maintenance of RNP complexes are coordinated at a molecular level, we conducted a targeted RNAi screen of genes required for removal of protein aggregates in maturing oocytes. We identified six novel regulators of phase transitions of the KH-domain protein MEX-3 and obtained strong evidence that the regulatory network of protein aggregate clearance overlaps with, but is distinct from, the regulation of MEX-3 phase transitions in the oocyte.

genetics↗

The CCT chaperonin and actin modulate the ER and RNA-binding protein condensation during oogenesis to maintain translational repression of maternal mRNA and oocyte quality

The regulation of maternal mRNAs is essential for proper oogenesis, the production of viable gametes, and to avoid birth defects and infertility. Many oogenic RNA-binding proteins have been identified with roles in mRNA metabolism, some of which localize to dynamic ribonucleoprotein granules and others that appear dispersed. Here, we use a combination of in vitro condensation assays and the in vivo C. elegans oogenesis model to determine the intrinsic properties of the conserved KH-domain MEX-3 protein and to identify novel regulators of MEX-3 and the Lsm protein, CAR-1. We demonstrate that MEX-3 undergoes liquid-liquid phase separation and appears to have intrinsic gel-like properties in vitro. We also identify novel roles for the CCT chaperonin and actin in preventing ectopic RNA-binding protein condensates in maturing oocytes that appear to be independent of MEX-3 folding. CCT and actin also oppose the expansion of ER sheets that may promote ectopic condensation of RNA-binding proteins that are associated with de-repression of maternal mRNA. This regulatory network is essential to preserve oocyte quality, prevent infertility, and may have implications for understanding the role of hMex3 phase transitions in cancer. Significance statementO_LIThe molecular mechanisms that regulate phase transitions of oogenic RNA-binding proteins are critical to elucidate but are not fully understood. C_LIO_LIWe identify novel regulators of RNA-binding protein phase transitions in maturing oocytes that are required to maintain translational repression of maternal mRNAs and oocyte quality. C_LIO_LIThis study is the first to elucidate a regulatory network involving the CCT chaperonin, actin, and the ER for phase transitions of RNA-binding proteins during oogenesis. Our findings for the conserved MEX-3 protein may also be applicable to better understanding the role of hMex3 phase transitions in cancer. C_LI

developmental biology↗