MORC-1 is a key component of the C. elegans CSR-1 germline gene licensing mechanism

The Argonaute CSR-1 is essential for germline development in C. elegans . Mutation of csr-1 downregulates thousands of germline-expressed genes, leading to the model that the CSR-1-mediated small RNA pathway promotes, or “licenses,” gene expression by an unknown mechanism. CSR-1 also silences a limited number of genes through its canonical endonucleolytic “slicer” activity. We show that the GHKL-type ATPase MORC-1, a CSR-1 slicing target, over-accumulates at CSR-1 “licensed” target genes in csr-1 ( - ), which correlates with ectopic gain of H3K9me3, H3K36me3 loss, and gene downregulation. Loss of morc-1 rescues csr-1 ( - ) defects, while overexpressing MORC-1 in the germline of wild-type worms is sufficient to cause sterility and downregulate CSR-1 targets. These results show that MORC-1 overexpression in csr-1 ( - ) is a primary driver of the CSR-1-mediated gene licensing mechanism.