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    Date Issued2018 (1)2015 (1)AuthorTu, Shikui (2)Weng, Zhiping (2)
    Wu, Monica Z. (2)
    Anderson, Joshua W. T. (1)Boag, Peter R. (1)View MoreUMass Chan AffiliationProgram in Bioinformatics and Integrative Biology (2)Document TypeJournal Article (1)Preprint (1)Keyword22G-RNA (1)Amino Acids, Peptides, and Proteins (1)Animals (1)Argonaute Proteins (1)Biochemistry (1)View MoreJournalbioRxiv (1)Nucleic acids research (1)

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    The TRIM-NHL protein NHL-2 is a Novel Co-Factor of the CSR-1 and HRDE-1 22G-RNA Pathways [preprint]

    Boag, Peter R.; Davis, Gregory M.; Tu, Shikui; Colson, Rhys N.; Anderson, Joshua W. T.; Gunzburg, Menachem J.; Francisco, Michelle A.; Ray, Debashish; Maity, Tuhin; Wu, Monica Z.; et al. (2018-02-05)
    Proper regulation of germline gene expression is essential for fertility and maintaining species integrity. In the C. elegans germline, a diverse repertoire of regulatory pathways promote the expression of endogenous germline genes and limit the expression of deleterious transcripts to maintain genome homeostasis. Here we show that the conserved TRIM-NHL protein, NHL-2, plays an essential role in the C. elegans germline, modulating germline chromatin and meiotic chromosome organization. We uncover a role for NHL-2 as a co-factor in both positively (CSR-1) and negatively (HRDE-1) acting germline 22G-small RNA pathways and the somatic nuclear RNAi pathway. Furthermore, we demonstrate that NHL-2 is a bona fide RNA binding protein and, along with RNA-seq data point to a small RNA independent role for NHL-2 in regulating transcripts at the level of RNA stability. Collectively, our data implicate NHL-2 as an essential hub of gene regulatory activity in both the germline and soma.
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    Comparative functional characterization of the CSR-1 22G-RNA pathway in Caenorhabditis nematodes

    Tu, Shikui; Wu, Monica Z.; Wang, Jie; Cutter, Asher D.; Weng, Zhiping; Claycomb, Julie M. (2015-01-01)
    As a champion of small RNA research for two decades, Caenorhabditis elegans has revealed the essential Argonaute CSR-1 to play key nuclear roles in modulating chromatin, chromosome segregation and germline gene expression via 22G-small RNAs. Despite CSR-1 being preserved among diverse nematodes, the conservation and divergence in function of the targets of small RNA pathways remains poorly resolved. Here we apply comparative functional genomic analysis between C. elegans and Caenorhabditis briggsae to characterize the CSR-1 pathway, its targets and their evolution. C. briggsae CSR-1-associated small RNAs that we identified by immunoprecipitation-small RNA sequencing overlap with 22G-RNAs depleted in cbr-csr-1 RNAi-treated worms. By comparing 22G-RNAs and target genes between species, we defined a set of CSR-1 target genes with conserved germline expression, enrichment in operons and more slowly evolving coding sequences than other genes, along with a small group of evolutionarily labile targets. We demonstrate that the association of CSR-1 with chromatin is preserved, and show that depletion of cbr-csr-1 leads to chromosome segregation defects and embryonic lethality. This first comparative characterization of a small RNA pathway in Caenorhabditis establishes a conserved nuclear role for CSR-1 and highlights its key role in germline gene regulation across multiple animal species.
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