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    Date Issued2018 (1)2016 (1)Author
    Dokshin, Gregoriy A. (2)
    Mello, Craig C. (2)Bellott, Daniel W. (1)Carmell, Michelle A. (1)Enders, George C. (1)View MoreUMass Chan AffiliationRNA Therapeutics Institute (2)Graduate School of Biomedical Sciences (1)Document TypeJournal Article (2)KeywordCell Biology (1)CRISPR (1)Developmental Biology (1)developmental biology (1)Evolution (1)View MoreJournaleLife (1)Genetics (1)

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    Robust Genome Editing with Short Single-Stranded and Long, Partially Single-Stranded DNA Donors in Caenorhabditis elegans

    Dokshin, Gregoriy A.; Ghanta, Krishna S.; Piscopo, Katherine M.; Mello, Craig C. (2018-11-01)
    CRISPR-based genome editing using ribonucleoprotein complexes and synthetic single-stranded oligodeoxynucleotide (ssODN) donors can be highly effective. However, reproducibility can vary, and precise, targeted integration of longer constructs-such as green fluorescent protein tags remains challenging in many systems. Here, we describe a streamlined and optimized editing protocol for the nematode Caenorhabditis elegans We demonstrate its efficacy, flexibility, and cost-effectiveness by affinity-tagging 14 Argonaute proteins in C. elegans using ssODN donors. In addition, we describe a novel PCR-based, partially single-stranded, "hybrid" donor design that yields high efficiency editing with large (kilobase-scale) constructs. We use these hybrid donors to introduce fluorescent protein tags into multiple loci, achieving editing efficiencies that approach those previously obtained only with much shorter ssODN donors. The principals and strategies described here are likely to translate to other systems, and should allow researchers to reproducibly and efficiently obtain both long and short precision genome edits.
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    A widely employed germ cell marker is an ancient disordered protein with reproductive functions in diverse eukaryotes

    Carmell, Michelle A.; Dokshin, Gregoriy A.; Skaletsky, Helen; Hu, Yueh-Chiang; van Wolfswinkel, Josien C.; Igarashi, Kyomi J.; Bellott, Daniel W.; Nefedov, Michael; Reddien, Peter W.; Enders, George C.; et al. (2016-10-08)
    The advent of sexual reproduction and the evolution of a dedicated germline in multicellular organisms are critical landmarks in eukaryotic evolution. We report an ancient family of GCNA (germ cell nuclear antigen) proteins that arose in the earliest eukaryotes, and feature a rapidly evolving intrinsically disordered region (IDR). Phylogenetic analysis reveals that GCNA proteins emerged before the major eukaryotic lineages diverged; GCNA predates the origin of a dedicated germline by a billion years. Gcna gene expression is enriched in reproductive cells across eukarya - either just prior to or during meiosis in single-celled eukaryotes, and in stem cells and germ cells of diverse multicellular animals. Studies of Gcna-mutant C. elegans and mice indicate that GCNA has functioned in reproduction for at least 600 million years. Homology to IDR-containing proteins implicated in DNA damage repair suggests that GCNA proteins may protect the genomic integrity of cells carrying a heritable genome.
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