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            <name>Title</name>
            <description>A name given to the resource</description>
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                <text>Coronavirus</text>
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            <description>An account of the resource</description>
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                <text>Dominio científico: Coronavirus</text>
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      <name>Dublin Core</name>
      <description>The Dublin Core metadata element set is common to all Omeka records, including items, files, and collections. For more information see, http://dublincore.org/documents/dces/.</description>
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          <name>Title</name>
          <description>A name given to the resource</description>
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              <text>DNA interference by a mesophilic Argonaute protein, CbcAgo [version 2; peer review: 2 approved]</text>
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          <name>Creator</name>
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            <elementText elementTextId="11571">
              <text>Nieves García-Quintans, Laurie Bowden, José Berenguer, Mario Mencía</text>
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          <name>Description</name>
          <description>An account of the resource</description>
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              <text>Background: The search for putative enzymes that can facilitate gene editing has recently focused its attention on Argonaute proteins from prokaryotes (pAgos). Though they are structural homologues of human Argonaute protein, which uses RNA guides to interfere with RNA targets, pAgos use ssDNA guides to identify and, in many cases, cut a complementary DNA target. Thermophilic pAgos from Thermus thermophilus, Pyrococcus furiosus and Methanocaldococcus jasmanii have been identified and thoroughly studied, but their thermoactivity makes them of little use in mesophilic systems such as mammalian cells. Methods: Here we search for and identify CbcAgo, a prokaryotic Argonaute protein from a mesophilic bacterium, and characterize in vitro its DNA interference activity. Results: CbcAgo efficiently uses 5’P-ssDNA guides as small as 11-mers to cut ssDNA targets, requires divalent cations (preferentially, Mn2+) and has a maximum activity between 37 and 42 °C, remaining active up to 55 °C. Nicking activity on supercoiled dsDNA was shown. However, no efficient double-strand breaking activity could be demonstrated. Conclusions: CbcAgo can use gDNA guides as small as 11 nucleotides long to cut complementary ssDNA targets at 37ºC, making it a promising starting point for the development of new gene editing tools  for mammalian cells.</text>
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              <text>2020</text>
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          <name>Identifier</name>
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              <text>DOI: 10.12688/f1000research.18445.2</text>
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          <name>Source</name>
          <description>A related resource from which the described resource is derived</description>
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              <text>F1000Research</text>
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          <name>Publisher</name>
          <description>An entity responsible for making the resource available</description>
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              <text>F1000 Research Ltd</text>
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          <name>Coverage</name>
          <description>The spatial or temporal topic of the resource, the spatial applicability of the resource, or the jurisdiction under which the resource is relevant</description>
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              <text>Biology (General), Medicine</text>
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          <name>Language</name>
          <description>A language of the resource</description>
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            <elementText elementTextId="11578">
              <text>EN</text>
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