Enemies join forces for gene insertion
[...]transposons themselves are more-efficient tools for gene addition5, because they encode a transposase enzyme that catalyses movement of transposon DNA to new genomic sites6. [...]TnsB might not be able to bind to natural target DNA in the absence of TnsC, which tethers it to DNA. [...]in the st...
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Published in | Nature (London) Vol. 613; no. 7945; pp. 1 - 2 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group
26.01.2023
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Subjects | |
Online Access | Get full text |
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Summary: | [...]transposons themselves are more-efficient tools for gene addition5, because they encode a transposase enzyme that catalyses movement of transposon DNA to new genomic sites6. [...]TnsB might not be able to bind to natural target DNA in the absence of TnsC, which tethers it to DNA. [...]in the structure reported by Park et al., the TnsC minifilament is positioned to contact target DNA on both sides of TnsB, perhaps to stabilize its bent form. [...]the authors observed that interactions between TnsB and TnsC caused a disordered segment of TnsB to fold and dock in a way that might help to stabilize bent target DNA. [...]the CAST system could potentially be used as a blueprint to establish programmable targeting of simpler transposons. |
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ISSN: | 0028-0836 1476-4687 |
DOI: | 10.1038/d41586-022-04584-6 |