2021
DOI: 10.1101/2021.02.12.430913
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KCTD19 associates with ZFP541 and HDAC1 and is required for meiotic exit in male mice

Abstract: Meiosis is a cell division process with complex chromosome events where various molecules must work in tandem. To find meiosis-related genes, we screened evolutionarily conserved and reproductive tract-enriched genes using the CRISPR/Cas9 system and identified potassium channel tetramerization domain containing 19 ( Kctd19 ) as an essential factor for meiosis. In prophase I, Kctd19 deficiency did not affect synapsis or the DNA damage response, and chiasma structures were also observed in metaphase I sperma… Show more

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Cited by 1 publication
(3 citation statements)
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References 48 publications
(64 reference statements)
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“…Our data, together with those from previous studies 5,11,23,30,45 , suggest a model for the evolutionarily conserved transcriptional architecture by which A-MYB and TCFL5 collaborate to reprogram gene expression at the onset of male meiosis I (Fig. 7).…”
Section: Discussionsupporting
confidence: 82%
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“…Our data, together with those from previous studies 5,11,23,30,45 , suggest a model for the evolutionarily conserved transcriptional architecture by which A-MYB and TCFL5 collaborate to reprogram gene expression at the onset of male meiosis I (Fig. 7).…”
Section: Discussionsupporting
confidence: 82%
“…Finally, the set of promoters bound by TCFL5 includes Kctd19 (Fig. 4e), a gene whose protein product is essential for meiotic exit 45 . The Kctd19 promoter is also bound by A-MYB.…”
Section: Mapping Tcfl5 Binding Across the Genomementioning
confidence: 99%
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