Sex reversal following deletion of a single distal enhancer of Sox9

Cell fate decisions require appropriate regulation of key genes. , a direct target of SRY, is pivotal in mammalian sex determination. In vivo high-throughput chromatin accessibility techniques, transgenic assays, and genome editing revealed several novel gonadal regulatory elements in the 2-megabase...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 2018-06, Vol.360 (6396), p.1469-1473
Hauptverfasser: Gonen, Nitzan, Futtner, Chris R, Wood, Sophie, Garcia-Moreno, S Alexandra, Salamone, Isabella M, Samson, Shiela C, Sekido, Ryohei, Poulat, Francis, Maatouk, Danielle M, Lovell-Badge, Robin
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Sprache:eng
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Zusammenfassung:Cell fate decisions require appropriate regulation of key genes. , a direct target of SRY, is pivotal in mammalian sex determination. In vivo high-throughput chromatin accessibility techniques, transgenic assays, and genome editing revealed several novel gonadal regulatory elements in the 2-megabase gene desert upstream of Although others are redundant, enhancer 13 (Enh13), a 557-base pair element located 565 kilobases 5' from the transcriptional start site, is essential to initiate mouse testis development; its deletion results in XY females with transcript levels equivalent to those in XX gonads. Our data are consistent with the time-sensitive activity of SRY and indicate a strict order of enhancer usage. Enh13 is conserved and embedded within a 32.5-kilobase region whose deletion in humans is associated with XY sex reversal, suggesting that it is also critical in humans.
ISSN:0036-8075
1095-9203
DOI:10.1126/science.aas9408