Allele-specific repression of Sox2 through the long non-coding RNA Sox2ot

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作者
Tobias C. Messemaker
Selina M. van Leeuwen
Patrick R. van den Berg
Anke E. J. ‘t Jong
Robert-Jan Palstra
Rob C. Hoeben
Stefan Semrau
Harald M. M. Mikkers
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[1] Leiden University Medical Center,Department of Molecular Cell Biology
[2] Leiden University Medical Center,Department of Rheumatology
[3] Leiden University,Leiden Institute of Physics
[4] Erasmus University Medical Center,Department of Biochemistry
[5] Ee634,undefined
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The transcription factor Sox2 controls the fate of pluripotent stem cells and neural stem cells. This gatekeeper function requires well-regulated Sox2 levels. We postulated that Sox2 regulation is partially controlled by the Sox2 overlapping long non-coding RNA (lncRNA) gene Sox2ot. Here we show that the RNA levels of Sox2ot and Sox2 are inversely correlated during neural differentiation of mouse embryonic stem cells (ESCs). Through allele-specific enhanced transcription of Sox2ot in mouse Sox2eGFP knockin ESCs we demonstrate that increased Sox2ot transcriptional activity reduces Sox2 RNA levels in an allele-specific manner. Enhanced Sox2ot transcription, yielding lower Sox2 RNA levels, correlates with a decreased chromatin interaction of the upstream regulatory sequence of Sox2 and the ESC-specific Sox2 super enhancer. Our study indicates that, in addition to previously reported in trans mechanisms, Sox2ot can regulate Sox2 by an allele-specific mechanism, in particular during development.
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