AI Article Synopsis

  • Transcription by RNA Polymerase II (Pol II) relies on the formation of a pre-initiation complex at the promoter, traditionally seen as dependent on the TATA-box binding protein (TBP).
  • Acute depletion of TBP in mouse embryonic stem cells does not significantly impact ongoing Pol II transcription, indicating a TBP-independent mechanism for transcriptional initiation.
  • While TBP affects RNA Polymerase III initiation, the TFIID complex remains functional with reduced factors, allowing Pol II transcription to continue efficiently without TBP.

Article Abstract

Transcription by RNA Polymerase II (Pol II) is initiated by the hierarchical assembly of the pre-initiation complex onto promoter DNA. Decades of research have shown that the TATA-box binding protein (TBP) is essential for Pol II loading and initiation. Here, we report instead that acute depletion of TBP in mouse embryonic stem cells has no global effect on ongoing Pol II transcription. In contrast, acute TBP depletion severely impairs RNA Polymerase III initiation. Furthermore, Pol II transcriptional induction occurs normally upon TBP depletion. This TBP-independent transcription mechanism is not due to a functional redundancy with the TBP paralog TRF2, though TRF2 also binds to promoters of transcribed genes. Rather, we show that the TFIID complex can form and, despite having reduced TAF4 and TFIIA binding when TBP is depleted, the Pol II machinery is sufficiently robust in sustaining TBP-independent transcription.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10174690PMC
http://dx.doi.org/10.7554/eLife.83810DOI Listing

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