RNA Polymerase II transcription independent of TBP in murine embryonic stem cells

Author:

Kwan James ZJ1ORCID,Nguyen Thomas F1ORCID,Uzozie Anuli C23,Budzynski Marek A1,Cui Jieying1,Lee Joseph MC1,Van Petegem Filip1,Lange Philipp F23ORCID,Teves Sheila S1ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology, Life Sciences Institute, University of British Columbia

2. Department of Pathology and Laboratory Medicine, University of British Columbia

3. Michael Cuccione Childhood Cancer Research Program, BC Children’s Hospital Research Institute

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.

Funder

Canadian Institutes of Health Research

Natural Sciences and Engineering Research Council of Canada

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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