FACT facilitates chromatin transcription by RNA polymerases I and III

Joanna L. Birch, Bertrand C-M Tan, Kostya I. Panov, Tatiana B. Panova, Jens S. Andersen, Tom A. Owen-Hughes, Jackie Russell, Sheng-Chung Lee, Joost C. B. M. Zomerdijk (Lead / Corresponding author)

    Research output: Contribution to journalArticlepeer-review

    76 Citations (Scopus)

    Abstract

    Efficient transcription elongation from a chromatin template requires RNA polymerases (Pols) to negotiate nucleosomes. Our biochemical analyses demonstrate that RNA Pol I can transcribe through nucleosome templates and that this requires structural rearrangement of the nucleosomal core particle. The subunits of the histone chaperone FACT (facilitates chromatin transcription), SSRP1 and Spt16, co-purify and co-immunoprecipitate with mammalian Pol I complexes. In cells, SSRP1 is detectable at the rRNA gene repeats. Crucially, siRNA-mediated repression of FACT subunit expression in cells results in a significant reduction in 47S pre-rRNA levels, whereas synthesis of the first 40nt of the rRNA is not affected, implying that FACT is important for Pol I transcription elongation through chromatin. FACT also associates with RNA Pol III complexes, is present at the chromatin of genes transcribed by Pol III and facilitates their transcription in cells. Our findings indicate that, beyond the established role in Pol II transcription, FACT has physiological functions in chromatin transcription by all three nuclear RNA Pols. Our data also imply that local chromatin dynamics influence transcription of the active rRNA genes by Pol I and of Pol III-transcribed genes.

    Original languageEnglish
    Pages (from-to)854-865
    Number of pages12
    JournalEMBO Journal
    Volume28
    Issue number7
    DOIs
    Publication statusPublished - 8 Apr 2009

    Keywords

    • rDNA chromatin
    • ribosomal RNA
    • transcription elongation
    • Spt16
    • SSRP1
    • RIBOSOMAL GENE-TRANSCRIPTION
    • UPSTREAM BINDING-FACTOR
    • REMODELING COMPLEX
    • SACCHAROMYCES-CEREVISIAE
    • HISTONE CHAPERONE
    • ACETYLTRANSFERASE ACTIVITY
    • NUCLEOLAR DOMINANCE
    • RDNA TRANSCRIPTION
    • HUMAN-CELLS
    • NUCLEOSOME

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