ERK-dependent phosphorylation of the transcription initiation factor TIF-IA is required for RNA polymerase I transcription and cell growth.
Research output: Contribution to journal › Journal article › Research › peer-review
Phosphorylation of transcription factors by mitogen-activated protein kinase (MAPK) cascades links cell signaling with the control of gene expression. Here we show that growth factors induce rRNA synthesis by activating MAPK-dependent signaling cascades that target the RNA polymerase I-specific transcription initiation factor TIF-IA. Activation of TIF-IA and ribosomal gene transcription is sensitive to PD98059, indicating that TIF-IA is targeted by MAPK in vivo. Phosphopeptide mapping and mutational analysis reveals two serine residues (S633 and S649) that are phosphorylated by ERK and RSK kinases. Replacement of S649 by alanine inactivates TIF-IA, inhibits pre-rRNA synthesis, and retards cell growth. The results provide a link between growth factor signaling, ribosome production, and cell growth, and may have a major impact on the mechanism of cell transformation.
Original language | English |
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Journal | Molecular Cell |
Volume | 11 |
Issue number | 2 |
Pages (from-to) | 405-13 |
Number of pages | 8 |
ISSN | 1097-2765 |
Publication status | Published - 2003 |
Bibliographical note
Keywords: 3T3 Cells; Amino Acid Sequence; Animals; Cell Division; Cell Line; Humans; MAP Kinase Signaling System; Mice; Mitogen-Activated Protein Kinases; Mitogens; Molecular Sequence Data; Phosphorylation; Protein Kinases; RNA Polymerase I; RNA, Ribosomal; Recombinant Proteins; Ribosomal Protein S6 Kinases; Transcription Factors; Transcription, Genetic
ID: 5015173