Transactivation of miR-34a by p53 Broadly Influences Gene Expression and Promotes Apoptosis

Tsung Cheng Chang, Erik A. Wentzel, Oliver A. Kent, Kalyani Ramachandran, Michael Mullendore, Kwang Hyuck Lee, Georg Feldmann, Munekazu Yamakuchi, Marcella Ferlito, Charles J. Lowenstein, Dan E Arking, Michael A. Beer, Anirban Maitra, Joshua T. Mendell

Research output: Contribution to journalArticle

1464 Citations (Scopus)

Abstract

The p53 tumor suppressor protein is a critical regulator of the cellular response to cancer-initiating insults such as genotoxic stress. In this report, we demonstrate that microRNAs (miRNAs) are important components of the p53 transcriptional network. Global miRNA expression analyses identified a cohort of miRNAs that exhibit p53-dependent upregulation following DNA damage. One such miRNA, miR-34a, is commonly deleted in human cancers and, as shown here, frequently absent in pancreatic cancer cells. Characterization of the miR-34a primary transcript and promoter demonstrates that this miRNA is directly transactivated by p53. Expression of miR-34a causes dramatic reprogramming of gene expression and promotes apoptosis. Much like the known set of p53-regulated genes, miR-34a-responsive genes are highly enriched for those that regulate cell-cycle progression, apoptosis, DNA repair, and angiogenesis. Therefore, it is likely that an important function of miR-34a is the modulation and fine-tuning of the gene expression program initiated by p53.

Original languageEnglish (US)
Pages (from-to)745-752
Number of pages8
JournalMolecular Cell
Volume26
Issue number5
DOIs
StatePublished - Jun 8 2007

Fingerprint

p53 Genes
MicroRNAs
Transcriptional Activation
Gene Expression
DNA Damage
Apoptosis
Tumor Suppressor Protein p53
Gene Regulatory Networks
Pancreatic Neoplasms
DNA Repair
Neoplasms
Cell Cycle
Up-Regulation
Genes

Keywords

  • CELLCYCLE
  • RNA

ASJC Scopus subject areas

  • Molecular Biology

Cite this

Transactivation of miR-34a by p53 Broadly Influences Gene Expression and Promotes Apoptosis. / Chang, Tsung Cheng; Wentzel, Erik A.; Kent, Oliver A.; Ramachandran, Kalyani; Mullendore, Michael; Lee, Kwang Hyuck; Feldmann, Georg; Yamakuchi, Munekazu; Ferlito, Marcella; Lowenstein, Charles J.; Arking, Dan E; Beer, Michael A.; Maitra, Anirban; Mendell, Joshua T.

In: Molecular Cell, Vol. 26, No. 5, 08.06.2007, p. 745-752.

Research output: Contribution to journalArticle

Chang, TC, Wentzel, EA, Kent, OA, Ramachandran, K, Mullendore, M, Lee, KH, Feldmann, G, Yamakuchi, M, Ferlito, M, Lowenstein, CJ, Arking, DE, Beer, MA, Maitra, A & Mendell, JT 2007, 'Transactivation of miR-34a by p53 Broadly Influences Gene Expression and Promotes Apoptosis', Molecular Cell, vol. 26, no. 5, pp. 745-752. https://doi.org/10.1016/j.molcel.2007.05.010
Chang, Tsung Cheng ; Wentzel, Erik A. ; Kent, Oliver A. ; Ramachandran, Kalyani ; Mullendore, Michael ; Lee, Kwang Hyuck ; Feldmann, Georg ; Yamakuchi, Munekazu ; Ferlito, Marcella ; Lowenstein, Charles J. ; Arking, Dan E ; Beer, Michael A. ; Maitra, Anirban ; Mendell, Joshua T. / Transactivation of miR-34a by p53 Broadly Influences Gene Expression and Promotes Apoptosis. In: Molecular Cell. 2007 ; Vol. 26, No. 5. pp. 745-752.
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