The transcription factor atonal homolog 8 regulates Gata4 and friend of Gata-2 during vertebrate development

David R. Rawnsley, Jiping Xiao, John S. Lee, Xi Liu, Patricia Mericko-Ishizuka, Vinayak Kumar, Jie He, Arindam Basu, Min Min Lu, Francis C. Lynn, Michael Pack, Rosa Gasa, Mark L. Kahn

Research output: Contribution to journalArticle

16 Scopus citations

Abstract

Background: GATA and FOG proteins are critical transcriptional regulators of multiple organ systems in vertebrate development. Results: The transcription factor Atoh8 genetically interacts with Gata4 and Fog1 in zebrafish development and mouseATOH8 co-immunoprecipitates with FOG2. Conclusion: Atoh8 is a physical and genetic partner of Fog2 and GATA4. Significance: This study identifies Atoh8 as a transcriptional partner and regulator of the GATA-FOG transcriptional complex. GATA and Friend of GATA (FOG) form a transcriptional complex that plays a key role in cardiovascular development in both fish and mammals. In the present study we demonstrate that the basic helix-loop-helix transcription factor Atonal homolog 8 (Atoh8) is required for development of the heart in fish but not in mice. Genetic studies reveal that Atoh8 interacts specifically with Gata4 and Fog1 during development of the heart and swim bladder in the fish. Biochemical studies reveal that ATOH8, GATA4, and FOG2 associate in a single complex in vitro. In contrast to fish, ATOH8-deficient mice exhibit normal cardiac development and loss of ATOH8 does not alter cardiac development in Gata4+/- mice. This species difference in the role of ATOH8 is explained in part by LacZ and GFP reporter alleles that reveal restriction of Atoh8 expression to atrial but not ventricular myocardium in the mouse. Our findings identify ATOH8 as a novel regulator of GATA-FOG function that is required for cardiac development in the fish but not the mouse. Whether ATOH8 modulates GATA-FOG function at other sites or in more subtle ways in mammals is not yet known.

Original languageEnglish (US)
Pages (from-to)24429-24440
Number of pages12
JournalJournal of Biological Chemistry
Volume288
Issue number34
DOIs
StatePublished - Aug 23 2013

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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