Involvement of Human MOF in ATM Function

Abstract

We have determined that hMOF, the human ortholog of the Drosophila MOF gene (males absent on the first), encoding a protein with histone acetyltransferase activity, interacts with the ATM (ataxia-telangiectasia-mutated) protein. Cellular exposure to ionizing radiation (IR) enhances hMOF-dependent acetylation of its target substrate, lysine 16 (K16) of histone H4 independently of ATM function. Blocking the IR-induced increase in acetylation of histone H4 at K16, either by the expression of a dominant negative mutant ΔhMOF or by RNA interference-mediated hMOF knockdown, resulted in decreased ATM autophosphorylation, ATM kinase activity, and the phosphorylation of downstream effectors of ATM and DNA repair while increasing cell killing. In addition, decreased hMOF activity was associated with loss of the cell cycle checkpoint response to DNA double-strand breaks. The overexpression of wild-type hMOF yielded the opposite results, i.e., a modest increase in cell survival and enhanced DNA repair after IR exposure. These results suggest that hMOF influences the function of ATM.

ACKNOWLEDGMENTS

We thank K. D. Brown, M. B. Kastan, S. J. Elledge, B. D. Price, and J. Chen for providing us the constructs and antibodies. We thank S. J. Elledge, S. Elgin, Y. Shiloh, S. P. Jackson, C. Hunt, N. Horikoshi, S. N. Powell, and J. Eissenberg for their comments, suggestions, and helpful discussion.

This investigation was supported by NIH (NS34746, CA10445 [project 2]), the Department of Army, the A-T Children's Society, and funds from Radiation Oncology, Washington University School of Medicine, to T.K.P. and NCI grant PO1 CA97403 (project 5) to T.L.