Yng1p Modulates the Activity of Sas3p as a Component of the Yeast NuA3 Histone Acetyltransferase Complex

Author:

Howe LeAnn1,Kusch Thomas1,Muster Nemone2,Chaterji Ranjana1,Yates John R.2,Workman Jerry L.1

Affiliation:

1. Howard Hughes Medical Institute, Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, Pennsylvania 16802-4500

2. Department of Cell Biology, The Scripps Research Institute, La Jolla, California 92037

Abstract

ABSTRACT The mammalian ING1 gene encodes a tumor suppressor required for the function of p53. In this study we report a novel function for YNG1 , a yeast homolog of ING1 . Yng1p is a stable component of the NuA3 histone acetyltransferase complex, which contains Sas3p, the yeast homolog of the mammalian MOZ proto-oncogene product, as its catalytic subunit. Yng1p is required for NuA3 function in vivo but surprisingly is not required for the integrity of the complex. Instead, we find that Yng1p mediates the interaction of Sas3p with nucleosomes and is thus required for the ability of NuA3 to modify histone tails. These data, and the observations that other ING1 homologs are found in additional yeast complexes that posttranslationally modify histones, suggest that members of the ING1 class of proteins may have broad roles in enhancing or modifying the activities of chromatin-modifying complexes, thereby regulating their activities in transcription control.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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