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Genes Dev. 2016 Jan 15;30(2):208-19. doi: 10.1101/gad.268714.115. Epub 2016 Jan 7.

MMP-9 facilitates selective proteolysis of the histone H3 tail at genes necessary for proficient osteoclastogenesis.

Author information

1
Department of Biochemistry and Molecular Biology, Norris Comprehensive Cancer Center, University of Southern California at Los Angeles, Los Angeles, California 90089, USA; Department of Biology, College of Natural Sciences, Chungbuk National University, Cheongju, Chungbuk 361-763, Republic of Korea;
2
Department of Medicine, Norris Comprehensive Cancer Center, University of Southern California at Los Angeles, Los Angeles, California 90089, USA;
3
Department of Biochemistry and Molecular Biology, Norris Comprehensive Cancer Center, University of Southern California at Los Angeles, Los Angeles, California 90089, USA;
4
Department of Biochemistry and Molecular Biology, Zilkha Neurogenetic Institute, University of Southern California at Los Angeles, Los Angeles, California 90089, USA;
5
Eli and Edythe Broad Center for Regenerative Medicine and Stem Cell Research, Department of Biochemistry and Molecular Biology, University of Southern California at Los Angeles, Los Angeles, California 90089, USA.

Abstract

Although limited proteolysis of the histone H3 N-terminal tail (H3NT) is frequently observed during mammalian differentiation, the specific genomic sites targeted for H3NT proteolysis and the functional significance of H3NT cleavage remain largely unknown. Here we report the first method to identify and examine H3NT-cleaved regions in mammals, called chromatin immunoprecipitation (ChIP) of acetylated chromatin (ChIPac). By applying ChIPac combined with deep sequencing (ChIPac-seq) to an established cell model of osteoclast differentiation, we discovered that H3NT proteolysis is selectively targeted near transcription start sites of a small group of genes and that most H3NT-cleaved genes displayed significant expression changes during osteoclastogenesis. We also discovered that the principal H3NT protease of osteoclastogenesis is matrix metalloproteinase 9 (MMP-9). In contrast to other known H3NT proteases, MMP-9 primarily cleaved H3K18-Q19 in vitro and in cells. Furthermore, our results support CBP/p300-mediated acetylation of H3K18 as a central regulator of MMP-9 H3NT protease activity both in vitro and at H3NT cleavage sites during osteoclastogenesis. Importantly, we found that abrogation of H3NT proteolysis impaired osteoclastogenic gene activation concomitant with defective osteoclast differentiation. Our collective results support the necessity of MMP-9-dependent H3NT proteolysis in regulating gene pathways required for proficient osteoclastogenesis.

KEYWORDS:

MMP-9; chromatin; epigenetic; histone; osteoclast; proteolysis

PMID:
26744418
PMCID:
PMC4719310
DOI:
10.1101/gad.268714.115
[Indexed for MEDLINE]
Free PMC Article

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