SIRT7 links H3K18 deacetylation to maintenance of oncogenic transformation

Matthew F. Barber, Eriko Michishita-Kioi, Yuanxin Xi, Luisa Tasselli, Mitomu Kioi, Zarmik Moqtaderi, Ruth I. Tennen, Silvana Paredes, Nicolas L. Young, Kaifu Chen, Kevin Struhl, Benjamin A. Garcia, Or Gozani, Wei Li () and Katrin F. Chua ()
Additional contact information
Matthew F. Barber: Stanford University, Stanford, California 94305, USA
Eriko Michishita-Kioi: Gerontology, and Metabolism, Stanford University, Stanford, California 94305, USA
Yuanxin Xi: Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA
Luisa Tasselli: Gerontology, and Metabolism, Stanford University, Stanford, California 94305, USA
Mitomu Kioi: Stanford University, Stanford, California 94305, USA
Zarmik Moqtaderi: Harvard Medical School, Boston, Massachusetts 02115, USA
Ruth I. Tennen: Gerontology, and Metabolism, Stanford University, Stanford, California 94305, USA
Silvana Paredes: Gerontology, and Metabolism, Stanford University, Stanford, California 94305, USA
Nicolas L. Young: Princeton University, Princeton, New Jersey 08544, USA
Kaifu Chen: Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA
Kevin Struhl: Harvard Medical School, Boston, Massachusetts 02115, USA
Benjamin A. Garcia: Princeton University, Princeton, New Jersey 08544, USA
Or Gozani: Stanford University, Stanford, California 94305, USA
Wei Li: Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, Texas 77030, USA
Katrin F. Chua: Gerontology, and Metabolism, Stanford University, Stanford, California 94305, USA

Nature, 2012, vol. 487, issue 7405, 114-118

Abstract: SIRT7 is an H3K18Ac-selective deacetylase that has a pivotal role in chromatin regulation, maintenance of cellular transformation programs and tumour formation in vivo.

Date: 2012
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DOI: 10.1038/nature11043

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