Journal article

The RING finger domain E3 ubiquitin ligases BRCA1 and the RNF20/RNF40 complex in global loss of the chromatin mark histone H2B monoubiquitination (H2Bub1) in cell line models and primary high-grade serous ovarian cancer

KA Dickson, AJ Cole, AJ Gill, A Clarkson, GB Gard, A Chou, CJ Kennedy, BR Henderson, S Fereday, N Traficante, K Alsop, DD Bowtell, A de Fazio, R Clifton-Bligh, DJ Marsh

Human Molecular Genetics | OXFORD UNIV PRESS | Published : 2016

Abstract

Enzymatic factors driving cancer-associated chromatin remodelling are of increasing interest as the role of the cancer epigenome in gene expression and DNA repair processes becomes elucidated. Monoubiquitination of histone H2B at lysine 120 (H2Bub1) is a central histone modification that functions in histone cross-talk, transcriptional elongation, DNA repair, maintaining centromeric chromatin and replication-dependent histone mRNA 3'-end processing, as well as being required for the differentiation of stem cells. The loss of global H2Bub1 is seen in a number of aggressive malignancies and has been linked to tumour progression and/or a poorer prognosis in some cancers. Here, we analyse a larg..

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Grants

Awarded by Medical Research and Materiel Command


Funding Acknowledgements

This work was supported by the Cancer Council NSW, Australia [RG13-10 to D.J.M., A.J.G. and G.B.G.]; Australian Research Council [FT100100489 to D.J.M]; National Health and Medical Research Council [APP1004799 to D.J.M], Australia Postgraduate Award and Sydney Medical School - Northern scholarship, Australia [to A.J.C.]. The Australian Ovarian Cancer Study was supported by the U.S. Army Medical Research and Materiel Command under DAMD17-01-1-0729, The Cancer Council Victoria, Queensland Cancer Fund, The Cancer Council New South Wales, The Cancer Council South Australia, The Cancer Foundation of Western Australia, The Cancer Council Tasmania and the National Health and Medical Research Council of Australia (NHMRC; ID400413, 10400281). The Gynecological Oncology Biobank at Westmead was funded by NHMRC Enabling Grants ID310670 & ID628903 and Cancer Institute NSW Grants 12/RIG/1-17 & 15/RIG/1-16. AdeF is funded by the University of Sydney Cancer Research Fund and the Cancer Institute NSW through the Sydney-West Translational Cancer Research Centre.