Literature DB >> 26046647

OH, the Places You'll Go! Hydroxylation, Gene Expression, and Cancer.

Athanasios Ploumakis1, Mathew L Coleman2.   

Abstract

Hydroxylation is an emerging modification generally catalyzed by a family of ∼70 enzymes that are dependent on oxygen, Fe(II), ascorbate, and the Kreb's cycle intermediate 2-oxoglutarate (2OG). These "2OG oxygenases" sit at the intersection of nutrient availability and metabolism where they have the potential to regulate gene expression and growth in response to changes in co-factor abundance. Characterized 2OG oxygenases regulate fundamental cellular processes by catalyzing the hydroxylation or demethylation (via hydroxylation) of DNA, RNA, or protein. As such they have been implicated in various syndromes and diseases, but particularly cancer. In this review we discuss the emerging role of 2OG oxygenases in gene expression control, examine the regulation of these unique enzymes by nutrient availability and metabolic intermediates, and describe these properties in relation to the expanding role of these enzymes in cancer.
Copyright © 2015 Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 26046647     DOI: 10.1016/j.molcel.2015.05.026

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


  37 in total

1.  Tumors smother their epigenome.

Authors:  Bernard Thienpont; Laurien Van Dyck; Diether Lambrechts
Journal:  Mol Cell Oncol       Date:  2016-09-30

Review 2.  Amazing Diversity in Biochemical Roles of Fe(II)/2-Oxoglutarate Oxygenases.

Authors:  Caitlyn Q Herr; Robert P Hausinger
Journal:  Trends Biochem Sci       Date:  2018-04-27       Impact factor: 13.807

3.  Epigenetic modulation of β cells by interferon-α via PNPT1/mir-26a/TET2 triggers autoimmune diabetes.

Authors:  Mihaela Stefan-Lifshitz; Esra Karakose; Lingguang Cui; Abora Ettela; Zhengzi Yi; Weijia Zhang; Yaron Tomer
Journal:  JCI Insight       Date:  2019-03-07

Review 4.  New Insights into Protein Hydroxylation and Its Important Role in Human Diseases.

Authors:  Giada Zurlo; Jianping Guo; Mamoru Takada; Wenyi Wei; Qing Zhang
Journal:  Biochim Biophys Acta       Date:  2016-09-20

5.  Asparagine Hydroxylation is a Reversible Post-translational Modification.

Authors:  Javier Rodriguez; Cameron D Haydinger; Daniel J Peet; Lan K Nguyen; Alex von Kriegsheim
Journal:  Mol Cell Proteomics       Date:  2020-08-05       Impact factor: 5.911

6.  Bacillus anthracis Prolyl 4-Hydroxylase Modifies Collagen-like Substrates in Asymmetric Patterns.

Authors:  Nicholas J Schnicker; Mishtu Dey
Journal:  J Biol Chem       Date:  2016-04-21       Impact factor: 5.157

7.  RF-Hydroxysite: a random forest based predictor for hydroxylation sites.

Authors:  Hamid D Ismail; Robert H Newman; Dukka B Kc
Journal:  Mol Biosyst       Date:  2016-07-19

8.  Bacillus anthracis Prolyl 4-Hydroxylase Interacts with and Modifies Elongation Factor Tu.

Authors:  Nicholas J Schnicker; Mortezaali Razzaghi; Sanjukta Guha Thakurta; Srinivas Chakravarthy; Mishtu Dey
Journal:  Biochemistry       Date:  2017-10-19       Impact factor: 3.162

9.  Function and Regulation of Cph2 in Candida albicans.

Authors:  Shelley Lane; Pietro Di Lena; Kati Tormanen; Pierre Baldi; Haoping Liu
Journal:  Eukaryot Cell       Date:  2015-09-04

10.  Pathobiological Pseudohypoxia as a Putative Mechanism Underlying Myelodysplastic Syndromes.

Authors:  Yoshihiro Hayashi; Yue Zhang; Asumi Yokota; Xiaomei Yan; Jinqin Liu; Kwangmin Choi; Bing Li; Goro Sashida; Yanyan Peng; Zefeng Xu; Rui Huang; Lulu Zhang; George M Freudiger; Jingya Wang; Yunzhu Dong; Yile Zhou; Jieyu Wang; Lingyun Wu; Jiachen Bu; Aili Chen; Xinghui Zhao; Xiujuan Sun; Kashish Chetal; Andre Olsson; Miki Watanabe; Lindsey E Romick-Rosendale; Hironori Harada; Lee-Yung Shih; William Tse; James P Bridges; Michael A Caligiuri; Taosheng Huang; Yi Zheng; David P Witte; Qian-Fei Wang; Cheng-Kui Qu; Nathan Salomonis; H Leighton Grimes; Stephen D Nimer; Zhijian Xiao; Gang Huang
Journal:  Cancer Discov       Date:  2018-08-23       Impact factor: 39.397

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