» Articles » PMID: 28503659

Structure and Function of Histone Acetyltransferase MOF

Overview
Journal AIMS Biophys
Specialty Biophysics
Date 2017 May 16
PMID 28503659
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

MOF was first identified in as an important component of the dosage compensation complex. As a member of MYST family of histone acetyltransferase, MOF specifically deposits the acetyl groups to histone H4 lysine 16. Throughout evolution, MOF and its mammalian ortholog have retained highly conserved substrate specificity and similar enzymatic activities. MOF plays important roles in dosage compensation, ESC self-renewal, DNA damage and repair, cell survival, and gene expression regulation. Dysregulation of MOF has been implicated in tumor formation and progression of many types of human cancers. This review will discuss the structure and activity of mammalian hMOF as well as its function in H4K16 acetylation, DNA damage response, stem cell pluripotency, and carcinogenesis.

Citing Articles

Stabilization of MOF (KAT8) by USP10 promotes esophageal squamous cell carcinoma proliferation and metastasis through epigenetic activation of ANXA2/Wnt signaling.

Li P, Yang L, Park S, Liu F, Li A, Zhu Y Oncogene. 2024; 43(12):899-917.

PMID: 38317006 DOI: 10.1038/s41388-024-02955-z.


BAZ1B the Protean Protein.

Sharif S, Zamani N, Chadwick B Genes (Basel). 2021; 12(10).

PMID: 34680936 PMC: 8536118. DOI: 10.3390/genes12101541.


The Contribution of Histone Crotonylation to Tissue Health and Disease: Focus on Kidney Health.

Martinez-Moreno J, Fontecha-Barriuso M, Martin-Sanchez D, Sanchez-Nino M, Ruiz-Ortega M, Sanz A Front Pharmacol. 2020; 11:393.

PMID: 32308622 PMC: 7145939. DOI: 10.3389/fphar.2020.00393.


Molecular and epigenetic mechanisms of Cr(VI)-induced carcinogenesis.

Chen Q, Murphy A, Sun H, Costa M Toxicol Appl Pharmacol. 2019; 377:114636.

PMID: 31228494 PMC: 6658109. DOI: 10.1016/j.taap.2019.114636.


Corn dried distillers grains with solubles (cDDGS) in the diet of pigs change the expression of adipose genes that are potential therapeutic targets in metabolic and cardiovascular diseases.

Oczkowicz M, Szmatola T, Swiatkiewicz M, Pawlina-Tyszko K, Gurgul A, Zabek T BMC Genomics. 2018; 19(1):864.

PMID: 30509175 PMC: 6276254. DOI: 10.1186/s12864-018-5265-x.


References
1.
Rea S, Xouri G, Akhtar A . Males absent on the first (MOF): from flies to humans. Oncogene. 2007; 26(37):5385-94. DOI: 10.1038/sj.onc.1210607. View

2.
Sulli G, Di Micco R, dAdda di Fagagna F . Crosstalk between chromatin state and DNA damage response in cellular senescence and cancer. Nat Rev Cancer. 2012; 12(10):709-20. DOI: 10.1038/nrc3344. View

3.
Mizushima N, Levine B, Cuervo A, Klionsky D . Autophagy fights disease through cellular self-digestion. Nature. 2008; 451(7182):1069-75. PMC: 2670399. DOI: 10.1038/nature06639. View

4.
Brockdorff N, Turner B . Dosage compensation in mammals. Cold Spring Harb Perspect Biol. 2015; 7(3):a019406. PMC: 4355265. DOI: 10.1101/cshperspect.a019406. View

5.
Yuan H, Rossetto D, Mellert H, Dang W, Srinivasan M, Johnson J . MYST protein acetyltransferase activity requires active site lysine autoacetylation. EMBO J. 2011; 31(1):58-70. PMC: 3252582. DOI: 10.1038/emboj.2011.382. View