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Histone demethylase KDM2A: Biological functions and clinical values (Review).
Liu, Lisheng; Liu, Jiangnan; Lin, Qinghai.
Affiliation
  • Liu L; Key Laboratory of Animal Resistance Research, College of Life Science, Shandong Normal University, Jinan, Shandong 250014, P.R. China.
  • Liu J; Department of Clinical Laboratory, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong 250117, P.R. China.
  • Lin Q; Department of Cell and Molecular Biology, Karolinska Institutet, Stockholm, SE-171 77, Sweden.
Exp Ther Med ; 22(1): 723, 2021 Jul.
Article de En | MEDLINE | ID: mdl-34007332
ABSTRACT
Histone lysine demethylation modification is a critical epigenetic modification. Lysine demethylase 2A (KDM2A), a Jumonji C domain-containing demethylase, demethylates the dimethylated H3 lysine 36 (H3K36) residue and exerts little or no activity on monomethylated and trimethylated H3K36 residues. KDM2A expression is regulated by several factors, such as microRNAs, and the phosphorylation of KDM2A also plays a vital role in its function. KDM2A mainly recognizes the unmethylated region of CpG islands and subsequently demethylates histone H3K36 residues. In addition, KDM2A recognizes and binds to phosphorylated proteins, and promotes their ubiquitination and degradation. KDM2A plays an important role in chromosome remodeling and gene transcription, and is involved in cell proliferation and differentiation, cell metabolism, heterochromosomal homeostasis and gene stability. Notably, KDM2A is crucial for tumorigenesis and progression. In the present review, the documented biological functions of KDM2A in physiological and pathological processes are comprehensively summarized.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Exp Ther Med Année: 2021 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Exp Ther Med Année: 2021 Type de document: Article