TY - JOUR
T1 - Functional and Pathological Roles of AHCY
AU - Vizán, Pedro
AU - Di Croce, Luciano
AU - Aranda, Sergi
N1 - Funding Information:
LD was supported by grants from the Spanish of Economy, Industry and Competitiveness (MEIC) (PID2019-108322GB-100), “Fundación Vencer El Cancer” (VEC), the European Regional Development Fund (FEDER), and from AGAUR. SA was funded by Ramón y Cajal Program MICIU-FSE (RYC2018-025002-I) and ISCIII-FEDER (PI19/01814). We acknowledge support of the Spanish Ministry of Science and Innovation to the EMBL partnership, the Centro de Excelencia Severo Ochoa and the CERCA Programme/Generalitat de Catalunya.
Publisher Copyright:
© Copyright © 2021 Vizán, Di Croce and Aranda.
PY - 2021/3/31
Y1 - 2021/3/31
N2 - Adenosylhomocysteinase (AHCY) is a unique enzyme and one of the most conserved proteins in living organisms. AHCY catalyzes the reversible break of S-adenosylhomocysteine (SAH), the by-product and a potent inhibitor of methyltransferases activity. In mammals, AHCY is the only enzyme capable of performing this reaction. Controlled subcellular localization of AHCY is believed to facilitate local transmethylation reactions, by removing excess of SAH. Accordingly, AHCY is recruited to chromatin during replication and active transcription, correlating with increasing demands for DNA, RNA, and histone methylation. AHCY deletion is embryonic lethal in many organisms (from plants to mammals). In humans, AHCY deficiency is associated with an incurable rare recessive disorder in methionine metabolism. In this review, we focus on the AHCY protein from an evolutionary, biochemical, and functional point of view, and we discuss the most recent, relevant, and controversial contributions to the study of this enzyme.
AB - Adenosylhomocysteinase (AHCY) is a unique enzyme and one of the most conserved proteins in living organisms. AHCY catalyzes the reversible break of S-adenosylhomocysteine (SAH), the by-product and a potent inhibitor of methyltransferases activity. In mammals, AHCY is the only enzyme capable of performing this reaction. Controlled subcellular localization of AHCY is believed to facilitate local transmethylation reactions, by removing excess of SAH. Accordingly, AHCY is recruited to chromatin during replication and active transcription, correlating with increasing demands for DNA, RNA, and histone methylation. AHCY deletion is embryonic lethal in many organisms (from plants to mammals). In humans, AHCY deficiency is associated with an incurable rare recessive disorder in methionine metabolism. In this review, we focus on the AHCY protein from an evolutionary, biochemical, and functional point of view, and we discuss the most recent, relevant, and controversial contributions to the study of this enzyme.
KW - S-adenosylhomocysteine hydrolase
KW - S-adenosylmethionine
KW - adenosylhomocysteinase
KW - chromatin
KW - embryo development
KW - epigenetics
KW - gene regulation
UR - http://www.scopus.com/inward/record.url?scp=85104201488&partnerID=8YFLogxK
U2 - 10.3389/fcell.2021.654344
DO - 10.3389/fcell.2021.654344
M3 - Review
AN - SCOPUS:85104201488
SN - 2296-634X
VL - 9
JO - Frontiers in Cell and Developmental Biology
JF - Frontiers in Cell and Developmental Biology
M1 - 654344
ER -