Chromatin as a key consumer in the metabolite economy

被引:60
作者
Diehl, Katharine L. [1 ,2 ]
Muir, Tom W. [1 ]
机构
[1] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
[2] Univ Utah, Dept Med Chem, Salt Lake City, UT 84112 USA
关键词
GLYCATION END-PRODUCTS; GENE-EXPRESSION; LYSINE; 2-HYDROXYISOBUTYRYLATION; HISTONE CROTONYLATION; ACETYLATION; COMPLEX; SUCCINYLATION; TRANSCRIPTION; PROPIONYLATION; BUTYRYLATION;
D O I
10.1038/s41589-020-0517-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This Perspective highlights emerging themes in the inter-regulation of the genome and metabolism via chromatin, including nonenzymatic histone modifications, cofactor-promiscuous chromatin-modifying enzymes, and subnucleocytoplasmic metabolite pools. In eukaryotes, chromatin remodeling and post-translational modifications (PTMs) shape the local chromatin landscape to establish permissive and repressive regions within the genome, orchestrating transcription, replication, and DNA repair in concert with other epigenetic mechanisms. Though cellular nutrient signaling encompasses a huge number of pathways, recent attention has turned to the hypothesis that the metabolic state of the cell is communicated to the genome through the type and concentration of metabolites in the nucleus that are cofactors for chromatin-modifying enzymes. Importantly, both epigenetic and metabolic dysregulation are hallmarks of a range of diseases, and this metabolism-chromatin axis may yield a well of new therapeutic targets. In this Perspective, we highlight emerging themes in the inter-regulation of the genome and metabolism via chromatin, including nonenzymatic histone modifications arising from chemically reactive metabolites, the expansion of PTM diversity from cofactor-promiscuous chromatin-modifying enzymes, and evidence for the existence and importance of subnucleocytoplasmic metabolite pools.
引用
收藏
页码:620 / 629
页数:10
相关论文
共 100 条
[1]   Advanced Glycation End Products: Association with the Pathogenesis of Diseases and the Current Therapeutic Advances [J].
Ajith, Thekkuttuparambil A. ;
Vinodkumar, Puzhikunathu .
CURRENT CLINICAL PHARMACOLOGY, 2016, 11 (02) :118-127
[2]   Methylglyoxal, the dark side of glycolysis [J].
Allaman, Igor ;
Belanger, Mireille ;
Magistretti, Pierre J. .
FRONTIERS IN NEUROSCIENCE, 2015, 9
[3]  
Allis C. D., 2015, EPIGENETICS
[4]  
[Anonymous], 2017, J PLANT BIOCH PHYSL
[5]   3-Deoxyglucosone: A Potential Glycating Agent Accountable for Structural Alteration in H3 Histone Protein through Generation of Different AGEs [J].
Ashraf, Jalaluddin M. ;
Ahmad, Saheem ;
Rabbani, Gulam ;
Hasan, Qambar ;
Jan, Arif Tasleem ;
Lee, Eun Ju ;
Khan, Rizwan Hasan ;
Alam, Khursheed ;
Choi, Inho .
PLOS ONE, 2015, 10 (02)
[6]   Physicochemical Analysis of Structural Alteration and Advanced Glycation End Products Generation During Glycation of H2A Histone by 3-Deoxyglucosone [J].
Ashraf, Jalaluddin M. ;
Ahmad, Saheem ;
Rabbani, Gulam ;
Jan, Arif Tasleem ;
Lee, Eun Ju ;
Khan, Rizwan Hasan ;
Choi, Inho .
IUBMB LIFE, 2014, 66 (10) :686-693
[7]   Site-Specific Reactivity of Nonenzymatic Lysine Acetylation [J].
Baeza, Josue ;
Smallegan, Michael J. ;
Denu, John M. .
ACS CHEMICAL BIOLOGY, 2015, 10 (01) :122-128
[8]   Glutarylation of Histone H4 Lysine 91 Regulates Chromatin Dynamics [J].
Bao, Xiucong ;
Liu, Zheng ;
Zhang, Wei ;
Gladysz, Kornelia ;
Fung, Yi Man Eva ;
Tian, Gaofei ;
Xiong, Ying ;
Wong, Jason Wing Hon ;
Yuen, Karen Wing Yee ;
Li, Xiang David .
MOLECULAR CELL, 2019, 76 (04) :660-+
[9]   Acetylation & Co: an expanding repertoire of histone acylations regulates chromatin and transcription [J].
Barnes, Claire E. ;
English, David M. ;
Cowley, Shaun M. .
DNA PACKAGING: NUCLEOSOME AND CHROMATIN, 2019, 63 (01) :97-107
[10]   An enquiry into metabolite domains [J].
Barros, L. Felipe ;
Martinez, Cristian .
BIOPHYSICAL JOURNAL, 2007, 92 (11) :3878-3884