Poly(ADP-Ribosyl)ation of Chromosomal Proteins, Epigenetic Regulation and Human Genomic Integrity in Health and Disease

Author(s):  
Rafael Alvarez-Gonzalez
2010 ◽  
Vol 76 (6) ◽  
pp. 431-439 ◽  
Author(s):  
J. L. Fernández-Morera ◽  
V. Calvanese ◽  
S. Rodríguez-Rodero ◽  
E. Menéndez-Torre ◽  
M. F. Fraga

2018 ◽  
Vol 216 (2) ◽  
pp. 253-266 ◽  
Author(s):  
Yuxiang Zheng ◽  
Lewis C. Cantley

Folate metabolism is crucial for many biochemical processes, including purine and thymidine monophosphate (dTMP) biosynthesis, mitochondrial protein translation, and methionine regeneration. These biochemical processes in turn support critical cellular functions such as cell proliferation, mitochondrial respiration, and epigenetic regulation. Not surprisingly, abnormal folate metabolism has been causally linked with a myriad of diseases. In this review, we provide a historical perspective, delve into folate chemistry that is often overlooked, and point out various missing links and underdeveloped areas in folate metabolism for future exploration.


2016 ◽  
Vol 5 (3) ◽  
pp. 282-290 ◽  
Author(s):  
Marie-Claude Sincennes ◽  
Caroline E. Brun ◽  
Michael A. Rudnicki

Author(s):  
Maria Letizia Motti ◽  
Rosaria Meccariello

Epigenetics describes how both lifestyle and environment may affect human health through the modulation of genome functions and without any change to the DNA nucleotide sequence. The discovery of several epigenetic mechanisms and the possibility to deliver epigenetic marks in cells, gametes, and biological fluids has opened up new perspectives in the prevention, diagnosis, and treatment of human diseases. In this respect, the depth of knowledge of epigenetic mechanisms is fundamental to preserving health status and to developing targeted interventions. In this minireview, we summarize the epigenetic modulation of the KISS1 gene in order to provide an example of epigenetic regulation in health and disease.


Chromosoma ◽  
2012 ◽  
Vol 121 (2) ◽  
pp. 131-151 ◽  
Author(s):  
Angela K. Deem ◽  
Xuan Li ◽  
Jessica K. Tyler

2020 ◽  
Vol 13 (4) ◽  
pp. 289-310
Author(s):  
Hammad Ullah ◽  
Anna De Filippis ◽  
Cristina Santarcangelo ◽  
Maria Daglia

Diabetes mellitus (DM) is a chronic metabolic disorder and one of the most challenging health problems worldwide. Left untreated, it may progress causing serious complications. Genetics, epigenetics, and environmental factors are known to play an overlapping role in the pathogenesis of DM. Growing evidence suggests the hypothesis that the environment induces changes in the early phases of growth and development, influencing health and disease in the adulthood through the alteration in genetic expression of an individual, at least in part. DNA methylation, histone modifications and miRNAs are three mechanisms responsible for epigenetic alterations. The daily diet contains a number of secondary metabolites, with polyphenols being highest in abundance, which contribute to overall health and may prevent or delay the onset of many chronic diseases. Polyphenols have the ability to alter metabolic and signaling pathways at various levels, such as gene expression, epigenetic regulation, protein expression and enzyme activity. The potential efficacy of polyphenolic compounds on glucose homeostasis has been evidenced from in vitro, in vivo and clinical studies. The present review is designed to focus on epigenetic regulation exerted by polyphenolic compounds in DM and their complications, as well as to summarize clinical trials involving polyphenols in DM.


2019 ◽  
Vol 49 (11) ◽  
pp. 1371-1387 ◽  
Author(s):  
Guozhen Lu ◽  
Ming Zhang ◽  
Jian Wang ◽  
Kaixiang Zhang ◽  
Shengxi Wu ◽  
...  

2013 ◽  
Vol 41 (5) ◽  
pp. 2797-2806 ◽  
Author(s):  
S. Jorgensen ◽  
G. Schotta ◽  
C. S. Sorensen

Life ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1424
Author(s):  
Luisa Salvatori ◽  
Francesco Spallotta ◽  
Carlo Gaetano ◽  
Barbara Illi

Nitric oxide (NO) is a diffusible signaling molecule produced by three isoforms of nitric oxide synthase, which release NO during the metabolism of the amino acid arginine. NO participates in pathophysiological responses of many different tissues, inducing concentration-dependent effect. Indeed, while low NO levels generally have protective effects, higher NO concentrations induce cytotoxic/cytostatic actions. In recent years, evidences have been accumulated unveiling S-nitrosylation as a major NO-dependent post-translational mechanism ruling gene expression. S-nitrosylation is a reversible, highly regulated phenomenon in which NO reacts with one or few specific cysteine residues of target proteins generating S-nitrosothiols. By inducing this chemical modification, NO might exert epigenetic regulation through direct effects on both DNA and histones as well as through indirect actions affecting the functions of transcription factors and transcriptional co-regulators. In this light, S-nitrosylation may also impact on cancer cell gene expression programs. Indeed, it affects different cell pathways and functions ranging from the impairment of DNA damage repair to the modulation of the activity of signal transduction molecules, oncogenes, tumor suppressors, and chromatin remodelers. Nitrosylation is therefore a versatile tool by which NO might control gene expression programs in health and disease.


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