Relationships among carbohydrate intermediate metabolites and DNA damage and repair in yeast from a systems biology perspective

被引:13
作者
Barea, Fernanda [1 ]
Bonatto, Diego [1 ]
机构
[1] UCS, Ctr Ciencias Biol & Saude, Inst Biotechnol, Lab Genet Toxicol, BR-95070560 Caxias Do Sul, Rio Grande Sul, Brazil
关键词
advanced glycation end products; DNA repair; literature data mining; protein-protein networks; reactive carbonyl species; systems biology;
D O I
10.1016/j.mrfmmm.2008.04.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Glucose and fructose are major dietary carbohydrates that are essential for general metabolism. The elevated consumption of these two monosaccharides by the human population is related to the development of pluri-metabolic syndromes (e.g., diabetes mellitus and obesity). Glucose and fructose are metabolized by specific biochemical pathways to generate energy and metabolites. Many of these metabolites are mono- and bi-phosphorylated compounds, which renders them likely to generate reactive carbonyl species (RCS). Under physiological conditions, RCS react non-enzymatically with macromolecules and small molecules by means of Maillard reactions, forming stable glycated/fructated compounds called advanced glycation end products (AGEs). DNA and dNTPs are prone to react with RCS, forming DNA- and dNTP-AGEs, and many of these compounds are genotoxic and/or mutagenic. Unfortunately, little is understood about the genotoxicity and/or mutagenicity of carbohydrate intermediate metabolites or their interactions with DNA repair and carbohydrate metabolic-associated proteins. To elucidate these associations between carbohydrate metabolic pathways, DNA repair mechanisms, and dNTP-/DNA-AGEs, a systems biology study was performed by employing algorithms to mine literature data and construct physical protein-protein interactions. The results obtained in this work allow us to construct a model suggesting that yeast carbohydrate metabolic-associated enzymes activate different mechanisms for DNA repair and dNTP synthesis and act during DNA replication to protect the genome against the effects of RCS. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:43 / 56
页数:14
相关论文
共 114 条
[1]   Consumption of sugars and the regulation of short-term satiety and food intake [J].
Anderson, GH ;
Woodend, D .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2003, 78 (04) :843S-849S
[2]   Correlation between acetaldehyde and ethanol resistance and expression of HSP genes in yeast strains isolated during the biological aging of sherry wines [J].
Aranda, A ;
Querol, A ;
del Olmo, ML .
ARCHIVES OF MICROBIOLOGY, 2002, 177 (04) :304-312
[3]  
ASP NG, 1994, AM J CLIN NUTR, V59, P679
[4]   Network biology:: Understanding the cell's functional organization [J].
Barabási, AL ;
Oltvai, ZN .
NATURE REVIEWS GENETICS, 2004, 5 (02) :101-U15
[5]   The role of AGEs in aging: causation or correlation [J].
Baynes, JW .
EXPERIMENTAL GERONTOLOGY, 2001, 36 (09) :1527-1537
[6]   From life to death - the struggle between chemistry and biology during aging: the Maillard reaction as an amplifier of genomic damage [J].
Baynes, JW .
BIOGERONTOLOGY, 2000, 1 (03) :235-246
[7]   PubMatrix: a tool for multiplex literature mining [J].
Becker, KG ;
Hosack, DA ;
Dennis, G ;
Lempicki, RA ;
Bright, TJ ;
Cheadle, C ;
Engel, J .
BMC BIOINFORMATICS, 2003, 4 (1)
[8]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[9]   Abasic sites in DNA:: repair and biological consequences in Saccharomyces cerevisiae [J].
Boiteux, S ;
Guillet, M .
DNA REPAIR, 2004, 3 (01) :1-12
[10]   A FAMILY OF HEXOSEPHOSPHATE MUTASES IN SACCHAROMYCES-CEREVISIAE [J].
BOLES, E ;
LIEBETRAU, W ;
HOFMANN, M ;
ZIMMERMANN, FK .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 220 (01) :83-96