Modeling cellular compartmentation in one-carbon metabolism

被引:40
|
作者
Scotti, Marco [1 ]
Stella, Lorenzo [1 ]
Shearer, Emily J. [2 ]
Stover, Patrick J. [2 ]
机构
[1] Microsoft Res Univ Trento, Ctr Computat & Syst Biol COSBI, Rovereto, Italy
[2] Cornell Univ, Div Nutr Sci, Ithaca, NY 14853 USA
关键词
CYSTATHIONINE BETA-SYNTHASE; METHIONINE ADENOSYLTRANSFERASE GENES; THYMIDYLATE BIOSYNTHESIS PATHWAY; S-ADENOSYLMETHIONINE SYNTHETASE; PYRIMIDINE NUCLEOTIDE CARRIER; GENOMIC DNA METHYLATION; ADENOSYL-L-METHIONINE; SERINE HYDROXYMETHYLTRANSFERASE; MATHEMATICAL-MODEL; METHYLENETETRAHYDROFOLATE REDUCTASE;
D O I
10.1002/wsbm.1209
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Folate-mediated one-carbon metabolism (FOCM) is associated with risk for numerous pathological states including birth defects, cancers, and chronic diseases. Although the enzymes that constitute the biological pathways have been well described and their interdependency through the shared use of folate cofactors appreciated, the biological mechanisms underlying disease etiologies remain elusive. The FOCM network is highly sensitive to nutritional status of several B-vitamins and numerous penetrant gene variants that alter network outputs, but current computational approaches do not fully capture the dynamics and stochastic noise of the system. Combining the stochastic approach with a rule-based representation will help model the intrinsic noise displayed by FOCM, address the limited flexibility of standard simulation methods for coarse-graining the FOCM-associated biochemical processes, and manage the combinatorial complexity emerging from reactions within FOCM that would otherwise be intractable. WIREs Syst Biol Med 2013, 5:343365. doi: 10.1002/wsbm.1209 For further resources related to this article, please visit the WIREs website.
引用
收藏
页码:343 / 365
页数:23
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