Saccharomyces cerevisiae phenotypes can be predicted by using constraint-based analysis of a genome-scale reconstructed metabolic network

被引:252
作者
Famili, I
Forster, J
Nielson, J
Palsson, BO
机构
[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[2] Tech Univ Denmark, Bioctr, Ctr Proc Biotechnol, DK-2800 Lyngby, Denmark
关键词
D O I
10.1073/pnas.2235812100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Full genome sequences of prokaryotic organisms have led to reconstruction of genome-scale metabolic networks and in silico computation of their integrated functions. The first genome-scale metabolic reconstruction for a eukaryotic cell, Saccharomyces cerevisiae, consisting of 1,175 metabolic reactions and 733 metabolites, has appeared. A constraint-based in silico analysis procedure was used to compute properties of the S. cerevisiae metabolic network. The computed number of ATP molecules produced per pair of electrons donated to the electron transport system (ETS) and energy-maintenance requirements were quantitatively in agreement with experimental results. Computed whole-cell functions of growth and metabolic by-product secretion in aerobic and anaerobic Culture were consistent with experimental data, and thus mRNA expression profiles during metabolic shifts were computed. The computed consequences of gene knockouts on growth phenotypes were consistent with experimental observations. Thus, constraint-based analysis of a genome-scale metabolic network for the eukaryotic S. cerevisiae allows for computation of its integrated functions, producing in silico results that were consistent with observed phenotypic functions for approximate to70-80% of the conditions considered.
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页码:13134 / 13139
页数:6
相关论文
共 68 条
[1]   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
[2]   Identification and characterization of MAE1, the Saccharomyces cerevisiae structural gene encoding mitochondrial malic enzyme [J].
Boles, E ;
de Jong-Gubbels, P ;
Pronk, JT .
JOURNAL OF BACTERIOLOGY, 1998, 180 (11) :2875-2882
[3]  
BOLES E, 1997, YEAST SUGAR METABOLI, P81
[4]   Flux analysis of underdetermined metabolic networks: The quest for the missing constraints [J].
Bonarius, HPJ ;
Schmid, G ;
Tramper, J .
TRENDS IN BIOTECHNOLOGY, 1997, 15 (08) :308-314
[5]   Kinetic analysis of a molecular model of the budding yeast cell cycle [J].
Chen, KC ;
Csikasz-Nagy, A ;
Gyorffy, B ;
Val, J ;
Novak, B ;
Tyson, JJ .
MOLECULAR BIOLOGY OF THE CELL, 2000, 11 (01) :369-391
[6]   SGD:: Saccharomyces Genome Database [J].
Cherry, JM ;
Adler, C ;
Ball, C ;
Chervitz, SA ;
Dwight, SS ;
Hester, ET ;
Jia, YK ;
Juvik, G ;
Roe, T ;
Schroeder, M ;
Weng, SA ;
Botstein, D .
NUCLEIC ACIDS RESEARCH, 1998, 26 (01) :73-79
[7]   MUTANT STUDIES OF YEAST PHOSPHOFRUCTOKINASE [J].
CLIFTON, D ;
FRAENKEL, DG .
BIOCHEMISTRY, 1982, 21 (08) :1935-1942
[8]  
CLIFTON D, 1978, GENETICS, V88, P1
[9]   YPD™, PombePD™ and WormPD™:: model organism volumes of the BioKnowledge™ Library, an integrated resource for protein information [J].
Costanzo, MC ;
Crawford, ME ;
Hirschman, JE ;
Kranz, JE ;
Olsen, P ;
Robertson, LS ;
Skrzypek, MS ;
Braun, BR ;
Hopkins, KL ;
Kondu, P ;
Lengieza, C ;
Lew-Smith, JE ;
Tillberg, M ;
Garrels, JI .
NUCLEIC ACIDS RESEARCH, 2001, 29 (01) :75-79
[10]  
Covert MW, 2002, ASM NEWS, V68, P529