共 42 条
A Whole-Cell Computational Model Predicts Phenotype from Genotype
被引:856
作者:
Karr, Jonathan R.
[2
]
Sanghvi, Jayodita C.
[1
]
Macklin, Derek N.
[1
]
Gutschow, Miriam V.
[1
]
Jacobs, Jared M.
[1
]
Bolival, Benjamin
[1
]
Assad-Garcia, Nacyra, Jr.
[3
]
Glass, John I.
[3
]
Covert, Markus W.
[1
]
机构:
[1] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
[2] Stanford Univ, Grad Program Biophys, Stanford, CA 94305 USA
[3] J Craig Venter Inst, Rockville, MD 20850 USA
来源:
关键词:
GENOME-REDUCED BACTERIUM;
ESCHERICHIA-COLI;
RNA-POLYMERASE;
MINIMAL CELL;
MYCOPLASMA-GENITALIUM;
REPLICATION;
MOLECULE;
PROTEIN;
TIME;
DEHYDROGENASE;
D O I:
10.1016/j.cell.2012.05.044
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:
Understanding how complex phenotypes arise from individual molecules and their interactions is a primary challenge in biology that computational approaches are poised to tackle. We report a whole-cell computational model of the life cycle of the human pathogen Mycoplasma genitalium that includes all of its molecular components and their interactions. An integrative approach to modeling that combines diverse mathematics enabled the simultaneous inclusion of fundamentally different cellular processes and experimental measurements. Our whole-cell model accounts for all annotated gene functions and was validated against a broad range of data. The model provides insights into many previously unobserved cellular behaviors, including in vivo rates of protein-DNA association and an inverse relationship between the durations of DNA replication initiation and replication. In addition, experimental analysis directed by model predictions identified previously undetected kinetic parameters and biological functions. We conclude that comprehensive whole-cell models can be used to facilitate biological discovery.
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页码:389 / 401
页数:13
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