Identifying regulatory mechanisms using individual variation reveals key role for chromatin modification

被引:94
作者
Lee, Su-In
Pe'ert, Dana
Dudley, Aimee M.
Church, George M.
Koller, Daphne [1 ]
机构
[1] Stanford Univ, Dept Comp Sci, Stanford, CA 94305 USA
[2] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
关键词
expression phenotype; gene regulation; probabilistic model; regulatory network; association studies;
D O I
10.1073/pnas.0601852103
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
Sequence polymorphisms affect gene expression by perturbing the complex network of regulatory interactions. We propose a probabilistic method, called Geronemo, which directly aims to identify the mechanism by which genetic changes perturb the regulatory network. Geronemo automatically constructs a set of coregulated genes (modules), whose regulation can involve both sequence variations and expression of regulators. By exploiting the modularity of genetic regulatory systems, Geronemo reveals regulatory relationships that are indiscernible when genes are considered in isolation, allowing the recovery of intricate combinatorial regulation. By incorporating both expression and genotype of regulators, Geronemo captures cases where the effect of sequence variation on its targets is indirect. We applied Geronemo to a data set from the progeny generated by a cross between laboratory BY4716 (BY) and wild RM11-1a (RM) isolates of Saccharomyces cerevisiae. Geronemo produced previously undescribed hypotheses regarding genetic perturbations in the yeast regulatory network, including transcriptional regulation, signal transduction, and chromatin modification. In particular, we find a large number of modules that have both chromosomal characteristics and are regulated by chromatin modification proteins. Indeed, a large fraction of the variance in the expression can be explained by a small number of markers associated with chromatin modifiers. Additional analysis reveals positive selection for sequence evolution of elements in the Swi/Snf chromatin remodeling complex. Overall, our results suggest that a significant part of individual expression variation in yeast arises from evolution of a small number of chromatin structure modifiers.
引用
收藏
页码:14062 / 14067
页数:6
相关论文
共 29 条
[1]   A haplotype map of the human genome [J].
Altshuler, D ;
Brooks, LD ;
Chakravarti, A ;
Collins, FS ;
Daly, MJ ;
Donnelly, P ;
Gibbs, RA ;
Belmont, JW ;
Boudreau, A ;
Leal, SM ;
Hardenbol, P ;
Pasternak, S ;
Wheeler, DA ;
Willis, TD ;
Yu, FL ;
Yang, HM ;
Zeng, CQ ;
Gao, Y ;
Hu, HR ;
Hu, WT ;
Li, CH ;
Lin, W ;
Liu, SQ ;
Pan, H ;
Tang, XL ;
Wang, J ;
Wang, W ;
Yu, J ;
Zhang, B ;
Zhang, QR ;
Zhao, HB ;
Zhao, H ;
Zhou, J ;
Gabriel, SB ;
Barry, R ;
Blumenstiel, B ;
Camargo, A ;
Defelice, M ;
Faggart, M ;
Goyette, M ;
Gupta, S ;
Moore, J ;
Nguyen, H ;
Onofrio, RC ;
Parkin, M ;
Roy, J ;
Stahl, E ;
Winchester, E ;
Ziaugra, L ;
Shen, Y .
NATURE, 2005, 437 (7063) :1299-1320
[2]   Genomewide studies of histone deacetylase function in yeast [J].
Bernstein, BE ;
Tong, JK ;
Schreiber, SL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (25) :13708-13713
[3]   Genetic interactions between polymorphisms that affect gene expression in yeast [J].
Brem, RB ;
Storey, JD ;
Whittle, J ;
Kruglyak, L .
NATURE, 2005, 436 (7051) :701-703
[4]   The landscape of genetic complexity across 5,700 gene expression traits in yeast [J].
Brem, RB ;
Kruglyak, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (05) :1572-1577
[5]   Genetic dissection of transcriptional regulation in budding yeast [J].
Brem, RB ;
Yvert, G ;
Clinton, R ;
Kruglyak, L .
SCIENCE, 2002, 296 (5568) :752-755
[6]   Genetic and physical maps of Saccharomyces cerevisiae [J].
Cherry, JM ;
Ball, C ;
Weng, S ;
Juvik, G ;
Schmidt, R ;
Adler, C ;
Dunn, B ;
Dwight, S ;
Riles, L ;
Mortimer, RK ;
Botstein, D .
NATURE, 1997, 387 (6632) :67-73
[7]   Mapping determinants of human gene expression by regional and genome-wide association [J].
Cheung, VG ;
Spielman, RS ;
Ewens, KG ;
Weber, TM ;
Morley, M ;
Burdick, JT .
NATURE, 2005, 437 (7063) :1365-1369
[8]   Cis-acting expression quantitative trait loci in mice [J].
Doss, S ;
Schadt, EE ;
Drake, TA ;
Lusis, AJ .
GENOME RESEARCH, 2005, 15 (05) :681-691
[9]   Genome-wide identification of Isw2 chromatin-remodeling targets by localization of a catalytically inactive mutant [J].
Gelbart, ME ;
Bachman, N ;
Delrow, J ;
Boeke, JD ;
Tsukiyama, T .
GENES & DEVELOPMENT, 2005, 19 (08) :942-954
[10]   Transcriptional regulatory code of a eukaryotic genome [J].
Harbison, CT ;
Gordon, DB ;
Lee, TI ;
Rinaldi, NJ ;
Macisaac, KD ;
Danford, TW ;
Hannett, NM ;
Tagne, JB ;
Reynolds, DB ;
Yoo, J ;
Jennings, EG ;
Zeitlinger, J ;
Pokholok, DK ;
Kellis, M ;
Rolfe, PA ;
Takusagawa, KT ;
Lander, ES ;
Gifford, DK ;
Fraenkel, E ;
Young, RA .
NATURE, 2004, 431 (7004) :99-104