Identification of even a single gene that contributes to a complex trait provides insight into its molecular basis. However, multiple genes need to be identified if different genes affect a trait through different biological processes or pathways. In the context of pharmacological treatments, each gene is relevant to attaining effective therapy and avoiding adverse drug reactions. While both linkage mapping and association studies have proved to be effective tools for analysis of complex traits, they rarely identify more than one or a small number of genes per study and each gene requires considerable effort to fine-map. The goal of the proposed research is to use S. cerevisiae as a model system to understand the diversity of molecular mechanisms by which different genes affect colony color, a drug-dependent quantitative trait.
The first aim of the proposed research will determine whether multiple genes can be identified by a quantitative non-complementation screen using the yeast deletion collection. Reciprocal hemizygosity analysis will be used to estimate the rate of false positives due to haplo-insufficiency and second site mutations within the deletion collection.
The second aim of the proposed research will characterize the relationship between colony color alleles by identifying downstream changes in gene expression. A quantitative model of colony color will be generated based on changes in gene expression associated with colony color and the model's ability to predict the effects of genetic background will be tested using recombinant strains segregating both known and unknown colony color alleles. Together, these aims will provide insight into the diversity of molecular mechanisms by which different genes influence a trait and how their effects are modified by genetic background.

Public Health Relevance

Complex traits are the product of multiple genes, their interactions with each other, and their interactions with the environment. Although a number of methods are available to identify one or a few genes involved in a complex trait, it has been difficult to systematically identify every gene underlying a trait and the mechanisms by which they influence a trait. The proposed research will develop and evaluate a method of identifying multiple genes that contribute to complex traits and a model to predict their dependence on genetic background using gene expression data.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM086412-01A1
Application #
7736764
Study Section
Genetic Variation and Evolution Study Section (GVE)
Project Start
2009-09-29
Project End
2011-08-31
Budget Start
2009-09-29
Budget End
2010-08-31
Support Year
1
Fiscal Year
2009
Total Cost
$273,600
Indirect Cost
Name
Washington University
Department
Genetics
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Climer, Sharlee; Templeton, Alan R; Zhang, Weixiong (2015) Human gephyrin is encompassed within giant functional noncoding yin-yang sequences. Nat Commun 6:6534
Climer, Sharlee; Templeton, Alan R; Zhang, Weixiong (2014) Allele-specific network reveals combinatorial interaction that transcends small effects in psoriasis GWAS. PLoS Comput Biol 10:e1003766
Gan, Yanglan; Guan, Jihong; Zhou, Shuigeng et al. (2013) Identifying cis-Regulatory Elements and Modules using Conditional Random Fields. IEEE/ACM Trans Comput Biol Bioinform :
Kim, Hyun Seok; Huh, Juyoung; Riles, Linda et al. (2012) A noncomplementation screen for quantitative trait alleles in saccharomyces cerevisiae. G3 (Bethesda) 2:753-60
Zhang, Xiaoming; Xia, Jing; Lii, Yifan E et al. (2012) Genome-wide analysis of plant nat-siRNAs reveals insights into their distribution, biogenesis and function. Genome Biol 13:R20
Gan, Yanglan; Guan, Jihong; Zhou, Shuigeng et al. (2012) Structural features based genome-wide characterization and prediction of nucleosome organization. BMC Bioinformatics 13:49
Zhang, Weixiong; Zhou, Xuefeng; Xia, Jing et al. (2012) Identification of microRNAs and natural antisense transcript-originated endogenous siRNAs from small-RNA deep sequencing data. Methods Mol Biol 883:221-7
Zheng, Yun; Li, Yong-Fang; Sunkar, Ramanjulu et al. (2012) SeqTar: an effective method for identifying microRNA guided cleavage sites from degradome of polyadenylated transcripts in plants. Nucleic Acids Res 40:e28
Fay, Justin C (2011) Weighing the evidence for adaptation at the molecular level. Trends Genet 27:343-9
Ray, Monika; Zhang, Weixiong (2010) Analysis of Alzheimer's disease severity across brain regions by topological analysis of gene co-expression networks. BMC Syst Biol 4:136

Showing the most recent 10 out of 12 publications