High-Confidence Discovery of Genetic Network Regulators in Expression Quantitative Trait Loci Data

被引:8
|
作者
Duarte, Christine W. [1 ]
Zeng, Zhao-Bang [2 ,3 ,4 ]
机构
[1] Univ Alabama, Dept Biostat, Sect Stat Genet, Birmingham, AL 35294 USA
[2] N Carolina State Univ, Bioinformat Res Ctr, Raleigh, NC 27695 USA
[3] N Carolina State Univ, Dept Stat, Raleigh, NC 27695 USA
[4] N Carolina State Univ, Dept Genet, Raleigh, NC 27695 USA
基金
美国国家科学基金会;
关键词
INTEGRATIVE GENOMICS APPROACH; SEGREGATING POPULATIONS; TRANSCRIPTION FACTORS; INFERENCE; YEAST;
D O I
10.1534/genetics.110.124685
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Expression QTL (eQTL) studies involve the collection of microarray gene expression data and genetic marker data from segregating individuals in a population to search for genetic determinants of differential gene expression. Previous studies have found large numbers of trans-regulated genes (regulated by unlinked genetic loci) that link to a single locus or eQTL "hotspot,'' and it would be desirable to find the mechanism of coregulation for these gene groups. However, many difficulties exist with current network reconstruction algorithms such as low power and high computational cost. A common observation for biological networks is that they have a scale-free or power-law architecture. In such an architecture, highly influential nodes exist that have many connections to other nodes. If we assume that this type of architecture applies to genetic networks, then we can simplify the problem of genetic network reconstruction by focusing on discovery of the key regulatory genes at the top of the network. We introduce the concept of "shielding'' in which a specific gene expression variable (the shielder) renders a set of other gene expression variables (the shielded genes) independent of the eQTL. We iteratively build networks from the eQTL to the shielder down using tests of conditional independence. We have proposed a novel test for controlling the shielder false-positive rate at a predetermined level by requiring a threshold number of shielded genes per shielder. Using simulation, we have demonstrated that we can control the shielder false-positive rate as well as obtain high shielder and edge specificity. In addition, we have shown our method to be robust to violation of the latent variable assumption, an important feature in the practical application of our method. We have applied our method to a yeast expression QTL data set in which microarray and marker data were collected from the progeny of a backcross of two species of Saccharomyces cerevisiae (Brem et al. 2002). Seven genetic networks have been discovered, and bioinformatic analysis of the discovered regulators and corresponding regulated genes has generated plausible hypotheses for mechanisms of regulation that can be tested in future experiments.
引用
收藏
页码:955 / 964
页数:10
相关论文
共 50 条
  • [31] Improved confidence intervals in quantitative trait loci mapping by permutation bootstrapping
    Bennewitz, J
    Reinsch, N
    Kahn, E
    GENETICS, 2002, 160 (04) : 1673 - 1686
  • [32] Quantitative trait loci analysis using the false discovery rate
    Benjamini, Y
    Yekutieli, D
    GENETICS, 2005, 171 (02) : 783 - 789
  • [33] Discovery of Quantitative Trait Loci for Plant Architecture in Diploid Rosa
    Young, Ellen L.
    Wu, Xuan
    Liang, Shuyin
    Yan, Muqing
    van de Weg, Eric
    Klein, Patricia
    Byrne, David
    HORTSCIENCE, 2018, 53 (09) : S338 - S338
  • [34] Promoter-interacting expression quantitative trait loci are enriched for functional genetic variants
    Chandra, Vivek
    Bhattacharyya, Sourya
    Schmiedel, Benjamin J.
    Madrigal, Ariel
    Gonzalez-Colin, Cristian
    Fotsing, Stephanie
    Crinklaw, Austin
    Seumois, Gregory
    Mohammadi, Pejman
    Kronenberg, Mitchell
    Peters, Bjoern
    Ay, Ferhat
    Vijayanand, Pandurangan
    NATURE GENETICS, 2021, 53 (01) : 110 - 119
  • [35] Promoter-interacting expression quantitative trait loci are enriched for functional genetic variants
    Vivek Chandra
    Sourya Bhattacharyya
    Benjamin J. Schmiedel
    Ariel Madrigal
    Cristian Gonzalez-Colin
    Stephanie Fotsing
    Austin Crinklaw
    Gregory Seumois
    Pejman Mohammadi
    Mitchell Kronenberg
    Bjoern Peters
    Ferhat Ay
    Pandurangan Vijayanand
    Nature Genetics, 2021, 53 : 110 - 119
  • [36] Modeling tenderness for genetic and quantitative trait loci analyses
    Chang, L. Y.
    Pitchford, W. S.
    Bottema, C. D. K.
    JOURNAL OF ANIMAL SCIENCE, 2014, 92 (01) : 39 - 47
  • [38] Rapid identification of high-confidence taxonomic assignments for metagenomic data
    MacDonald, Norman J.
    Parks, Donovan H.
    Beiko, Robert G.
    NUCLEIC ACIDS RESEARCH, 2012, 40 (14)
  • [39] Discovery and analysis of methylation quantitative trait loci (mQTLs) mapping to novel osteoarthritis genetic risk signals
    Rice, S. J.
    Cheung, K.
    Reynard, L. N.
    Loughlin, J.
    OSTEOARTHRITIS AND CARTILAGE, 2019, 27 (10) : 1545 - 1556
  • [40] High-Confidence Data Programming for Evaluating Suppression of Physiological Alarms
    Pugh, Sydney
    Ruchkin, Ivan
    Bonafide, Christopher P.
    DeMauro, Sara B.
    Sokolsky, Oleg
    Lee, Insup
    Weimer, James
    2021 IEEE/ACM CONFERENCE ON CONNECTED HEALTH: APPLICATIONS, SYSTEMS AND ENGINEERING TECHNOLOGIES (CHASE 2021), 2021, : 70 - 81