Identification of QTLs controlling gene expression networks defined a priori

被引:89
作者
Kliebenstein, Daniel J.
West, Marilyn A. L.
van Leeuwen, Hans
Loudet, Olivier
Doerge, R. W.
St Clair, Dina A.
机构
[1] Univ Calif Davis, Dept Plant Sci, Davis, CA 95616 USA
[2] INRA, Stn Genet & Ameliorat Plantes, F-78026 Versailles, France
[3] Purdue Univ, Dept Stat, W Lafayette, IN 47907 USA
关键词
D O I
10.1186/1471-2105-7-308
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Gene expression microarrays allow the quantification of transcript accumulation for many or all genes in a genome. This technology has been utilized for a range of investigations, from assessments of gene regulation in response to genetic or environmental fluctuation to global expression QTL ( eQTL) analyses of natural variation. Current analysis techniques facilitate the statistical querying of individual genes to evaluate the significance of a change in response, also known as differential expression. Since genes are also known to respond as groups due to their membership in networks, effective approaches are needed to investigate transcriptome variation as related to gene network responses. Results: We describe a statistical approach that is capable of assessing higher-order a priori defined gene network response, as measured by microarrays. This analysis detected significant network variation between two Arabidopsis thaliana accessions, Bay-0 and Shahdara. By extending this approach, we were able to identify eQTLs controlling network responses for 18 out of 20 a priori-defined gene networks in a recombinant inbred line population derived from accessions Bay-0 and Shahdara. Conclusion: This approach has the potential to be expanded to facilitate direct tests of the relationship between phenotypic trait and transcript genetic architecture. The use of a priori definitions for network eQTL identification has enormous potential for providing direction toward future eQTL analyses.
引用
收藏
页数:17
相关论文
共 46 条
[1]   QTL analysis of lignification and cell wall digestibility in the Bay-0 x Shahdara RIL progeny of Arabidopsis thaliana as a model system for forage plant [J].
Barrière, Y ;
Laperche, A ;
Barrot, L ;
Aurel, G ;
Briand, M ;
Jouanin, L .
PLANT SCIENCE, 2005, 168 (05) :1235-1245
[2]  
Basten C.J., 1999, QTL Cartographer (Version 1.13)
[3]   Activation tagging identifies a conserved MYB regulator of phenylpropanoid biosynthesis [J].
Borevitz, JO ;
Xia, YJ ;
Blount, J ;
Dixon, RA ;
Lamb, C .
PLANT CELL, 2000, 12 (12) :2383-2393
[4]   Genetic dissection of transcriptional regulation in budding yeast [J].
Brem, RB ;
Yvert, G ;
Clinton, R ;
Kruglyak, L .
SCIENCE, 2002, 296 (5568) :752-755
[5]  
CHURCHILL GA, 1994, GENETICS, V138, P963
[6]   Gene expression data: The technology and statistical analysis [J].
Craig, BA ;
Black, MA ;
Doerge, RW .
JOURNAL OF AGRICULTURAL BIOLOGICAL AND ENVIRONMENTAL STATISTICS, 2003, 8 (01) :1-28
[7]   Proanthocyanidin-accumulating cells in Arabidopsis testa: Regulation of differentiation and role in seed development [J].
Debeaujon, I ;
Nesi, N ;
Perez, P ;
Devic, M ;
Grandjean, O ;
Caboche, M ;
Lepiniec, L .
PLANT CELL, 2003, 15 (11) :2514-2531
[8]   Identification of Botrytis cinerea susceptibility loci in Arabidopsis thaliana [J].
Denby, KJ ;
Kumar, P ;
Kliebenstein, DJ .
PLANT JOURNAL, 2004, 38 (03) :473-486
[9]   Leaf yellowing and anthocyanin accumulation are two genetically independent strategies in response to nitrogen limitation in Arabidopsis thaliana [J].
Diaz, U ;
Saliba-Colombani, V ;
Loudet, O ;
Belluomo, P ;
Moreau, L ;
Daniel-Vedele, F ;
Morot-Gaudry, JF ;
Maselaux-Daubresse, U .
PLANT AND CELL PHYSIOLOGY, 2006, 47 (01) :74-83
[10]  
Doerge RW, 1996, GENETICS, V142, P285