Genetic correlates of gene expression in recombinant inbred strains - A relational model system to explore neurobehavioral phenotypes

被引:97
作者
Chesler, EJ [1 ]
Wang, JT
Lu, L
Qu, YH
Manly, KF
Williams, RW
机构
[1] Univ Tennessee, Ctr Hlth Sci, Dept Anat & Neurobiol, Ctr Genomics & Bioinformat, Memphis, TN 38163 USA
[2] Roswell Pk Canc Inst, Buffalo, NY 14263 USA
关键词
behavioral genetics; genetic correlation analysis; relational databases; QTL mapping; recombinant inbred mice; oligonucleotide microarray;
D O I
10.1385/NI:1:4:343
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
Full genome sequencing, high-density genotyping, expanding sets of microarray assays, and systematic phenotyping of neuroanatomical and behavioral traits are producing a wealth of data on the mouse central nervous system (CNS). These disparate resources are still poorly integrated. One solution is to acquire these data using a common reference population of isogenic lines of mice, providing a point of integration between the data types. Recombinant inbred (RI) mice, derived through inbreeding of progeny from an inbred cross, are a powerful tool for complex trait mapping and analysis of the challenging phenotypes of neuroscientific interest. These isogenic RI lines are a retrievable genetic resource that can be repeatedly studied using a wide variety of assays. Diverse data sets can be related through fixed and known genomes, using tools such as the interactive web-based system for complex trait analysis, www.WebQTL.org. In this report, we demonstrate the use of WebQTL to explore complex interactions among a wide variety of traits-from from mRNA transcripts to the impressive behavioral and pharmacological variation among RI strains. The relational approach exploiting a common set of strains facilitates study of multiple effects of single genes (pleiotropy) without a priori hypotheses required. Here we demonstrate the power of this technique through genetic correlation of gene expression with a database of neurobehavioral phenotypes collected in these strains of mice through more than 20 years of experimentation. By repeatedly studying the same panel, of mice, early data can be re-examined in light of technological advances unforeseen at the time of their initial collection.
引用
收藏
页码:343 / 357
页数:15
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