Abstract

BackgroundSelecting chromosome substitution strains (CSSs, also called consomic strains/lines) used in the search for quantitative trait loci (QTLs) consistently requires the identification of the respective phenotypic trait of interest and is simply based on a significant difference between a consomic and host strain. However, statistical significance as represented by P values does not necessarily predicate practical importance. We therefore propose a method that pays attention to both the statistical significance and the actual size of the observed effect. The present paper extends on this approach and describes in more detail the use of effect size measures (Cohen’s d, partial eta squared - ηp2) together with the P value as statistical selection parameters for the chromosomal assignment of QTLs influencing anxiety-related behavior and locomotion in laboratory mice.ResultsThe effect size measures were based on integrated behavioral z-scoring and were calculated in three experiments: (A) a complete consomic male mouse panel with A/J as the donor strain and C57BL/6J as the host strain. This panel, including host and donor strains, was analyzed in the modified Hole Board (mHB). The consomic line with chromosome 19 from A/J (CSS-19A) was selected since it showed increased anxiety-related behavior, but similar locomotion compared to its host. (B) Following experiment A, female CSS-19A mice were compared with their C57BL/6J counterparts; however no significant differences and effect sizes close to zero were found. (C) A different consomic mouse strain (CSS-19PWD), with chromosome 19 from PWD/PhJ transferred on the genetic background of C57BL/6J, was compared with its host strain. Here, in contrast with CSS-19A, there was a decreased overall anxiety in CSS-19PWD compared to C57BL/6J males, but not locomotion.ConclusionsThis new method shows an improved way to identify CSSs for QTL analysis for anxiety-related behavior using a combination of statistical significance testing and effect sizes. In addition, an intercross between CSS-19A and CSS-19PWD may be of interest for future studies on the genetic background of anxiety-related behavior.Electronic supplementary materialThe online version of this article (doi:10.1186/s12863-016-0411-4) contains supplementary material, which is available to authorized users.

Highlights

  • Selecting chromosome substitution strains (CSSs, called consomic strains/lines) used in the search for quantitative trait loci (QTLs) consistently requires the identification of the respective phenotypic trait of interest and is based on a significant difference between a consomic and host strain

  • The present paper extends on this approach and describes in more detail the use of effect size measurement (Cohen’s d and ηp2) in addition to significance testing as statistical selection parameters for the chromosomal assignment of quantitative trait locus (QTL) influencing modified Hole Board behavior in laboratory mice

  • In a previous article on the behavioral genetic analysis of a chromosome substitution strain panel we reduced the variety of modified Hole Board (mHB) measures to a small set of the summary scores using a principal component analysis (PCA) [8]

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Summary

Introduction

Selecting chromosome substitution strains (CSSs, called consomic strains/lines) used in the search for quantitative trait loci (QTLs) consistently requires the identification of the respective phenotypic trait of interest and is based on a significant difference between a consomic and host strain. Chromosome substitution strains (CSSs, referred to as consomic strains or lines) have been developed as a tool to identify chromosomes harboring quantitative trait loci (QTLs) for complex phenotypes, such as behavioral traits. The selection of chromosomes that contain at least one QTL is carried out through the relatively simple process of comparing the phenotypes of each consomic line with the host strain, i.e. identification of statistical significance for the phenotypic difference between the host and consomic strain. CSSs provide a tool for a more efficient genetic mapping by reducing the genetic complexity in a defined way [3, 4]

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