4.5 Article

Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory study

Journal

PHYSIOLOGICAL GENOMICS
Volume 34, Issue 3, Pages 243-255

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/physiolgenomics.90207.2008

Keywords

inbred mouse strains; test battery; open field; acoustic startle response; prepulse inhibition; rotarod; tail flick; SHIRPA; Y-maze; grip strength

Funding

  1. Medical Research Council [MC_UP_1502/1, MC_U142684172, MC_U142684173, MC_U142684175] Funding Source: Medline
  2. Medical Research Council [MC_U142684172, MC_U142684175, MC_UP_1502/1, MC_U142684173] Funding Source: researchfish
  3. MRC [MC_U142684173, MC_U142684175, MC_U142684172, MC_UP_1502/1] Funding Source: UKRI

Ask authors/readers for more resources

Mandillo S, Tucci V, Holter SM, Meziane H, Al Banchaabouchi M, Kallnik M, Lad HV, Nolan PM, Ouagazzal A-M, Coghill EL, Gale K, Golini E, Jacquot S, Krezel W, Parker A, Riet F, Schneider I, Marazziti D, Auwerx J, Brown SD, Chambon P, Rosenthal N, Tocchini-Valentini G, Wurst W. Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory study. Physiol Genomics 34: 243-255, 2008. First published May 27, 2008; doi:10.1152/physiolgenomics.90207.2008.-Establishing standard operating procedures (SOPs) as tools for the analysis of behavioral phenotypes is fundamental to mouse functional genomics. It is essential that the tests designed provide reliable measures of the process under investigation but most importantly that these are reproducible across both time and laboratories. For this reason, we devised and tested a set of SOPs to investigate mouse behavior. Five research centers were involved across France, Germany, Italy, and the UK in this study, as part of the EUMORPHIA program. All the procedures underwent a cross-validation experimental study to investigate the robustness of the designed protocols. Four inbred reference strains ( C57BL/6J, C3HeB/FeJ, BALB/cByJ, 129S2/SvPas), reflecting their use as common background strains in mutagenesis programs, were analyzed to validate these tests. We demonstrate that the operating procedures employed, which includes open field, SHIRPA, grip-strength, rotarod, Y-maze, prepulse inhibition of acoustic startle response, and tail flick tests, generated reproducible results between laboratories for a number of the test output parameters. However, we also identified several uncontrolled variables that constitute confounding factors in behavioral phenotyping. The EUMORPHIA SOPs described here are an important start-point for the ongoing development of increasingly robust phenotyping platforms and their application in large-scale, multicentre mouse phenotyping programs.

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