Abstract
Differences in the number of functionally and/or phenotypically defined bone marrow cells in inbred mouse strains have been exploited to map quantitative trait loci (QTL) that determine the variation in cell frequency. To extend this approach to the differences in the stem/progenitor cell compartment in CBA/H and C57BL/6 mice, we have exploited the resolution of flow cytometry and the power of QTL analyses in 124 F2 mice to analyze lineage-negative (Lin−) bone marrow cells according to the intensity of labeling with Sca-1 and c-Kit. In the Lin− Sca-1+ c-Kit+ enriched population, six QTL were identified: one significant and five suggestive. Whereas previous in vitro clonogenic, LTC-IC, day 35 CAFC, and flow cytometry each identified different QTL, our approach identified the same or very similar QTL at all three loci (chromosomes 1, 17, and 18) as well as QTL on chromosomes 6 and 10. In silico analyses implicate hematopoietic stem cell homing involving Cxcr4 and Cxcl12 as being the determining pathway. The mapping of the same or very similar QTL in independent studies using different assay(s) suggests a common genetic determinant, and thus reinforces the biological and genetic significance of the QTL. These data also suggest that mouse bone marrow cell subpopulations can be functionally, phenotypically, and genetically defined.
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Acknowledgments
This work was supported by the Leukaemia Research Fund. CC was funded by an MRC Research Studentship, and GG was supported by the HOPE Foundation for Cancer Research. The authors dedicate this article to Mark Plumb, who was the principal investigator on this project and died in May 2007.
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Jawad, M., Cole, C., Zanker, A. et al. QTL analyses of lineage-negative mouse bone marrow cells labeled with Sca-1 and c-Kit. Mamm Genome 19, 190–198 (2008). https://doi.org/10.1007/s00335-008-9097-x
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DOI: https://doi.org/10.1007/s00335-008-9097-x