Abstract
A bold new effort to disrupt every gene in the mouse genome necessitates systematic, interdisciplinary approaches to analyzing patterning defects in the mouse embryo. We present a novel, rapid, and inexpensive method for obtaining high-resolution virtual histology for phenotypic assessment of mouse embryos. Using osmium tetroxide to differentially stain tissues followed by volumetric X-ray computed tomography to image whole embryos, isometric resolutions of 27 μm or 8 μm were achieved with scan times of 2 h or 12 h, respectively, using mid-gestation E9.5-E12.5 embryos. The datasets generated by this method are immediately amenable to state-of-the-art computational methods of organ patterning analysis. This technique to assess embryo anatomy represents a significant improvement in resolution, time, and expense for the quantitative, three-dimensional analysis of developmental patterning defects attributed to genetically engineered mutations and chemically induced embryotoxicity. © 2006 Johnson et al.
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CITATION STYLE
Johnson, J. T., Hansen, M. S., Wu, I., Healy, L. J., Johnson, C. R., Jones, G. M., … Keller, C. (2006). Virtual histology of transgenic mouse embryos for high-throughput phenotyping. PLoS Genetics, 2(4), 471–477. https://doi.org/10.1371/journal.pgen.0020061
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