RNA sequencing allows for the quantification of the transcriptome of embryos to investigate transcriptional responses to various perturbations (e.g., mutations, infections, drug treatments). Previous protocols either lack the option to genotype individual samples, or are laborious and therefore difficult to do at a large scale. We have developed a protocol to extract total nucleic acid from individual zebrafish embryos. Individual embryos are lysed in 96-well plates and nucleic acid is extracted using SPRI beads. The total nucleic acid can be genotyped and then DNase I treated to produce RNA samples for sequencing. This protocol allows for processing large numbers of individual samples, with the ability to genotype each sample, which makes it possible to undertake transcriptomic analysis on mutants at timepoints before the phenotype is visible. [GRAPHICS] .
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Univ British Columbia, Div Cardiol, 211-1033 Davie St, Vancouver, BC V6E 1M7, Canada
Univ British Columbia, Ctr Heart Lung Innovat, Vancouver, BC, Canada
Univ British Columbia, Ctr Cardiovasc Innovat, Vancouver, BC, CanadaUniv British Columbia, Div Cardiol, 211-1033 Davie St, Vancouver, BC V6E 1M7, Canada
Safabakhsh, Sina
Ma, Wei Feng
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Univ Virginia, Ctr Publ Hlth Genom, Dept Publ Hlth Sci, Charlottesville, VA USA
Univ Virginia, Med Scientist Training Program, Charlottesville, VA USAUniv British Columbia, Div Cardiol, 211-1033 Davie St, Vancouver, BC V6E 1M7, Canada
Ma, Wei Feng
Miller, Clint L. L.
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Univ Virginia, Ctr Publ Hlth Genom, Dept Publ Hlth Sci, Charlottesville, VA USAUniv British Columbia, Div Cardiol, 211-1033 Davie St, Vancouver, BC V6E 1M7, Canada
Miller, Clint L. L.
Laksman, Zachary
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Univ British Columbia, Div Cardiol, 211-1033 Davie St, Vancouver, BC V6E 1M7, Canada
Univ British Columbia, Ctr Heart Lung Innovat, Vancouver, BC, Canada
Univ British Columbia, Ctr Cardiovasc Innovat, Vancouver, BC, CanadaUniv British Columbia, Div Cardiol, 211-1033 Davie St, Vancouver, BC V6E 1M7, Canada