| Literature DB >> 35118175 |
Neha Wali1, Munise Merteroglu2, Richard J White1,2, Elisabeth M Busch-Nentwich1,2.
Abstract
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. Graphic abstract: Extraction of total nucleic acid from individual zebrafish embryos for genotyping and RNA-seq.Entities:
Keywords: Genotyping; RNA-seq; Transcriptomics; Zebrafish
Year: 2022 PMID: 35118175 PMCID: PMC8769753 DOI: 10.21769/BioProtoc.4284
Source DB: PubMed Journal: Bio Protoc ISSN: 2331-8325