Total Nucleic Acid Extraction from Single Zebrafish Embryos for Genotyping and RNA-seq

被引:5
|
作者
Wali, Neha [1 ,3 ]
Merteroglu, Munise [2 ]
White, Richard J. [1 ,2 ]
Busch-Nentwich, Elisabeth M. [1 ,2 ]
机构
[1] Wellcome Sanger Inst, Cambridge, England
[2] Univ Cambridge, Cambridge Inst Therapeut Immunol & Infect Dis, Dept Med, Cambridge, England
[3] Wellcome Sanger Inst, Scientifc Operat, DNA Pipelines, Cambridge, England
来源
BIO-PROTOCOL | 2022年 / 12卷 / 01期
关键词
RNA-seq; Zebrafish; Transcriptomics; Genotyping;
D O I
10.21769/BioProtoc.4284
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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] .
引用
收藏
页数:10
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