The aim of this investigation is to understand molecular mechanisms of PUFA biosynthesis and regulation in order to enable the sustainable use of vegetable oils in aquafeeds as current sources of fish oils are unable to meet increasing demands for omega-3 PUFAs. By generating gene knockouts, we would like to study the genes that are crucial for multi-tissue synthesis of PUFA synthesis in vivo.
DOI: None
Zenodo URL: None
Created at: 20th Oct 2020 at 20:51
ELOVL2 Knockout
By generating CRISPR-mediated elovl2 knockout, we are planning to study the crucial role of elovl2 for multi-tissue synthesis of 22:6n-3 in vivo. Endogenously synthesized PUFAs are important for transcriptional regulation of lipogenic genes in Atlantic salmon. This study demonstrates key roles of elovl2 at two penultimate steps of PUFA synthesis in vivo and suggests Srebp-1 as a main regulator of endogenous PUFA synthesis in Atlantic salmon.
RNAseq
Stranded RNAseq libraries were prepared from 1µg total RNA from liver tissue using TruSeq Stranded mRNA library preparation kit (Illumina, San Diego, USA) using double unique indices (#20022371), according to the manufacturer's instruction (Part 15031057 Rev.E). Libraries were sequenced at the Norwegian Sequencing Centre (NSC). All libraries were pooled, and the same pool was sequenced on 4 flow cell lanes on a HiSeq 3000 machine (Illumina), generating 100bp single-end reads.
RNA sequencing files
...
Combined.counts
RNAseq data file, source: /mnt/users/fabig/DigiSal/crispr_RNAseq/samples_ELOVL2/final/2018-06-25_samples_ELOVL2/combined.counts
- combined.counts
Crispr_metadata
Meta data file,
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/meta/crispr_metadata.txt
- crispr_metadata.txt
Fatty Acid Analysis
Total lipids are extracted from tissues of white muscle, liver and whole brain from three fish per dietary treatment.
Initial FAD KO_Liver phospholipid fatty acid profile
Lipid data file
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/meta/Lipid_data
- Initial FAD KO_Liver phospholipid fatty acid profile.xlsx
Initial FAD KO_White muscle phospholipid fatty acid profile
Lipid data file
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/meta/Lipid_data
- Initial FAD KO_White muscle phospholipid fatty acid profile.xlsx
Sanger sequencing
The three different CRISPR target sites within the elovl2 gene (T1-3) were characterised by Sanger sequencing, sequencing on average 8 clones per individual.
FT1KO1.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- FT1KO1.fq
FT1KO2.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- FT1KO2.fq
FT1KO3.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- FT1KO3.fq
FT2KO1.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- FT2KO1.fq
FT2KO2.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- FT2KO2.fq
FT2KO5.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- FT2KO5.fq
FT3KO1.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- FT3KO1.fq
FT3KO2.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- FT3KO2.fq
FT3KO5.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- FT3KO5.fq
FT4KO1.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- FT4KO1.fq
FT4KO2.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- FT4KO2.fq
FT4KO3.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- FT4KO3.fq
T1KO2.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T1KO2.fq
T1KO3.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T1KO3.fq
T1KO4.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T1KO4.fq
T2KO1.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T2KO1.fq
T2KO2.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T2KO2.fq
T2KO4.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T2KO4.fq
T3KO1.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T3KO1.fq
T3KO2.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T3KO2.fq
T3KO3.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T3KO3.fq
T4KO1.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T4KO1.fq
T4KO2.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T4KO2.fq
T4KO3.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T4KO3.fq
T4KO4.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T4KO4.fq
T4KO5.fq
FASTQ file made from AB1 files.
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/sanger/data/fq
- T4KO5.fq
RNAseq-splicing
RNAseq is utilised to validate the SnpEff annotation predictions for aberrant splicing. For this purpose the percentage exon retention for exons 4, 6 and 7 are calculated using RNAseq data.
RNAseq data
RNAseq data file,
Source: /mnt/users/fabig/DigiSal/crispr_RNAseq/samples_ELOVL2/splicing/elovl2.splicing.txt
- elovl2.splicing.txt
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Created: 20th Oct 2020 at 20:51