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SRX20094495: GSM7224990: immature oocytes 1A; Bos taurus; OTHER
1 ILLUMINA (Illumina NovaSeq 6000) run: 177.7M spots, 35.9G bases, 10.9Gb downloads

External Id: GSM7224990_r1
Submitted by: Sciences Animales, Université Laval
Study: Genome-wide methylation profile of mitochondrial DNA across bovine preimplantation development
show Abstracthide Abstract
This study characterized variations in the methylation profile of mitochondrial DNA (mtDNA) during initial bovine embryo development and correlated the presence of methylation with mtDNA transcription. Bovine oocytes were obtained from abattoir ovaries and submitted to in vitro culture procedures. Oocytes and embryos were collected at various stages (immature oocyte, IM; mature oocyte, MII; zygote, ZY; 4-cells, 4C; 16-cells, 16C and blastocysts, BL). Total DNA (including mtDNA) was used for Whole Genome Enzymatic Methyl Sequencing and for quantification of mtDNA copy number. Extracted RNA was used for quantification of mitochondrial transcripts (ND6, CYTB, tRNA-Phe and tRNA-Gln) using Droplet Digital PCR. The number of mtDNA copies per oocyte/embryo was found to be similar, while methylation levels in mtDNA varied among stages. Higher total methylation levels were found mainly at 4C and 16C. In specific gene regions, higher methylation levels were also observed at 4C and 16C (ND6, CYTB and tRNA-Phe), as well as an inverse correlation with the quantity of transcripts for these regions. This is a first description of epigenetic changes occurring in mtDNA during early embryonic development. Our results indicate that methylation might regulate the mtDNA transcription at a local level, particularly around the time of embryonic genome activation. Overall design: Bovine oocytes and embryos were collected at different developmental stages accross inital development (from immature oocyte to day 7 blastocyst)
Sample: immature oocytes 1A
SAMN34361187 • SRS17425995 • All experiments • All runs
Organism: Bos taurus
Library:
Name: GSM7224990
Instrument: Illumina NovaSeq 6000
Strategy: OTHER
Source: GENOMIC
Selection: other
Layout: PAIRED
Construction protocol: Bovine oocytes and embryos from all study groups were digested with proteinase K (50 mg/mL) in M-Digestion buffer 10X (Zymo Research) for 20 minutes at 50 oC to remove the zona pellucida. Then, they were submitted to total DNA extraction using QuickDNA Microprep Kit (Zymo Research; D3020) following the manufacturer protocol. Library construction was performed using the Enzymatic Methyl-Sequencing kit from New England Biolabs (E7120S), following the manufacturer protocol. Enzymatic Methyl-Sequencing
Runs: 1 run, 177.7M spots, 35.9G bases, 10.9Gb
Run# of Spots# of BasesSizePublished
SRR24299136177,682,58835.9G10.9Gb2024-04-24

ID:
27498144

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