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SRX1553600: GSM2051229: Control #3 Placenta; Bos indicus x Bos taurus; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2000) run: 47.1M spots, 4.7G bases, 2.4Gb downloads

Submitted by: NCBI (GEO)
Study: Global assessment of imprinted gene expression in the bovine conceptus by next generation sequencing
show Abstracthide Abstract
Genomic imprinting is an epigenetic mechanism that leads to parental-allele-specific gene expression. Approximately 150 imprinted genes have been identified in humans and mice but less than 30 genes have been described as imprinted in cattle. For the purpose of de novo identification of imprinted genes in bovine, we determined global monoallelic gene expression in brain, skeletal muscle, liver, kidney and placenta of day ~105 Bos taurus indicus X Bos taurus taurus F1 conceptuses using RNA sequencing. For this, we developed a bioinformatics pipeline to identify parental-specific SNPs after filtering A-to-I RNA editing sites. We identified 53 genes subject to monoallelic expression. A total of 23 are genes known to be imprinted in the cow and 7 are previously-characterized imprinted genes in human and/or mouse that have not be reported to be imprinted in cattle. Of the remaining 23 genes, we found that 10 are uncharacterized or unannotated transcripts located in known imprinting clusters, whereas the other 13 genes are distributed across the bovine genome and not close to any known imprinting clusters. To exclude potential cis-eQTL effects on allelic expression, we corroborated the parental specificity of monoallelic expression in day 86 Bos taurus taurus X Bos taurus taurus F1s and identified eight novel imprinted genes in bovine. Further, we identified 671 candidate A-to-I RNA editing sites and describe imprinted X inactivation in the bovine trophectoderm-derived CT1 cell line. Our results expand the imprinted gene list in bovine and demonstrate that monoallelic gene expression can be the result of cis-eQTL effect. Overall design: Identification of imprinted genes in brain, kidney, liver, skeletal muscle, and placenta of four day ~105 bovine conceptuses (The RNAseq data of brain, kidney, liver, and skeletal muscle have been deposited in GEO database under accession number: GSE63509)
Sample: Control #3 Placenta
SAMN04448268 • SRS1269507 • All experiments • All runs
Library:
Instrument: Illumina HiSeq 2000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Total RNA was isolated using Trizol Reagent (Invitrogen) according to the manufacturer's instructions. Semen DNA was isolated using phenol chloroform method. RNAseq libraries were prepared using Illumina TruSeq RNA sample preparation kit. Briefly, poly-A containing RNA was purified using magnetic beads with oligo-dT attached. The purified RNA was fragmented and used as a template for cDNA synthesis using random primers. In the following end-repair procedure, an "A" was added to the 3' end of the cDNA. The cDNA fragments with A-tailing were then ligated with T-tailing adaptors. PCR amplifications of cDNA fragments were followed to generate the final RNAseq library. Two DNaseq libraries (one with 350bp target insert size, the other with 550bp target insert size) were prepared using Illumina TruSeq DNA PCR-Free Sample Preparation Kit according to the manufacturer’s instructions (Illumina)
Experiment attributes:
GEO Accession: GSM2051229
Links:
Runs: 1 run, 47.1M spots, 4.7G bases, 2.4Gb
Run# of Spots# of BasesSizePublished
SRR313449647,081,6274.7G2.4Gb2016-08-17

ID:
2197754

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