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SRX17606338: GSM6588592: Control_#4 Muscle; Bos indicus x Bos taurus; RNA-Seq
2 ILLUMINA (Illumina HiSeq 4000) runs: 42.4M spots, 12.7G bases, 5.1Gb downloads

External Id: GSM6588592_r1
Submitted by: Division of Animal Sciences, University of Missouri, Columbia
Study: Differentially expressed tRNA-derived fragments in bovine fetuses with assisted reproduction induced congenital overgrowth syndrome
show Abstracthide Abstract
Background: As couples struggle with infertility and livestock producers wish to rapidly improve genetic merit in their herd, assisted reproductive technologies (ART) have become increasingly popular in human medicine as well as the livestock industry. Utilizing ART can cause an increased risk of congenital overgrowth syndromes, such as Large Offspring Syndrome (LOS) in ruminants. A dysregulation of transcripts has been observed in bovine fetuses with LOS, which is suggested to be a cause of the phenotype. Our recent study identified variations in tRNA expression in LOS individuals, leading us to hypothesize that variations in tRNA expression can influence the availability of their processed regulatory products, tRNA-derived fragments (tRFs). Due to their resemblance in size to microRNAs, studies suggest that tRFs target mRNA transcripts and regulate gene expression. Thus, we have sequenced small RNA isolated from skeletal muscle and liver of day 105 bovine fetuses to elucidate the mechanisms contributing to LOS. Moreover, we have utilized our previously generated tRNA sequencing data to analyze the contribution of tRNA availability to tRF abundance. Results: 22,289 and 7,737 unique tRFs were predicted in the liver and muscle tissue respectively. The greatest number of reads originated from 5' tRFs in muscle and 5' halves in liver. In addition, mitochondrial (MT) and nuclear derived tRF expression was tissue-specific with most MT-tRFs and nuclear tRFs derived from LysUUU and iMetCAU in muscle, and AsnGUU and GlyGCC in liver. Despite variation in tRF abundance within treatment groups, we identified differentially expressed (DE) tRFs across Control-AI, ART-Normal, and ART-LOS groups with the most DE tRFs between ART-Normal and ART-LOS groups. Many DE tRFs target transcripts enriched in pathways related to growth and development in the muscle and tumor development in the liver. Finally, we found positive correlation coefficients between tRNA availability and tRF expression in muscle (R = 0.47) and liver (0.6). Conclusion: Our results highlight the dysregulation of tRF expression and its regulatory roles in LOS. These tRFs were found to target both imprinted and non-imprinted genes in muscle as well as genes linked to tumor development in the liver. Furthermore, we found that tRNA transcription is a highly modulated event that plays a part in the biogenesis of tRFs. This study is the first to investigate the relationship between tRNA and tRF expression in combination with ART-induced LOS. Overall design: RNA sequencing for kidney, liver, and skeletal muscle of bovine ~day 105 fetuses conceived by AI and ART.
Sample: Control_#4 Muscle
SAMN30890256 • SRS15142715 • All experiments • All runs
Library:
Name: GSM6588592
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Total RNA was isolated using TRIzol™ Reagent (Invitrogen, 15596026) following the manufacturer's instructions. The concentration of RNA samples was measured by using the NanoDrop® ND-1000 Spectrophotometer. RNA samples were stored at -80°C. This RNA-seq was conducted by Novogene (Sacramento, CA, USA). Briefly, total RNA samples were shipped on dry ice to Novogene overnight. Quality controls were performed for all samples using agarose gel electrophoresis to test RNA degradation and potential contamination and using Agilent 2100 Bioanalyzer to check RNA integrity and quantitation. All samples showed RNA integrity numbers (RIN) of 7.5 to 9.1 and passed the quality control. For strand specific sequencing library preparation, mRNA was enriched using oligo(dT) beads and fragmented randomly using fragmentation buffer. cDNA was synthesized by using mRNA template and random hexamers primer, after which a custom second-strand synthesis buffer (Illumina), dNTPs (dUTP instead of dTTP), RNase H and DNA polymerase I were added to initiate the second-strand synthesis. Then, double-stranded cDNA was subjected to terminal repair, 3' adenylation, sequencing adaptor ligation, uracil-DNA glycosylase degradation, size selection for 250-300bp insert, and PCR enrichment. Quality controls were performed for all libraries including Qubit concentration measurement, testing insert size using Agilent 2100 Bioanalyzer, and quantifying effective concentration using qPCR. Qualified libraries were pooled and sequenced on Illumina HiSeq platform for 150bp paired end reads.
Runs: 2 runs, 42.4M spots, 12.7G bases, 5.1Gb
Run# of Spots# of BasesSizePublished
SRR2160508533,798,99910.1G4Gb2022-11-15
SRR216050868,562,2642.6G1Gb2022-11-15

ID:
24492142

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