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Series GSE196736 Query DataSets for GSE196736
Status Public on Feb 23, 2022
Title N6-methyladenosine-modified circRNA in the bovine mammary epithelial cells injured by Staphylococcus aureus and Escherichia coli
Organism Bos taurus
Experiment type Non-coding RNA profiling by high throughput sequencing
Methylation profiling by high throughput sequencing
Summary Mastitis is a common disease that hinders the development of dairy industry and animal husbandry. It leads to the abuse of antibiotics, the emergence of super drug-resistant bacteria, and poses a great threat to human food health and safety. Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) are the most common pathogens of mastitis in dairy cows and usually cause subclinical or clinical mastitis. CircRNAs and N6-methyladenosine (m6A) play important roles in immunological diseases. However, the mechanisms by which m6A modifies circRNA in bovine mammary epithelial cells remain poorly understood. The aim of our study was to investigate m6A-modified circRNAs in bovine mammary epithelial cells (MAC-T cells) injured by S. aureus and E. coli. The profile of m6A-modified circRNA showed a total of 1599 m6A peaks within 1035 circRNAs in the control group, 35 peaks within 32 circRNAs in the S. aureus group, and 1016 peaks within 728 circRNAs in the E. coli group. Compared with the control group, 67 peaks within 63 circRNAs were significantly different in the S. aureus group, and 192 peaks within 137 circRNAs were significantly different in the E. coli group. Furthermore, we found the source genes of these differentially m6A-modified circRNAs in the S. aureus and E. coli groups with similar functions according to GO and KEGG analyses, which were mainly associated with cells injury, such as inflammation, apoptosis, and autophagy. CircRNA-miRNA-mRNA interaction networks predicted the potential circRNA regulation mechanism in S. aureus- and E. coli-induced cell injury. We found that the mRNAs in the networks, such as BCL2, MIF and TNFAIP8L2, greatly participated in the MAPK, WNT, and inflammation pathways. This is the first report on m6A-modified circRNA regulation of cells under S. aureus and E. coli treatment, and sheds new light on potential mechanisms and targets from the perspective of epigenetic modification in mastitis and other inflammatory diseases.
 
Overall design Examining 3 conditions, each with 3 replicates
 
Citation(s) 35444650
Submission date Feb 15, 2022
Last update date May 25, 2022
Contact name Changmin Hu
E-mail(s) hcm@mail.hzau.edu.cn
Phone 15327197602
Organization name Huazhong Agricultural University
Street address No.1 Shizishan Street
City Wuhan
State/province Hubei
ZIP/Postal code 430070
Country China
 
Platforms (1)
GPL15749 Illumina HiSeq 2000 (Bos taurus)
Samples (18)
GSM5899948 MAC-T cells, C1.Input
GSM5899949 MAC-T cells, C1.IP
GSM5899950 MAC-T cells, C2.Input
Relations
BioProject PRJNA807131

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Supplementary file Size Download File type/resource
GSE196736_C1.circRNA.m6A.bed.gz 22.0 Kb (ftp)(http) BED
GSE196736_C2.circRNA.m6A.bed.gz 18.6 Kb (ftp)(http) BED
GSE196736_C3.circRNA.m6A.bed.gz 20.0 Kb (ftp)(http) BED
GSE196736_CircRNA_Expression_Profiling.xlsx 534.0 Kb (ftp)(http) XLSX
GSE196736_E1.circRNA.m6A.bed.gz 11.0 Kb (ftp)(http) BED
GSE196736_E2.circRNA.m6A.bed.gz 14.4 Kb (ftp)(http) BED
GSE196736_E3.circRNA.m6A.bed.gz 10.9 Kb (ftp)(http) BED
GSE196736_Methylated_RNA_sites.circRNA.xlsx 531.9 Kb (ftp)(http) XLSX
GSE196736_S1.circRNA.m6A.bed.gz 566 b (ftp)(http) BED
GSE196736_S2.circRNA.m6A.bed.gz 539 b (ftp)(http) BED
GSE196736_S3.circRNA.m6A.bed.gz 556 b (ftp)(http) BED
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