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Sample GSM8216286 Query DataSets for GSM8216286
Status Public on Jun 01, 2024
Title H3K27ac, adult-rumen, 1 (chip-seq)
Sample type SRA
 
Source name Rumen
Organism Bos taurus
Characteristics tissue: Rumen
Sex: male
age: 2 years adult
genotype: WT
chip antibody: H3K27ac
Treatment protocol For pluripotent stem cells: The bovine embryonic stem cell line bESCs-F7 was established using the CTFR system. Two treatment methods were employed for bESCs-F7 using MM-102: one involved treating bESCs-F7 with a high concentration (50 μM) of MM-102 for 7 days, followed by normal culturing for 5 passages before characterization, labeled as bESCs-F7-102 (50). The other involved long-term treatment with a low concentration (5 μM) of MM-102, followed by characterization after 5 passages of culturing, labeled as bESCs-F7-102 (5). Bovine induced pluripotent stem cells and the bEPSCs-B18 cell line were established using the LCDM system. And bEPSCs-AGS was using a 500mL system, including 485mL of basic mTeSR1 medium, 5.0 mL of 100×Penicillin-Streptomycin Solution, 0.1 mM 2-mercaptoethanol, 1 μM GSK3β inhibitor CHIR99021, 0.3 μM Lck/Src inhibitor WH-4-023, 5 μM Tankyrase inhibitor XAV939, 5 μM classic WNT signaling pathway inhibitor IWR-1, 50 μg/mL Vitamin C, 10 ng/mL Leukemia Inhibitory Factor (LIF), and 20.0 ng/mL Activin A for culturing bovine Embryonic Pluripotent Stem Cells.
Growth protocol For tissues, we collected fetal tissues from four healthy pregnant Holstein cows at a slaughterhouse. After the slaughter, we extracted fetal tissues to examine their normal development and measured the crown-rump length (CRL) to estimate gestational age. The gender was identified based on the position of the gonads within the abdominal cavity, anatomical structures, and relationships with adjacent organs (mesonephros and/or kidneys). Two male and two female fetuses were identified (13-16 cm CRL), nine different tissues were collected, including the forebrain, hindbrain, heart, liver, lungs, skeletal muscle (hind limb), kidneys, rumen, and testes.
Extracted molecule genomic DNA
Extraction protocol Cells were collected by tryple-select enzyme and the lyophilized cells were sent for sequencing. The sequencing was performed by Tianjin Nuohe Zhiyuan Biotechnology Co., LTD, Tianjin, China.
The Simple ChIP®Plus Enzymatic Chromatin IP Kit (Magnetic Beads) (9005, Cell Signaling) was utilized to extract DNA fragments from the cells.
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina NovaSeq 6000
 
Data processing Illumina reads were first mapped to the UCSC bosTau9 reference using bwa-mem (version:0.7.17) with default parameters.
Next, Picard (http://broadinstitute.github.io/picard/, accessed on 12 June 2023, version 2.23.1) was used to mark up the PCR duplicates.
Then, we used macs2 (v2.2.7.1, -nomodel-broad-broad-cutoff 0.1-shift 0-gsize 2.7e9-keep-dup auto) to call the peaks.
H3K4me1 signals were normalized using the MA norm (version: 1.1.4) method for the quantitative comparison of ChIP-seq data, and the significant differential peaks were determined as log10(p-value) < 0 and M-value > 1. Subsequently, the differential peaks were annotated to UCSC bosTau9 using the R package ChIP seeker (version: 1.28.3) and TxDb.Btaurus.UCSC.bosTau9.refGene (version: 3.10.0).
Assembly: UCSC BT9
Supplementary files format and content: bigWig
 
Submission date Apr 18, 2024
Last update date Jun 01, 2024
Contact name jing wang
E-mail(s) nnlrl@mail.imu.edu.cn
Organization name Inner Mongolia University
Street address Zhaojun Road
City Hohhot
State/province Nei Mongol
ZIP/Postal code 010000
Country China
 
Platform ID GPL26012
Series (2)
GSE264336 Epigenetic Basis for the Establishment of Ruminal Tissue-Specific Functions (ChIP-seq)
GSE264346 Epigenetic Basis for the Establishment of Ruminal Tissue-Specific Functions
Relations
BioSample SAMN41008847
SRA SRX24353591

Supplementary file Size Download File type/resource
GSM8216286_adult-H3K27ac_REP1.bamCompare.bw 113.2 Mb (ftp)(http) BW
SRA Run SelectorHelp
Raw data are available in SRA

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