Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Histone
Antigen
H3K9me3

Cell type

Cell type Class
Gonad
Cell type
Spermatocytes
MeSH Description
Male germ cells derived from SPERMATOGONIA. The euploid primary spermatocytes undergo MEIOSIS and give rise to the haploid secondary spermatocytes which in turn give rise to SPERMATIDS.

Attributes by original data submitter

Sample

source_name
H3K9me3_ChIP_WT
strain
C57BL/6
Sex
male
genotype/variation
wildtype
tissue
testis
cell type
pachytene spermatocytes
chip antibody
H3K9me3 antibody (Active Motif, Cat.# 39161)

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
RNA-seq: total RNA was extracted from 500 pachytene cells using RNAqueous-Micro Total RNA Isolation Kit (ThermoFisher, AM1931) and eluted in 10 µl of elution solution. ChIP-seq: wildtype (3268 cells) and Setdb1 cKO (5203 cells) pachytene cells were used for library prep described below. RNA-seq: cDNA was amplified from 1 µl of total RNA by using Smart-seq2 protocol (S. Picelli et al., Nat Methods. 10, 1096-8. 2013; 15 amplification cycles). 10 ng of cDNA was sheared using Covaris E220. Libraries of ~300 bp were generated using Ovation Ultralow DR kit (NuGEN, 0330) with 14 PCR cycles. ChIP-seq: Ultra-low-input native ChIP-seq library was prepared by following a published protocol (J. Brind'Amour et al., Nat. Commun. 6, 6033. 2015). 5% of the samples after micrococcal nuclease digestion were taken as input. 6.25 µl of diluted H3K9me3 antibody (1:100; Active Motif, 39161) per reaction was used for ChIP. NEBNext Adapter for Illumina was used as adapters and adapter-ligated DNAs were amplified by 13 PCR cycles using NEBNext Index primers (New England Biolabs, included in E7335 and E7500). The libraries were size-selected (200-500 bp) using E-Gel (ThermoFisher).

Sequencing Platform

instrument_model
Illumina HiSeq 2500

mm10

Number of total reads
88166304
Reads aligned (%)
96.1
Duplicates removed (%)
53.4
Number of peaks
627 (qval < 1E-05)

mm9

Number of total reads
88166304
Reads aligned (%)
95.8
Duplicates removed (%)
53.4
Number of peaks
685 (qval < 1E-05)

Base call quality data from DBCLS SRA