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SRX1058768: GSM1711927: Cab12: ES d7 input CHIRT-seq; Mus musculus; OTHER
1 ILLUMINA (Illumina HiSeq 2000) run: 37.1M spots, 3.7G bases, 2.3Gb downloads

Submitted by: NCBI (GEO)
Study: PAR-TERRA RNA directs homologous sex chromosome pairing
show Abstracthide Abstract
In mammals, homologous chromosomes rarely pair outside meiosis. One exception is the X chromosome, which transiently pairs during X-chromosome inactivation (XCI). How two chromosomes find each other in 3D space is not known. Here, we reveal a required interaction between the X-inactivation center (Xic) and the telomere in mouse embryonic stem (ES) cells. The subtelomeric, pseudoautosomal regions (PARs) of the two sex chromosomes (X and Y) also undergo pairing in both female and male cells. PARs transcribe a class of telomeric RNA, dubbed PAR-TERRA, which accounts for a vast majority of all TERRA transcripts. PAR-TERRA binds throughout the genome, including to the PAR and Xic. During X-chromosome pairing, PAR-TERRA anchors the Xic to the PAR, creating a ‘tetrad’ of pairwise homologous interactions (Xic–Xic, PAR–PAR, and Xic–PAR). Xic pairing occurs within the tetrad. Depleting PAR-TERRA abrogates pairing and blocks initiation of XCI, whereas autosomal PAR-TERRA induces ectopic pairing. We propose a ‘constrained diffusion model’ in which PAR-TERRA creates an interaction hub to guide Xic homology searching during XCI. Overall design: Identify genome-wide binding sites for TERRA RNA by CHIRT-seq in ES cells and MEFs. TERRA capture RNA-seq to discover TERRA sequence. Investigation of PAR-interacting domains using 4C-Seq. Please note that GSM2429690-93 are duplicated sample records of GSM1711915-18, respectively, for the convenient retrieval of the complete raw data from SRA.
Sample: Cab12: ES d7 input CHIRT-seq
SAMN03775228 • SRS961102 • All experiments • All runs
Organism: Mus musculus
Library:
Instrument: Illumina HiSeq 2000
Strategy: OTHER
Source: GENOMIC
Selection: other
Layout: PAIRED
Construction protocol: CHIRT-seq: Nuclei were crosslinked in 1% glutaraldehyde and chromatin were sheared to 0.5~3kb. Chromatin was incubated with biotinylated capture oligonucleotides that were complementary to PAR-TERRA RNA, and the hybridized material was captured by streptavidin beads. Enriched DNA was eluted by RNaseH digestion. CHIRT-seq: Eluted genomic DNA or input samples were fragmented into a median size of 220 bp, and the sequencing libraries were constructed according to NEB ChIP-Seq library protocol.
Experiment attributes:
GEO Accession: GSM1711927
Links:
Runs: 1 run, 37.1M spots, 3.7G bases, 2.3Gb
Run# of Spots# of BasesSizePublished
SRR206298037,132,3693.7G2.3Gb2017-07-10

ID:
1535963

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