NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE128566 Query DataSets for GSE128566
Status Public on Sep 05, 2019
Title X chromosome domain architecture regulates Caenorhabditis elegans lifespan but not dosage compensation [RNA-seq]
Organism Caenorhabditis elegans
Experiment type Expression profiling by high throughput sequencing
Summary Mechanisms establishing higher-order chromosome structures and their roles in gene regulation are elusive. We analyzed chromosome architecture during nematode X-chromosome dosage compensation, which represses transcription via a dosage-compensation condensin complex (DCC) that binds hermaphrodite Xs and establishes megabase-size topologically associating domains (TADs). We show that DCC binding at high-occupancy sites (rex sites) defines eight TAD boundary locations. Single rex deletions disrupted boundaries, and single insertions created new boundaries, demonstrating one rex site is necessary and sufficient for DCC-dependent boundary formation. Deleting eight rex sites (8rexΔ) recapitulated TAD structure of DCC mutants, permitting analysis when chromosome-wide domain architecture was disrupted but most DCC binding remained. 8rexΔ animals exhibited no changes in X expression and lacked dosage-compensation mutant phenotypes. Hence, TAD boundaries are neither the cause nor consequence of gene repression during dosage compensation. Abrogating TAD structure did, however, reduce thermotolerance, accelerate aging, and shorten lifespan, implicating chromosome architecture in regulating stress responses and aging.
 
Overall design We performed in RNA-seq on five replicates of wild-type and 8rexΔ embryos and three replicates of DCC mutant embryos. For each replicate, worms were grown and embryos collected for all genotypes in parallel. Gene expression in 8rexΔ and DCC mutant is compared to wild-type expression.
 
Contributor(s) Anderson EC, Frankino PA, Higuchi-Sanabria R, Yang Q, Bian Q, Podshivolova K, Shin A, Kenyon C, Dillin A, Meyer BJ
Citation(s) 31491396
Submission date Mar 19, 2019
Last update date Dec 05, 2019
Contact name Elphege P Nora
E-mail(s) elphege.nora@ucsf.edu
Organization name UCSF
Department CVRI
Lab Nora
Street address 555 Mission Bay Blvd S
City San Francisco
State/province CA
ZIP/Postal code 94158
Country USA
 
Platforms (1)
GPL22765 Illumina HiSeq 4000 (Caenorhabditis elegans)
Samples (3)
GSM3680236 WT_RNA-seq
GSM3680237 8rexDeletion_RNA-seq
GSM3680238 DCCmutant_RNA-seq
This SubSeries is part of SuperSeries:
GSE128568 X chromosome domain architecture regulates Caenorhabditis elegans lifespan but not dosage compensation
Relations
BioProject PRJNA528111
SRA SRP188887

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE128566_WT_8rexDeletion_DCCmutant_RNAseq.txt.gz 884.2 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap