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Series GSE199717 Query DataSets for GSE199717
Status Public on Apr 18, 2024
Title Condensin I folds the C. elegans genome [RNA-seq]
Organism Caenorhabditis elegans
Experiment type Expression profiling by high throughput sequencing
Summary Structural Maintenance of chromosomes (SMC) complexes, cohesin and condensins, have been named after their roles during meiosis and mitosis. Recent data in mammalian cells and Drosophila have described the additional role of cohesin for genome folding into loops and domains during interphase. However, determinants of genome folding in holocentric species remain unclear. Using high resolution chromosome conformation capture, we show that overlapping large-scale nuclear localization and small-scale epigenomic states compartmentalize the C. elegans genome. By systematically and acutely inactivating each SMC complex, we observe that in contrast to other studied systems, cohesin creates small loops, while condensin I has a major role in genome folding: its inactivation causes genome-wide decompaction, chromosome mixing, loss of loops and TAD structures and reinforcement of fine-scale epigenomic compartments. Counter-intuitively, removal of condensin I and its X-specific variant condensin IDC from the X chromosomes led to the formation of a loop compartment coinciding with a subset of previously characterized loading sites for condensin IDC and bound by the X-targeting complex SDC. While transcriptional changes were limited for all autosomes upon cohesin and condensin II inactivation, removal of condensin I/IDC from the X chromosome led to transcriptional up-regulation of X-linked genes demonstrating that a sustained role for condensin IDC in gene regulation. Finally, while condensin I inactivation leads to reduced lifespan, we show that this reduction is due to X-specific gene upregulation rather than global genome decompaction.
 
Overall design In this study, a total of 40 samples were analysed that comprise of 9 different strains in which different SMC complexes were inactivated and their controls. Each strain/condition has 3-4 biological replicates.
 
Contributor(s) Das M, Semple J, Scotton J, Annan A, Campos J, Meister P
Citation(s) 39039278
Submission date Mar 29, 2022
Last update date Jul 23, 2024
Contact name Peter Meister
E-mail(s) peter.meister@unibe.ch
Phone +41316844609
Organization name University of Bern
Department Institute of Cell Biology
Lab Cell Fate and Nuclear Organization
Street address Baltzerstrasse 4
City Bern
State/province Schweiz
ZIP/Postal code 3012
Country Switzerland
 
Platforms (1)
GPL26672 Illumina NovaSeq 6000 (Caenorhabditis elegans)
Samples (40)
GSM5982652 RNA-seq: TEV control replicate 1, BATCH 1
GSM5982653 RNA-seq: TEV control replicate 2, BATCH 1
GSM5982654 RNA-seq: TEV control replicate 3, BATCH 1
This SubSeries is part of SuperSeries:
GSE199723 Condensin I folds the C. elegans genome
Relations
BioProject PRJNA821226

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
GSE199717_RAW.tar 46.9 Mb (http)(custom) TAR (of SF)
GSE199717_sumFR_366_B_UniqueMultiple.bw 129.6 Mb (ftp)(http) BW
GSE199717_sumFR_366_C_UniqueMultiple.bw 139.7 Mb (ftp)(http) BW
GSE199717_sumFR_366_D_UniqueMultiple.bw 132.6 Mb (ftp)(http) BW
GSE199717_sumFR_382_B_UniqueMultiple.bw 127.3 Mb (ftp)(http) BW
GSE199717_sumFR_775_B_UniqueMultiple.bw 126.1 Mb (ftp)(http) BW
GSE199717_sumFR_784_B_UniqueMultiple.bw 130.7 Mb (ftp)(http) BW
GSE199717_sumFR_821_D_UniqueMultiple.bw 142.3 Mb (ftp)(http) BW
GSE199717_sumFR_822_A_UniqueMultiple.bw 132.8 Mb (ftp)(http) BW
GSE199717_sumFR_822_C_UniqueMultiple.bw 128.7 Mb (ftp)(http) BW
GSE199717_sumFR_823_D_UniqueMultiple.bw 145.8 Mb (ftp)(http) BW
GSE199717_sumFR_828_C_UniqueMultiple.bw 141.0 Mb (ftp)(http) BW
GSE199717_sumFR_844_C_UniqueMultiple.bw 145.9 Mb (ftp)(http) BW
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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