NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE21749 Query DataSets for GSE21749
Status Public on May 08, 2010
Title The ubiquitin-conjugating enzyme HR6B is required for maintenance of X chromosome silencing in mouse spermatocytes and spermatids
Organism Mus musculus
Experiment type Expression profiling by array
Summary Background: The ubiquitin-conjugating enzyme HR6B is required for spermatogenesis in mouse. Loss of HR6B results in aberrant histone modification patterns on the trancriptionally silenced X and Y chromosomes (XY body) and on centromeric chromatin in meiotic prophase. We studied the relationship between these chromatin modifications and their effects on global gene expression patterns, in spermatocytes and spermatids.

Results: HR6B is enriched on the XY body and on centromeric regions in pachytene spermatocytes. Global gene expression analyses revealed that spermatid-specific single- and multicopy X-linked genes are prematurely expressed in Hr6b knockout spermatocytes. Very few other differences in gene expression were observed in these cells, except for upregulation of major satellite repeat transcription. In contrast, in Hr6b knockout spermatids, 7298 genes were differentially expressed; 65% of these genes was downregulated, but we observed a global upregulation of gene transcription from the X chromosome. In wildtype spermatids, approximately 20% of the single-copy X-linked genes reach an average expression level that is similar to the average expression from autosomes.

Conclusions: Spermatids maintain an enrichment of repressive chromatin marks on the X chromosome, originating from meiotic prophase, but this does not interfere with transcription of the single-copy X-linked genes that are reactivated or specifically activated in spermatids. HR6B represses major satellite repeat transcription in spermatocytes, and functions in the maintenance of X chromosome silencing in spermatocytes and spermatids. It is discussed that these functions involve modification of chromatin structure, possibly including H2B ubiquitylation.
 
Overall design 8 Affymetrix microarrays were generated: 4 from wildtype and HR6B knockout spermatocytes (2 replicates each), and 4 from wildtype and HR6B knockout spermatids (2 replicates each).
 
Contributor(s) Achame EM, Wassenaar E, Hoogerbrugge JW, Sleddens-Linkels E, Ooms M, Sun Z, van IJcken WF, Grootegoed JA, Baarends WM
Citation(s) 20537150
Submission date May 07, 2010
Last update date Feb 11, 2019
Contact name Eskeatnaf Mulugeta Achame
E-mail(s) e.mulugetaachame@erasmusmc.nl
Phone 0031614883537
URL http://www.erasmusmc.nl/rede/
Organization name Erasmusmc
Department Reproduction and Development
Lab Reproduction and Development
Street address Dr Molewaterplein 50
City Rotterdam
State/province Rotterdam
ZIP/Postal code 3015 GE
Country Netherlands
 
Platforms (1)
GPL1261 [Mouse430_2] Affymetrix Mouse Genome 430 2.0 Array
Samples (8)
GSM542304 Late Spermatocyte, HR6B Knockout, rep1
GSM542305 Late Spermatocyte, HR6B Knockout, rep2
GSM542306 Late Spermatocyte, Wildtype, rep1
Relations
BioProject PRJNA127337

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
GSE21749_RAW.tar 29.9 Mb (http)(custom) TAR (of CEL)
Raw data provided as supplementary file
Processed data included within Sample table

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