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Series GSE104850 Query DataSets for GSE104850
Status Public on Apr 27, 2018
Title Interrogating the functions of PRDM9 domains in meiosis
Organism Mus musculus
Experiment type Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Non-coding RNA profiling by high throughput sequencing
Summary Homologous recombination is required for proper segregation of homologous chromosomes during meiosis. It predominantly occurs at recombination hotspots that are defined by the DNA binding specificity of the PRDM9 protein. PRDM9 contains three domains which are typically different families of proteins involved in regulation of transcription in other proteins, yet, the role of PRDM9 in gene expression control has not been evaluated. Here we analyze the germline transcriptome of the  Prdm9-/- male mice in comparison to Prdm9+/+ males and find no apparent differences in the mRNA and miRNA profiles. We further explore the role of PRDM9 in meiosis by analyzing the activity of PRDM9 lacking effect of the KRAB, SSXRD and post-SET zinc finger domains deletion mutants in a cell expression system and the KRAB domain deletion in mice. We found that although the post-SET zinc finger and the KRAB domains are not essential for the methyltransferase activity of PRDM9 in a cell culture expression systemin vitro, mice lacking the KRAB domain mutant mice  domain show only residual PRDM9 methyltransferase activity and undergo meiotic arrest. In aggregate, our data indicate that these domains that are classically involved in gene regulation do not serve that role in PRDM9, but instead are involved in PRDM9 function has likely diverged from the typical function of a transcription factor and adapted the new role in setting the proper chromatin environment for initiation and completion of homologous recombination.
 
Overall design Testes mRNA-seq, miRNA-seq, Chip-seq were generated using next generation sequencing.

* The "GSE104850_RAW.tar" archive includes the processed data files for Samples GSM3053281-GSM3053299. *
 
Contributor(s) Thibault-Sennett S, Yu Q, Smagulova F, Cloutier J, Brick K, Camerini-Otero D, Petukhova GV
Citation(s) 29674518
Submission date Oct 11, 2017
Last update date Mar 25, 2019
Contact name Galina Petukhova
E-mail(s) galina.petukhova@usuhs.edu
Organization name USUHS
Department Biochemistry
Street address 4301 Jones Bridge Rd
City Bethesda
State/province Maryland
ZIP/Postal code 20814
Country USA
 
Platforms (2)
GPL17021 Illumina HiSeq 2500 (Mus musculus)
GPL19057 Illumina NextSeq 500 (Mus musculus)
Samples (28)
GSM3053272 mRNA-seq Prdm9-/- #1
GSM3053273 mRNA-seq Prdm9-/- #2
GSM3053274 mRNA-seq Hop2-/- #1
Relations
BioProject PRJNA413989
SRA SRP119794

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
GSE104850_RAW.tar 1.7 Gb (http)(custom) TAR (of BED, BIGWIG)
GSE104850_RNA-seq_TPM_genes.csv.gz 1.4 Mb (ftp)(http) CSV
GSE104850_RNA-seq_TPM_transcripts.csv.gz 4.7 Mb (ftp)(http) CSV
GSE104850_RNA-seq_ens_gene_sleuth.csv.gz 1.5 Mb (ftp)(http) CSV
GSE104850_miRNA_DEseq2_result.csv.gz 89.0 Kb (ftp)(http) CSV
GSE104850_microRNA-seq_TPM_annotated_miRNA.csv.gz 24.8 Kb (ftp)(http) CSV
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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