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Series GSE25222 Query DataSets for GSE25222
Status Public on Nov 10, 2010
Title Suppression of insulin like3 receptor reveals the role of β-catenin and Notch signaling in gubernaculum development
Organism Mus musculus
Experiment type Expression profiling by array
Summary During male development, the testes move from a high intraabdominal position and descend into the scrotum. The gubernaculum, an inguinoscrotal ligament connecting the testis to the lower abdomen, is believed to play a critical role in this process. The first stage of testicular descent is controlled by INSL3, insulin like3 hormone, produced in testicular Leydig cells. Deletion of Insl3 or its receptor, Rxfp2, in mice causes cryptorchidism. We produced Cre/loxP regulated shRNA transgenic mice targeting RXFP2 expression. We have shown that the transgene was able to reduce Rxfp2 gene expression and thus behaved as a hypomorphic allele of Rxfp2. Variable degrees of uni-and bilateral cryptorchidism was detected in males with the activated shRNA transgene on an Rxfp2+/- background. Conditional suppression of Rxfp2 in the gubernaculum led to cryptorchidism. Gene expression analysis of a mutant cremasteric sac using Illumina microarrays indicated abnormal expression of a significant number of genes in Wnt/β-catenin and Notch pathways. We have demonstrated profound changes in the expression pattern of β-catenin, Notch1, desmin, and androgen receptor (AR) in Rxfp2-/- male embryos, indicating the role of INSL3 in proliferation, differentiation, and survival of specific cellular components of the gubernaculum. We have shown that INSL3/RXFP2 signaling is essential for myogenic differentiation and maintenance of AR-positive cells in the gubernaculum. Males with the deletion of β-catenin or Notch1 in the gubernacular ligament demonstrated abnormal development. Our data indicates that β-catenin and Notch pathways are potential targets of INSL3 signaling during gubernacular development.
 
Overall design Total RNA obtained from the cremasteric sac of cryptorchid Tg(shRxfp1) males compared to the wild-type control cremasteric sac.
 
Contributor(s) Agoulnik A
Citation(s) 21147849
Submission date Nov 09, 2010
Last update date Jan 16, 2019
Contact name Alexander I Agoulnik
E-mail(s) aagoulni@fiu.edu
Organization name Florida International University
Department Herbert Wertheim College of Medicine
Street address 11200 SW 8th Street, HLSI 419B
City Miami
State/province FL
ZIP/Postal code 33199
Country USA
 
Platforms (1)
GPL6887 Illumina MouseWG-6 v2.0 expression beadchip
Samples (6)
GSM620805 Wild-type cremasteric sac, rep1
GSM620806 Cryptorchid cremasteric sac, rep1
GSM620807 Wild-type cremasteric sac, rep2
Relations
BioProject PRJNA134459

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
GSE25222_RAW.tar 15.8 Mb (http)(custom) TAR
GSE25222_non-normalized.txt.gz 1.9 Mb (ftp)(http) TXT
Processed data included within Sample table

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