Metabolomics,Unknown,Transcriptomics,Genomics,Proteomics

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Purification and transcriptomic analysis of mouse fetal Leydig cells reveals candidate genes for disorders of sex development


ABSTRACT: To examine the transcriptome of early testicular somatic cells during gonadogenesis at 12.5dpc RNA sequencing (RNA-Seq) was performed on murine primary testicular cell lineages isolated from the Sf1-eGFP line by FACS. The three main somatic cell lineages of the testis were isolated: the Sertoli cells which direct male development; the fetal Leydig cells (FLCs) that produce steroid hormones and virilise the XY individual and a heterogenous population of interstitial cells, some of which give rise to the adult Leydig cells (ALCs). This dataset provides a platform for exploring the biology of FLCs and understanding the role of these cells in testicular development and masculinization of the embryo, and a basis for targeted studies designed to identify causes of idiopathic XY DSD. RNA-Seq of 3 enriched cell populations from 12.5dpc mouse gonad (Sertoli cells, Leydig cells and Interstitial cells isolated by FACS-sorting) on an Illumina HiSeq 1500, in triplicate.

ORGANISM(S): Mus musculus

SUBMITTER: Katrina Bell 

PROVIDER: E-GEOD-65498 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Purification and Transcriptomic Analysis of Mouse Fetal Leydig Cells Reveals Candidate Genes for Specification of Gonadal Steroidogenic Cells.

McClelland Kathryn S KS   Bell Katrina K   Larney Christian C   Harley Vincent R VR   Sinclair Andrew H AH   Oshlack Alicia A   Koopman Peter P   Bowles Josephine J  

Biology of reproduction 20150408 6


Male sex determination hinges on the development of testes in the embryo, beginning with the differentiation of Sertoli cells under the influence of the Y-linked gene SRY. Sertoli cells then orchestrate fetal testis formation including the specification of fetal Leydig cells (FLCs) that produce steroid hormones to direct virilization of the XY embryo. As the majority of XY disorders of sex development (DSDs) remain unexplained at the molecular genetic level, we reasoned that genes involved in FL  ...[more]

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