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Cited by 183

The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

Disrupted gonadogenesis and male-to-female sex reversal in Pod1 knockout mice

Cui, Shiying, Ross, Andrea, Stallings, Nancy, Parker, Keith L., Capel, Blanche, Quaggin, Susan E.·2004·Development

Abstract

Congenital defects in genital and/or gonadal development occur in 1 in 1000 humans, but the molecular basis for these defects in most cases remains undefined. We show that the basic helix-loop-helix transcription factor Pod1(capsulin/epicardin/Tcf21) is essential for normal development of the testes and ovaries, and hence for sexual differentiation. The gonads of Pod1knockout (KO) mice were markedly hypoplastic, and the urogenital tracts of both XX and XY mice remained indistinguishable throughout embryogenesis. Within Pod1 KO gonads, the number of cells expressing the cholesterol side-chain cleavage enzyme (Scc) was increased markedly. Biochemical and genetic approaches demonstrated that Pod1 transcriptionally represses steroidogenic factor 1 (Sf1/Nr5a1/Ad4BP), an orphan nuclear receptor that regulates the expression of multiple genes (including Scc) that mediate sexual differentiation. Our results establish that Pod1 is essential for gonadal development, and place it in a transcriptional network that orchestrates cell fate decisions in gonadal progenitors.

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Metadata

Authors
Cui, S., Ross, A., Stallings, N., Parker, K. L., Capel, B., & Quaggin, S. E.
Venue
Development
Published
2004-08-15
Volume
131
Issue
16
Pages
4095-4105
ISSN
  • 0950-1991 (ISSN-L)
  • 1477-9129
OpenAlex
W2060004978
Cited by
183
References
4
FWCI
4.71
Type
journal article
Language
en
Open access
closed

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