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PMID: 8058073 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Developmental expression of mouse steroidogenic factor-1, an essential regulator of the steroid hydroxylases.

Molecular endocrinology (Baltimore, Md.) ·Vol. 8 ·No. 5 ·1994-05-00 ·Pages 654-62

Ikeda Y, Shen WH, Ingraham HA, Parker KL

Abstract

As an initial step toward understanding its role in steroidogenesis, we studied the developmental profile of steroidogenic factor-1 (SF-1), a nuclear receptor that regulates the steroid hydroxylases. SF-1 transcripts first appear on embryonic day 9 (E9) in the urogenital ridge, the probable source of steroidogenic cells of both adrenals and gonads. By E11, after the adrenals and gonads are clearly separate, SF-1 transcripts are detected throughout the adrenal primordium. Thereafter, adrenal expression of SF-1 localizes to the cortex. Consistent with its proposed role in regulating cholesterol side-chain cleavage enzyme (SCC), SF-1 is expressed before SCC. During the sexually undifferentiated stage of gonadal development (E9-E12), all embryos express SF-1 in the genital ridge. As testicular cords form in males, SF-1 transcripts are diffusely expressed throughout the testis, whereas SCC mRNA is limited to the interstitium. These differences between SF-1 and SCC reflect SF-1 expression by Sertoli cells, as shown by Northern blotting and in situ hybridization. In contrast to its persistent expression in the embryonic testis, SF-1 transcripts disappear from the ovary between E13.5-E16.5, reappearing only during late gestation (E18.5). Thus, expression of SF-1 in the embryonic gonad is sexually dimorphic. Coupled with the demonstration of SF-1 mRNA in Sertoli cells, these data suggest that SF-1 plays a role in gonadal development distinct from regulating the steroidogenic enzymes. Additionally, SF-1 is expressed in the embryonic forebrain, implying a role in neural development.

MeSH Terms
Adrenal Glands/cytology,embryology,metabolism Animals Base Sequence Brain/cytology,embryology,metabolism DNA Primers DNA-Binding Proteins/biosynthesis Diencephalon/cytology,embryology,metabolism Embryonic and Fetal Development Female Fushi Tarazu Transcription Factors Gene Expression Gestational Age Homeodomain Proteins Homeostasis In Situ Hybridization Male Mice Molecular Sequence Data Ovary/cytology,embryology,metabolism Polymerase Chain Reaction/methods Prosencephalon/cytology,embryology,metabolism RNA, Messenger/analysis,biosynthesis Receptors, Cytoplasmic and Nuclear/biosynthesis Sertoli Cells/cytology,metabolism Sex Determination Analysis Steroid Hydroxylases/biosynthesis Steroidogenic Factor 1 Testis/cytology,embryology,metabolism Transcription Factors/biosynthesis Transcription, Genetic
Chemicals
DNA Primers DNA-Binding Proteins Fushi Tarazu Transcription Factors Homeodomain Proteins RNA, Messenger Receptors, Cytoplasmic and Nuclear Steroidogenic Factor 1 Transcription Factors steroidogenic factor 1, mouse Steroid Hydroxylases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Ikeda Y
Department of Medicine, Howard Hughes Medical Institute, Duke University Medical Center, Durham, North Carolina 27710.
Shen W H
Ingraham H A
Parker K L
Article Info
Journal
Molecular endocrinology (Baltimore, Md.)
Abbr.
Mol Endocrinol
ISSN
0888-8809
Published
1994-05-00
Pages
654-62
Language
English
Region
United States
NLM ID
8801431
Subset
IM
Grants
NIDDK NIH HHS · DK-46048 · United States
NICHD NIH HHS · HD-30725 · United States
NHLBI NIH HHS · HL-48460 · United States
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