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PMID: 7768331 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Ontogeny of follicle-stimulating hormone receptor gene expression in the rat testis and ovary.

Molecular and cellular endocrinology ·Vol. 107 ·No. 2 ·1995-02-00 ·Pages 199-208

Rannikki AS, Zhang FP, Huhtaniemi IT

Abstract

The ontogeny of the follicle-stimulating hormone (FSH) receptor (R) gene expression was studied in the rat testis and ovary between day 12.5 or 14.5 of fetal life (f), respectively, and adulthood. In Northern blots hydbridized with a cRNA probe corresponding to a part of the extracellular domain of the FSHR, specific hybridization to testicular RNA was detected from day f18.5, and to ovarian RNA from postnatal day 7 onwards. The main transcripts in the testis were at all ages 7.0 kb and 2.5 kb in size. In the ovary, the main transcript was always 2.5 kb in size. In order to increase the sensitivity of mRNA detection, the FSHR gene expression was also analyzed using the reverse transcriptase-polymerase chain reaction (RT-PCR) technique with primer pairs corresponding to the near full-length FSHR mRNA or to its extracellular domain. The specificity of the PCR products was verified by Southern hybridization using a nested 32P-labeled cDNA probe. The results indicated that the expression of the extracellular domain of the FSHR was first detected on day f14.5 in the testis and on day f20.5 in the ovary. The full-length mRNA appeared in both sexes 2 days later, which is in agreement with earlier measurements of appearance of FSHR binding in the rat testis (day f17.5) and ovary (day 3 post partum). In situ hybridization using an antisense cRNA probe for FSHR demonstrated that, as early in development as specific hybridization was detected, it was confined to the Sertoli cells in the testis and to granulosa cells in the ovary. When compared with the developmental onset of the LHR gene expression (our earlier data), a major difference was observed in the ovary; the message encoding the extracellular LHR domain appeared > 10 days earlier than that corresponding to the full-length LHR message. In the case of mRNAs for the testicular LHR, and for FSHR of both sexes, the difference between the developmental appearance of the truncated and full-length RNA forms was only 2 days.

Related Genes
MeSH Terms
Animals Base Sequence DNA Primers/genetics Female Gene Expression Regulation, Developmental In Situ Hybridization Male Molecular Sequence Data Ovary/embryology,growth & development,metabolism Polymerase Chain Reaction RNA, Messenger/genetics,metabolism Rats Rats, Sprague-Dawley Receptors, FSH/genetics Testis/embryology,growth & development,metabolism
Chemicals
DNA Primers RNA, Messenger Receptors, FSH
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Rannikki A S
Department of Physiology, University of Turku, Finland.
Zhang F P
Huhtaniemi I T
Article Info
Journal
Molecular and cellular endocrinology
Abbr.
Mol Cell Endocrinol
ISSN
0303-7207
Published
1995-02-00
Pages
199-208
Language
English
Region
Ireland
NLM ID
7500844
Subset
IM
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