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Structure and expression of the rat relaxin‐like factor (RLF) gene
Author(s) -
Spiess AndrejNikolai,
Balvers Marga,
TenaSempere Manuel,
Huhtaniemi Ilpo,
Parry Laura,
Ivell Richard
Publication year - 1999
Publication title -
molecular reproduction and development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.745
H-Index - 105
eISSN - 1098-2795
pISSN - 1040-452X
DOI - 10.1002/(sici)1098-2795(199912)54:4<319::aid-mrd1>3.0.co;2-z
Subject(s) - biology , leydig cell , endocrinology , theca , medicine , relaxin , testosterone (patch) , gene expression , ovary , andrology , gene , hormone , luteinizing hormone , genetics
The relaxin‐like factor (RLF) is a novel member of the insulin‐IGF‐relaxin family of growth factors and hormones, and its mRNA is expressed very specifically in the Leydig cells of the testis and in the theca and luteal cells of the ovary. Here we report the cloning of the RLF gene and cDNA from the rat. The 0.8kb mRNA is produced from a small gene comprising two exons situated less than 1 kb downstream of the gene for the signalling factor JAK3. Northern hybridization confirms high RLF mRNA expression in the adult rat testis, and low expression in the ovary, but in no other tissues examined. Northern analysis of fetal and neonatal gonadal tissues showed that RLF mRNA is highly upregulated in the testes of day 19 embryos, but not in later neonatal stages, nor in any ovarian tissue from this period. This would indicate that RLF is a marker for the mature fetal as well as the adult‐type Leydig cell, but is not expressed in premature, precursor, or dedifferentiated Leydig cells of either cell type. Finally, RNA was analysed from the testes of rats which had been treated with ethylene dimethane sulfonate (EDS), an alkylating agent that specifically destroys rat Leydig cells. RLF mRNA was absent from the acutely treated testes, but became detectable between 15 and 20 days post‐treatment, concomitant with the repopulation of the testes by new Leydig cells. Continuous testosterone substitution of EDS‐treated rats suppressed the production of gonadotropins, and LH‐dependent Leydig cell differentiation, with the result that RLF mRNA remained undetectable throughout the study period. In conclusion, RLF is a very specific marker for the mature Leydig cell phenotype in both the adult‐type and fetal Leydig cell populations of the rat testis. Mol. Reprod. Dev. 54:319–325, 1999. © 1999 Wiley‐Liss, Inc.