ONTOGENY OF LUTEINIZING-HORMONE RECEPTOR GENE-EXPRESSION IN THE RAT TESTIS

Citation
Fp. Zhang et al., ONTOGENY OF LUTEINIZING-HORMONE RECEPTOR GENE-EXPRESSION IN THE RAT TESTIS, Endocrinology, 134(5), 1994, pp. 2206-2213
Citations number
42
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
00137227
Volume
134
Issue
5
Year of publication
1994
Pages
2206 - 2213
Database
ISI
SICI code
0013-7227(1994)134:5<2206:OOLRGI>2.0.ZU;2-L
Abstract
The ontogeny of expression of the LH receptor (LHR) gene was studied i n rat testis between day 12.5 of fetal life and adulthood. Specific hy bridization of testicular mRNA with a LHR cRNA probe encoding the extr acellular domain of the receptor was found from day 16.5 of fetal life onward in Northern hybridization. Transcripts of 6.8, 4.2, and 2.7 ki lobases were present at all ages, and a 1.8-kilobase species was prese nt mainly in the adult testes. Hybridization was most intensive in day 21.5 fetuses, decreased after birth, and increased again by adulthood . The LHR mRNA was also analyzed by the reverse transcriptase-polymera se chain reaction technique, with primers multiplying either the full- length LHR mRNA or its extracellular domain. The specificity of the DN A species generated was verified by Southern hybridization using a nes ted P-32-labeled oligonucleotide. The results indicated that a truncat ed mRNA form, encoding the extracellular part of LHR, appears 1 day be fore the full-length LHR mRNA, i.e. on fetal days 14.5 and 15.5, respe ctively. This is in striking contrast to the rat fetal ovary, in which a difference of more than 10 days is found in the appearance of these two LHR mRNAs (17.5 days of fetal and 7 days of postnatal age, respec tively). The appearance of the full-length LHR mRNA coincides in both sexes with the developmental onset of LHR binding observed in earlier studies. In situ. hybridization using an antisense cRNA probe demonstr ated that the LHR mRNA was confined to Leydig cells at all fetal and p ostnatal ages studied. In conclusion, there is good correlation in the developing rat testes between the onset of LHR gene expression and LH R binding, as observed in earlier studies. The findings in the fetal t estis are at striking variance with those in the ovary, which starts e xpressing the extracellular domain of the LHR mRNA at roughly the same age as the testis. However, the appearance of full-length LHR mRNA an d the functional receptor are delayed until day 7 postpartum.