Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/8297
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Type: Journal article
Title: Chorionic gonadotrophin b subunit mRNA but not luteinising hormone b subunit mRNA is expressed in the pituitary of the common marmoset (Callithrix jacchus)
Author: Muller, T.
Simoni, M.
Pekel, E.
Luetjens, C.
Chandolia, R.
Amato, F.
Norman, R.
Gromoll, J.
Citation: Journal of Molecular Endocrinology, 2004; 32(1):115-128
Publisher: Soc Endocrinology
Issue Date: 2004
ISSN: 0952-5041
1479-6813
Statement of
Responsibility: 
T. Muller, M. Simoni, E. Pekel, C.M. Luetjens, R. Chandolia, F. Amato, R.J. Norman and J. Gromoll
Abstract: The pituitary gonadotrophins LH and FSH are responsible for regulation of gametogenesis in the testis and ovary. Chorionic gonadotrophin (CG), a third closely related glycoprotein hormone derived by gene duplication of the LHbeta gene and secreted by the placenta in primates, is essential for the rescue of the corpus luteum and maintenance of pregnancy. We have recently shown that marmoset (m) CGbeta mRNA is highly expressed in the pituitary of the common marmoset (Callithrix jacchus) and that LH is less active than human CG in activating the human LH receptor lacking exon 10. To investigate further which gonadotrophin is the actual ligand of the LH receptor (LHR) of the marmoset monkey that naturally lacks exon 10, we identified and characterised the genomic organisation of the mLHbeta gene and its expression. Intergenic PCR amplification of the region encompassing the mLHbeta and the mCGbeta genes revealed that, surprisingly, mCGbeta is located 20 kbp upstream of the LHbeta gene, whereas in other species the intergenic distance is approximately 2-3 kbp. Sequence analysis of the mLHbeta coding region showed 70% identity to mCGbeta and 90% identity to human LHbeta at the amino acid level. Both gonadotrophin beta subunits are present at the genomic level, but RT-PCR of pituitary and placental total RNA using specific oligonucleotides for mCGbeta and mLHbeta showed high expression of mCGbeta mRNA in both tissues, whereas LHbeta was expressed neither in the pituitary nor in the placenta. Thus mLHbeta mRNA is lacking in the marmoset pituitary. Immunohistochemistry of marmoset pituitaries showed that mCG was confined to the gonadotrophes, and partly co-localised in cells stained positively for FSH. Western blot analysis confirmed the presence of mCG in the pituitary. Northern blot analysis using mCGbeta as a probe displayed one transcript of 0.7 kb in the pituitary and detected two transcripts of 1.1 kb and 2 kb in the marmoset placenta. Our results suggest that, in the common marmoset, CG is the only gonadotrophin with luteinising function that is present in the pituitary. We postulate that, owing to an unknown mutational event in evolution, expression of mLH was completely abolished, and CG - which, unlike LH, acts normally even when exon 10 is missing from the LHR - took over its function.
Keywords: Pituitary Gland; Placenta; Animals; Callithrix; Humans; Chorionic Gonadotropin, beta Subunit, Human; Follicle Stimulating Hormone; Luteinizing Hormone, beta Subunit; Receptors, LH; RNA, Messenger; Reverse Transcriptase Polymerase Chain Reaction; Amino Acid Sequence; Exons; Molecular Sequence Data
Description: Copyright © 2004 by Society for Endocrinology
RMID: 0020040264
DOI: 10.1677/jme.0.0320115
Appears in Collections:Obstetrics and Gynaecology publications

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