Abstract
The glycoprotein hormone family is composed of four structurally related polypeptide hormones primarily produced by two specific endocrine tissues. Three such hormones, thyrotropin (TSH), lutropin (LH), and follitropin (FSH), are produced in the anterior pituitary gland in most mammals. A fourth hormone, chorionic gonadotropin (CG), is produced by the placenta in primates and possibly other mammals (1). In addition, it is well known that CG is produced by trophoblastic and nontrophoblastic tumors (2). In particular, malignant conditions of the lung, breast, gastrointestinal system, and central nervous system may produce CG or its components, which therefore serve as possible cancer markers (3–5). Also, recent reports suggest that pituitary glycoprotein hormones may be produced in the central nervous system (6,7).
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Pierce J. G. and Parsons T. F. (1981) Glycoprotein hormones: structure and function. Ann. Rev. Biochem. 50, 465–495.
Hussa R. O. (1980) Biosynthesis of human chorionic gonadotropin. Endocr. Rev. 1, 268–294.
Borkowski A. and Muquardt C. (1979) Human chorionic gonadotropin in plasma of normal, non-pregnant subjects. N. Eng. J. Med. 301, 298–302.
Braunstein G. D., Rasor J., and Wade M. E. (1975) Presence in normal human testes of a chorionic gonadotropin-like substance distinct from human luteinizing hormone. N. Eng. J. Med. 292, 1339–1343.
Braunstein G. D., Vaitukaitis J. L., Carbone P. P., and G. T. Ross (1973) Ectopic production of human chorionic gonadotropin by neoplasms. Ann. Intern. Med. 78, 39–45.
Emanuele N. V., Anderson J., Anderson E., Connick E., Baker G., Kirsteins L., and Lawrence A. M. (1983) Extra-hypothalamic brain luteinizing hormone: Characterization by radioimmunoassay, chromatography, radioligand assay and bioassay. NeuroEndocrinology 36, 254–260.
Hojvat S., Baker G., Kirsteins L., and Lawrence A. M. (1982) TSH in the rat and monkey brain: Distribution, characterization and effect of hypophysectomy. NeuroEndocrinology 34, 327–332.
Hershman J. M. and Pekary A. E. (1985) Regulation of Thyrotropin Secretion, in The Pituitary Gland ( Imura H., ed.), Raven, New York.
Vaitukaitis J. L., Ross G. T., Braunstein G. D., and Rayford P. L. (1976) Gonadotropins and their subunits: Basic and clinical studies. Recent Prog. Horn. Res. 32, 289–331.
Vaitukaitis J. L. (1974) Changing placental concentrations of human chorionic gonadotropin and its subunits during gestation. J. Clin. Endocrinol. Metab. 38, 755–760.
Surks M. I. and Lifschitz B. M. (1977) Biphasic thyrotropin suppression in euthyroid and hypothyroid rats. Endocrinology 101, 769–781.
Chappel S. C., Ulloa-Aguirre A., and Coutifaris C. (1983) Biosynthesis and secretion of follicle-stimulating hormone. Endocr. Rev. 4, 179–211.
Clayton R. N. and Catt K. J. (1981) Gonadotropin-releasing hormone receptors: Characterization, physiological regulation, and relationship to reproductive function. Endocr. Rev. 2, 186–209.
Pierce J. G., Faith M. R., Giudice L. C., and Reeve J. R. (1976) Structure and structure-function relationships in glycoprotein hormones. Ciba Found. Symp. 41, 225–250.
Acher R. (1980) Molecular evolution of biologically active polypeptides. Proc. R. Soc. Lond. 200, 21–43.
Stewart M. and Stewart F. (1977) Constant and variable regions in glycoprotein beta subunit sequences: Implications for receptor binding specificity. J. Mol. Biol. 116, 175–179.
Godine J. E., Chin W. W., and Habener J. F. (1982) α-Subunit of rat pituitary glycoprotein hormones: Primary structure of the precursor determined from the nucleotide sequence of cloned cDNAs. J. Biol. Chem. 257, 8368–8371.
Daniels-McQueen S., McWilliams D., Birken S., Canfield R; Landefeld T., and Boime I. (1978) Identification of the mRNAs encoding the α and β subunits of human choriogonadotropin. J. Biol. Chem. 253, 7109–7114.
Chin W. W., Habener J. F., Kieffer J. D., and Maloof F. (1978) Cell- free translation of the messenger RNA coding for the α-subunit. J. Biol. Chem. 253, 7985–7988.
Vamvakopoulos N. C. and Kourides I. A. (1979) Identification of separate mRNAs coding for the α and β subunits of thyrotropin. Proc. Natl. Acad. Sci. USA 76, 3809–3813.
Godine J. E., Chin W. W., and Habener J. F. (1980) Luteinizing and follicle-stimulating hormones: Cell-free translations of mRNAs coding for subunit precursors. J. Biol. Chem. 255, 8780–8783.
Godine J. F. Chin W. W., and Habener J. F. (1981) Cell-free synthesis and processing of the precursors to the subunits of luteinizing hormone. J. Biol. Chem. 256, 2475–2479.
Alexander D. C. and Miller W. L. (1981) mRNA for ovine follicle- stimulating hormone β-chain: An in vitro ovine translation assay. J. Biol. Chem. 256, 12628–12631.
Ruddon R. W., Bryan A. H., Hanson C. A., Perini F., Ceccorulli L. M., and Peters B. P. (1981) Characterization of the intracellular and secreted forms of the glycoprotein hormone chorionic gonadotropin produced by malignant cells. J. Biol. Chem. 256, 5189–5196.
Chin W. W., Maloof F., and Habener J. F. (1981) Thyroid- stimulating hormone biosynthesis: Cellular processing, assembly, and release of subunits. J. Biol. Chem. 256, 3059–3066.
Weintraub B. D., Stannard B. S., Linnekin D., and Marshall M. (1980) Relationship of glycosylation to de novo thyroid-stimulating hormone biosynthesis and secretion by mouse pituitary tumor cells. J. Biol. Chem. 255, 5715–5723.
Giudice L. C. and Weintraub B. D. (1979) Evidence for conformational differences between precursor and processed forms of thyroid-stimulating hormone β-subunit. J. Biol. Chem. 254, 12679–12683.
Magner J. A. and Weintraub B. D. (1982) Thyroid-stimulating hormone (TSH) subunit processing and combination in microsomal subtractions of mouse pituitary tumor. J. Biol. Chem. 257, 6709–6715.
Hoshina H. and Boime I. (1982) Combination of rat lutropin subunits occurs earlv in the secretory pathway. Proc. Natl. Acad. Sci. USA 79, 7649–7653.
Van Hall E. V., Vaitukaitis J. L., Ross G. T., Hickman J. W., and Ashwell G. (1971) Immunological and biological activity of hCG following progressive desialylation. Endocrinology 88, 456–464.
Farquhar M. G. (1983) Multiple pathways of exocytosis, endocytosis, and membrane recycling: Validation of a Golgi route. Fed. Proc. 42, 2407–2413.
Blackman M. R., Gershengorn M. C., and Weintraub B. D. (1978) Excess production of free alpha subunits by mouse pituitary thyrotropic tumor cells in vitro. Endocrinology 102, 499–508.
Chin W. W., Maloof F., Martorana M. A., Pierce J. G., and Ridgway, E. C. (1981) Production and release of thyrotropin and its subunits by monolayer cultures containing bovine anterior pituitary cells. Endocrinology 108, 387–394.
Chin W. W., Habener J. F., Martorana M., Keutmann H. T., Kieffer J. D., and Maloof F. (1980) Thyroid-stimulating hormone: Isolation and partial characterization of hormone and subunits from a mouse thyrotrope tumor. Endocrinology 107, 1384–1392.
Weintraub B. D., Krauth G., Rosen S. W., and Rabson A. S. (1975) Difference between purified ectopic and normal alpha subunits of human glycoprotein hormones. J. Clin. Invest. 56, 1043–1052.
Benveniste R., Linder J., and Rabin D. (1979) Human chorionic gonadotropin alpha-subunit from cultured choriocarcinoma (JFG) cells; Comparisons of the subunit secreted free with that prepared from secreted human chorionic gonadotropin. Endocrinology 105, 581–587.
Parsons T. H., Bloomfield G. A., and Pierce J. G. (1983) Purification of an alternate form of the α subunit of the glycoprotein hormones from bovine pituitaries and identification of its O-linked oligosaccharide. J. Biol. Chem. 258, 240–244.
Parsons T. H. and Pierce J. G. (1983) Free s-like material from bovine pituitaries: Restoration of the ability to reassociate with native LH-p. Fed. Proc. 42, 1799.
Cole L. A., Hartle R. J., Laferla J. J., and Ruddon R. W. (1983) Detection of the free beta subunit of human chorionic gonadotropin (hCG) in cultures of normal and malignant trophoblast cells, pregnant sera, and sera of patients with choriocarcinoma. Endocrinology 113, 1176–1178.
Nilson J. H., Nejedlik M. T., Virgin J. B., Crowder M. E., and Nett T. M. (1983) Expression of α subunit and luteinizing hormone β genes in the ovine anterior pituitary. J. Biol. Chem. 258, 12087–12090.
Gurr J. A. and Kourides I. A. (1984) Ratios of a to TSHβ mRNA in normal and hypothyroid pituitaries and TSH-secreting tumors. Endocrinology 115, 830–832.
Furth J.P., Moy J., Hershman J., and Ueda G. (1973) Thyrotropic tumor syndrome. Arch. Pathol. 96, 217–226.
Chin W. W., Kronenberg H. M., Dee P. C., Maloof F., and Habener J. F. (1981) Nucleotide sequence of the mRNA encoding the pre-α- subunit of mouse thyrotropin. Proc. Natl. Acad. Sci. USA 78, 5329–5333.
Ricciardi R. P., Miller J. S., and Roberts B. E. (1979) Purification and mapping of specific mRNAs by hybridization-selection and cell-free translation. Proc. Natl. Acad. Sci. USA 76, 4927–4931.
Counis R., Ribot G., Corbani M, Poissonnier M., and Jutisz M. (1981) Cell-free translation of the rat pituitary messenger RNA coding for the precursors of α and β subunits of lutropin. FEBS Lett. 123, 151–155.
Hanahan D. and Meselson M. (1980) Plasmid screening at high colony density. Gene 10, 63–67.
Fiddes J. C. and Goodman H. M. (1979) Isolation, cloning and sequence analysis of the cDNA for the α-subunit of human chorionic gonadotropin. Nature 281, 351–355.
Nilson J. H., Thomason A. R., Cserbak M. T., Moncman C. L., and Woychik R. P. (1983) Nucleotide sequence of a cDNA for the common α subunit of the bovine pituitary glycoprotein hormones. J. Biol. Chem. 258, 4679–4682.
Erwin C. R., Croyle M. L., Donelson J. E., and Maurer R. A. (1983) Nucleotide sequence of cloned complementary deoxyribonucleic acid for the α subunit of bovine pituitary glycoprotein hormones. Biochemistry 22, 4856–4860.
Grunstein M. and Hogness D. S. (1975) Colony hybridization: A method for the isolation of cloned DNAs that contain a specific gene. Proc. Natl. Acad. Sci. USA 72, 3961–3965.
Chin W. W., Maizel J. V. Jr, and Habener J. F. (1983) Differences in sizes of human compared to murine alpha subunits of the glycoprotein hormones arises by a four-codon gene deletion or insertion. Endocrinology 112, 482–485.
Fiddes J. C. and Goodman H. M. (1981) The gene encoding the common alpha subunit of the four human glycoprotein hormones. J. Mol. Appl. Genet. 1, 3–18.
Boothby M., Ruddon R. W., Anderson C., McWilliams D., and Boime I. (1981) A single gonadotropin α-subunit gene in normal tissue and tumor-derived cell-lines. J. Biol. Chem. 256, 5121–5127.
Goodwin R. G., Moncman C. L., Rottman F. M., and Nilson J. H. (1983) Characterization and nucleotide sequence of the gene for the common a subunit of the bovine pituitary glycoprotein hormones. Nucleic Acids Res. 11, 6873–6882.
Gilbert W. (1978) Why genes in pieces? Nature 271, 501.
Compton J. G., Schrader W. T., and O’Malley B. YV. (1983) DNA sequence preference of the progesterone receptor. Proc. Natl. Acad. Sci. USA 80, 16–20.
Hoshina M., Boothby M. R., Hussa R. D., Pattillo R. A., Camel H. M., and Boime I. (1984) Segregation patterns of polymorphic restriction sites of the gene encoding the α subunit of human chorionic gonadotropin in trophoblastic disease. Proc. Natl. Acad. Sci. USA 81, 2504–2507.
Ramabhadran T. V., Reitz B. A., and Tiemeier D. C. (1984) Synthesis and glycosylation of the common a subunit of human glycoprotein hormones in mouse cells. Proc. Natl. Acad. Sci. USA 81, 6701–6705.
Fiddes J. C. and Goodman H. M. (1980) The cDNA for the β-subunit of human chorionic gonadotropin suggests evolution by read-through into the 3’-untranslated region. Nature 286, 684–687.
Boorstein W. R., Vamvakopoulos N. C., and Fiddes J. C. (1982) Human chorionic gonadotropin β-subunit is encoded by at least eight genes arranged in tandem and inverted pairs. Nature 300, 419–422.
Talmadge K., Vamvakopoulos N. C., and Fiddes J. C. (1984) Evolution of the genes for the β subunits of human chorionic gonadotropin and luteinizing hormone. Nature 307, 37–40.
Talmadge K., Boorstein W. R., and Fiddes J. C. (1983) The human genome contains seven genes for the beta-subunit of chorionic gonadotropin but only one gene for the beta-subunit of luteinizing hormone. DNA 2, 281–289.
Fiddes J. C. and Talmadge K. (1984) Structure, expression, and evolution of the genes for the human glycoprotein hormones. Recent Prog. Horm. Res. 40, 43–78.
Policastro P., Ovitt C. D., Hoshina M., Fukuoka H., Boothby M. R., and Boime I. (1983) The β subunit of human chorionic gonadotropin is encoded by multiple genes. J. Biol. Chem. 258, 11492–11499.
Keutmann H. T. and Williams R. M. (1977) Human chorionic gonadotropin: Amino acid sequence of the hormone-specific COOH-terminal region. J. Biol. Chem. 252, 5393–5397.
Rigby W. J., Dieckmann M., Rhodes C., and Berg P. (1977) Labeling of deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I. J. Mol. Biol. 113, 237–251.
Chin W. W., Codine J. E.,Klein D. R., Chang A. S., Tan L. K., and Habener J. F. (1983) Nucleotide sequence of the cDNA encoding the precursor of the β subunit of rat lutropin. Proc. Natl. Acad. Sci. USA 80, 4649–4653.
Jameson J. L., Chin W. W., Hollenberg A. N., Chang A. S., and Habener J. F. (1984) The gene encoding the β subunit of rat luteinizing hormone: Analysis of gene structure and evolution of nucleotide sequence. J. Biol. Chem. 259, 15474–15480.
Tepper M. A. and Roberts J. L. (1984) Evidence for only one β-luteinizing hormone and no β-chorionic gonadotropin gene in the rat. Endocrinology 115, 385–391.
Carr F. E. and Chin W. W. (1985) Absence of detectable chorionic gonadotropin mRNAs in rat placenta during gestation. Endocrinology, 116, 1151–1157.
Wurzel J. M., Curatola L. M., Gurr J. A., Goldschmidt A. M., and Kourides I. A. (1983) The luteotropic activity of rat placenta is not due to a chorionic gonadotropin. Endocrinology 83, 1854–1857.
Gurr J. A., Catterall J. F., and Kourides I. A. (1983) Cloning of cDNA encoding the pre-β subunit of mouse thyrotropin. Proc. Natl. Acad. Sci. USA 80, 2122–2126.
Maurer R. A., Croyle M. L., and Donelson J. E. (1984) The sequence of a cloned cDNA for the β subunit of bovine thyrotropin predicts a protein containing both NH.-and COOH-terminal extensions. J. Biol. Chem. 255, 5024–5025.
Chin W. W., Muccini J. A., and Shin L. (1985) Evidence for a single rat thyrotropin-β-subunit gene: Thyroidectomy increases its mRNA. Biochem. Biophy. Res. Commun. 128, 1152–1158.
Croyle M. L. and Maurer R. A. (1984) Thyroid hormone decreases thyrotropin p subunit mRNA levels in rat anterior pituitary. DNA 3, 231–236.
Kourides I. A., Gurr J. A., and Wolf D. (1984) The regulation and organization of thyroid stimulating hormone genes. Recent Prog. Horm. Res. 40, 79–120.
Naylor S. L., Chin W. W., Goodman H. M. Lalley P. A., Grzeschik K. H., and Sakaguchi A. Y. (1983) Chromosomal assignment of genes encoding the a and β subunits of glycoprotein hormones in man and mouse. Sotnatic Cell Genet. 9, 757–770.
JulierC., Weil D., Couillin P., Cote J. C., Nguyen V. C., Foubert C., Boue A., Thirion J. P., Kaplan J. C., and Junien C. (1984) The beta chorionic gonadotropin-beta luteinizing hormone gene cluster maps to human chromosome 19. Hum. Genet. 67, 174–177.
Hardin J. W., Riser M. E., Trent J. M., and Kohler P. O. (1983) The chorionic gonadotropin α subunit gene is on human chromosome 18 in J EG cells. Proc. Natl. Acad. Sci. USA 80, 6282–6285.
Hardin J. W., Riser M., and Kohler P. O. (1984) Chorionic gonadotropin β-subunit gene is on chromosome 10 in J EG cells. Clin. Res. 32, 549A.
Kohler P. O., Riser M., Hardin J., Boothby M., Boime I., Norris J., and Siciliano M. J. (1981) Chorionic gonadotropin synthesis and gene assignment in human: mouse hybrid cells. Adv. Exp. Med. Biol. 138, 405–418.
Kourides I. A., Baker P. E., Gurr J. A., Pravtcheva D. D., and Ruddle F. H. (1984) Assignment of the genes for the α and β subunits of thyrotropin to different mouse chromosomes. Proc. Natl. Acad. Sci. USA 81, 517–519.
Shupnik M. A., Chin W. W., Ross D. S., Downing M. S., Habener J. F., and Ridgway E. C. (1983) Regulation of alpha mRNA levels in the thyrotrope by thyroxine (T4). J. Biol. Chem. 258, 15120–15124.
Chin W. W., Shupnik M. A., Ross D. S., Habencr J. F., and Ridgway E. C. (1985) Regulation of the α and β TSH subunit mRNAs by thyroid hormones. Endocrinology, 116, 873–878.
Gurr J. A. and Kourides I. A. (1983) Regulation of thyrotropin biosynthesis: Discordant effect of thyroid hormone on α and β subunit mRNA levels. J. Biol. Chem. 258, 10208–10211.
Gershengorn M. C., Cohen M., and Hoffstein S. T. (1978) Cellular heterogeneity in primary monolayer cultures of mouse pituitary thyrotropic tumors. Endocrinology 103, 648–651.
Shupnik M. A., Chin W. W., Habener J. F., and Ridgway E. C. (1985) Transcriptional regulation of the thyrotropin subunit genes by thyroid hormone. J. Biol. Chem., 260, 2900–2903.
Brock M. L. and Shapiro D. J. (1983) Estrogen stabilizes vitellogenin mRNA against cytoplasmic degradation. Cell 34, 207–214.
Guyette W. A., Matusik R. J., and Rosen J. M. (1979) Prolactin- mediated transcriptional and post-transcriptional control of casein gene expression. Cell 17, 1013–1023.
McKnight G. S. and Palmiter R. D. (1979) Transcriptional regulation of the ovalbumin and conalbumin genes by steroid hormones in chick oviduct. J. Biol. Chem. 254, 9050–9058*.
Tepper M. A., Dionne F. R., Eberwine J. H., Wilcox J. N., Roberts J. L. (1984) Regulation of beta LH gene expression during the estrus cycle and castration in the rat. 7th International Congress of Endocrinology, Quebec City, Canada. Abstract no. 2293.
Landefeld T. D., Kepa J., and Karsch F. J. (1983) Regulation of α subunit synthesis by gonadal steroid feedback in the sheep anterior pituitary. J. Biol. Chem. 258, 2390–2393.
Landefeld T. and Kepa J. (1984) Regulation of LH beta subunit mRNA in the sheep pituitary gland during different feedback states of estradiol. Biochem. Biophys. Res. Commun. 122, 1307–1313.
Corbani M., Counis R., Starzec A., and Jutisz M. (1984) Effect of gonadectomy on pituitary levels of mRNA encoding gonadotropin subunits and secretion of luteinizing hormone. Mol. Cell. Endocrinol. 35, 83–87.
Counis R., Corbani M., and Jutisz M. (1983) Estradiol regulates mRNAs encoding precursors to rat lutropin (LH) and follitropin (FSH) subunits. Biochem. Biophys. Res. Commun. 114, 65–72.
Chin W. W. (1985) Organization and Expression of Glycoprotein Hormone Genes, in The Pituitary Gland ( Imura H., ed.), Raven, New York.
Gharib S. D., Bowers S. M., Need L. R., and Chin W. W. (1986) Regulation of rat luteinizing hormone (LH) subunit mRNAs by gonadal-steroid hormones. J. Clin. Invest. 77, 582–589.
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1987 The Humana Press Inc.
About this chapter
Cite this chapter
Chin, W.W. (1987). Glycoprotein Hormone Genes. In: Habener, J.F. (eds) Molecular Cloning of Hormone Genes. Molecular Biology and Biophysics. Humana Press. https://doi.org/10.1007/978-1-4612-4824-8_7
Download citation
DOI: https://doi.org/10.1007/978-1-4612-4824-8_7
Publisher Name: Humana Press
Print ISBN: 978-1-4612-9178-7
Online ISBN: 978-1-4612-4824-8
eBook Packages: Springer Book Archive