Skip to main content

Growth Hormone Gene Expression: Hormonal Regulation and Tissue-Specific Expression

  • Chapter
Basic and Clinical Aspects of Growth Hormone

Abstract

Growth hormone (GH) belongs to a family of polypeptide hormones that includes chorionic somatomammotropin (CS, placental lactogen), prolactin (Prl) and proliferin. This hormone family is related by structural homology (1–5), immunoreactivity and partially overlapping biological functions (6). GH and Prl are essential for the normal growth and development of mammals (7,8). GH is required for statural growth and maintenance of nitrogen, mineral, lipid and carbohydrate metabolism (7). Prl is required for the initiation and maintenance of lactation (8). Proliferin may be involved in cellular growth as it occurs in increased concentrations prior to cell division (5,9). The function of CS has been postulated to provide GH-like activities for the developing fetus (10,11); however, it does not appear to have essential functions in man. It appears that a common function of the various members of the growth hormone family may be at the level of control of cellular differentiation and proliferation.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

eBook
USD 16.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 54.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Catt KJ, Moffat B, Niall HD. Human growth hormone and placental lactogen: structural similarity. Science 1967; 157: 321.

    Article  PubMed  CAS  Google Scholar 

  2. Li CH, Dixon JS, Lo TB, Pankov YM, Schmidt KD. Amino acid sequence of ovine lactogenic hormone. Nature 1967; 224: 695.

    Article  Google Scholar 

  3. Sherwood LM. Similarities in the chemical structure of human placental lactogen and pituitary growth hormone. Proc Natl Acad Sci USA 1967; 58: 2307.

    Google Scholar 

  4. Niall HD, Hogan ML, Sayer R, Rosenblum IY, Greenwood FC. Sequences of pituitary and placental lactogenic and growth hormones: evolution from a primordial peptide by gene duplication. Proc Natl Acad Sci USA 1971; 68: 866.

    Article  PubMed  CAS  Google Scholar 

  5. Linzer DIH, Nathans D. Nucleotide sequence of a growth-related mRNA encoding a member of the prolactin-growth hormone family. Proc Natl Acad Sci USA 1984; 81: 4255.

    Article  PubMed  CAS  Google Scholar 

  6. Niall HD, Hogan ML, Tregar GW, Segre GV, Hwang P, Friesen H. The chemistry of growth hormone and the lactogenic hormones. Recent Prog Horm Res 1973; 29: 387.

    PubMed  CAS  Google Scholar 

  7. Martin JB. Neural regulation of growth hormone secretion. N Engl J Med 1973; 288: 1384.

    Article  PubMed  CAS  Google Scholar 

  8. Bern HA, Nicoll CS. The comparative endocrinology of prolactin. Recent Prog Horm Res 1968; 24: 681.

    PubMed  CAS  Google Scholar 

  9. Linzer DIH, Nathans D. Growth-related changes in specific mRNAs of cultured mouse cells. Proc Natl Acad Sci USA 1983; 80: 4271.

    Article  PubMed  CAS  Google Scholar 

  10. Simpson ER, MacDonald PC. Endocrine physiology of the placenta. Annu Rev Physiol 1968; 43: 163.

    Article  Google Scholar 

  11. Grumbach MM, Kaplan SL, Vinik A. HCS physiology: hormonal effects. In: Berson SA, Yalow RS, eds. Peptide hormones. Amsterdam: North Holland Publishing Company, 1973: 797.

    Google Scholar 

  12. Miller WL, Eberhardt NL. Structure and evolution of the growth hormone gene family. Endocr Rev 1983; 4: 97.

    Article  PubMed  CAS  Google Scholar 

  13. Owerbach D, Rutter WJ, Martial JA, Baxter JD, Shows TB. Genes for growth hormone, chorionic somatommamotropin and a growth hormone-like gene are located on chromosome 17 in humans. Science 1980; 209: 289.

    Article  PubMed  CAS  Google Scholar 

  14. George DL, Phillips JA III, Francke V, Seeburg PH. The genes for growth hormone and chorionic somatomammotropin are on the long arm of human chromosome 17 in region q21-qter. Hum Genet 1981; 57: 138.

    Article  PubMed  CAS  Google Scholar 

  15. DeNoto FM, Moore DD, Goodman HM. Human growth hormone DNA sequence and mRNA structure: possible alternative splicing. Nucleic Acids Res 1981; 9: 3719.

    Article  PubMed  CAS  Google Scholar 

  16. Seeburg PH. The human growth hormone gene family: nucleotide sequences show recent divergence and predict a new polypeptide hormone. DNA 1982; 1: 239.

    Article  PubMed  CAS  Google Scholar 

  17. Frankenne F, Rentier-Delrue F, Scippo M-L, Martial J, Hennen G. Expression of the growth hormone variant gene in human placenta. J Clin Endocrinol Metab 1987; 64: 635.

    Article  PubMed  CAS  Google Scholar 

  18. Hirt H, Kimelman J, Birnbaum MJ, et al. The human growth hormone gene locus: structure, evolution, and allelic variations. DNA 1987; 6: 59.

    Article  PubMed  CAS  Google Scholar 

  19. Selby MJ, Barta A, Baxter JD, Bell GI, Eberhardt NL. Analysis of a major human chorionic somatomammotropin gene: evidence for two functional promoter elements. J Biol Chem 1984; 259: 13131.

    PubMed  CAS  Google Scholar 

  20. Barsh GS, Seeburg PH, Gelinas RE. The human growth hormone gene family: structure and evolution of the chromosomal locus. Nucleic Acids Res 1983; 11: 3939.

    Article  PubMed  CAS  Google Scholar 

  21. Duckworth ML, Peden LM, Friesen HG. Isolation of a novel prolactinlike cDNA clone from developing rat placenta. J Biol Chem 1986; 261: 10879.

    PubMed  CAS  Google Scholar 

  22. Duckworth ML, Kirk KL, Friesen HG. Isolation and identification of a cDNA clone of rat placental lactogen II. J Biol Chem 1986; 261: 10871.

    PubMed  CAS  Google Scholar 

  23. Spindler SR, Mellon SH, Baxter JD. Growth hormone gene transcription is regulated by thyroid and glucocorticoid hormones in cultured rat pituitary tumor cells. J Biol Chem 1982; 257: 1 1627.

    Google Scholar 

  24. Evans RM, Birnberg NC, Rosenfeld MG. Glucocorticoid and thyroid hormones transcriptionally regulate growth hormone gene expression. Proc Natl Acad Sci USA 1982; 79: 7659.

    Article  PubMed  CAS  Google Scholar 

  25. Cattini PA, Anderson TR, Baxter JD, Mellon P, Eberhardt NL. The human growth hormone gene is negatively regulated by triiodothyronine when transfected into rat pituitary tumor cells. J Biol Chem 1986; 261: 13367.

    PubMed  CAS  Google Scholar 

  26. Casanova J, Copp RP, Janocko L, Samuels HH. 5′-flanking DNA of the rat growth hormone gene mediates regulated expression by thyroid hormone. J Biol Chem 1985; 260: 1 1744.

    Google Scholar 

  27. Crew MD, Spindler SR. Thyroid hormone regulation of the transfected rat growth hormone promoter. J Biol Chem 1986; 261: 5018.

    PubMed  CAS  Google Scholar 

  28. Larsen RP, Harney JW, Moore DD. Sequences required for cell-type specific thyroid hormone regulation of the rat growth hormone promoter activity. J Biol Chem 1986; 261: 14373.

    PubMed  CAS  Google Scholar 

  29. Wright PA, Crew MD, Spindler SR. Discrete positive and negative thyroid hormone-responsive transcription regulatory elements of the rat growth hormone gene. J Biol Chem 1987; 262: 5659.

    Google Scholar 

  30. Flug F, Copp RP, Casanova J, et al. cis-Acting elements of the rat growth hormone gene which mediate basal and regulated expression by thyroid hormone. J Biol Chem 1987; 262: 6373.

    PubMed  CAS  Google Scholar 

  31. Ivarie RD, Schacter BS, O’Farrell PH. The level of expression of the rat growth hormone gene in liver tumor cells is at least eight orders of magnitude less than in anterior pituitary cells. Mol Cell Biol 1983; 3: 1460.

    PubMed  CAS  Google Scholar 

  32. Karin M, Eberhardt NL, Mellon SH, et al. Expression and hormonal regulation of the rat growth hormone gene in transfected mouse L cells. DNA 1984; 3: 147.

    Article  PubMed  CAS  Google Scholar 

  33. West BL, Catanzaro DF, Mellon SH, Cattini PA, Baxter JD, Reudelhuber TL. Interaction of a tissue-specific factor with an essential rat growth hormone gene promoter element. Mol Cell Biol 1987; 7: 1193.

    PubMed  CAS  Google Scholar 

  34. Catanzaro DL, West BL, Baxter JD, Reudelhuber TL. A pituitary- specific factor interacts with an upstream promoter element in the rat growth hormone gene. Mol Endocrinol 1987; 1: 90.

    Article  PubMed  CAS  Google Scholar 

  35. Lefevre C, Imagawa M, Dana S, Grindlay J, Bodner M, Karin M. Tissue-specific expression of the human growth hormone gene is conferred in part by the binding of a specific trans-acting factor. EMBO J 1987; 66: 971.

    Google Scholar 

  36. Coiro V, Braverman LE, Christiansen D, Fang S-L, Goodman HM. Effect of hypothyroidism and thyroxine replacement on growth hormone in the rat. Endocrinology 1979; 105: 641.

    Article  PubMed  CAS  Google Scholar 

  37. Frantz AG, Rabkin MT. Human growth hormone: clinical measurement, response to hypoglycemia and suppression by glucocorticoids. N Engl J Med 1964; 271: 1375.

    Article  PubMed  CAS  Google Scholar 

  38. Katz HP, Youlton R, Kaplan SL, Grumbach MM. Growth and growth hormone. III. Growth hormone release in children with primary hypothyroidism and thyrotoxicosis. J Clin Endocrinol Metab 1969; 29: 346.

    Google Scholar 

  39. MacGillvray MH, Aceto T Jr, Frohman LA. Plasma growth hormone responses and growth retardation of hypothyroidism. Am J Dis Child 1968; 115: 273.

    Google Scholar 

  40. Adams EF, Brajkovich IE, Mashiter K. Growth hormone and prolactin secretion by dispersed cell cultures of human pituitary adenomas: long term effects of hydrocortisone, estradiol, insulin, 3,5,3′- triiodothyronine and thyroxine. J Clin Endocrinol Metab 1981; 53: 381.

    Article  PubMed  CAS  Google Scholar 

  41. Cattini PA, Peritz LN, Anderson TR, Baxter JD, Eberhardt NL. The 5′-flanking sequences of the human growth hormone gene contain a cell-specific control element. DNA 1986; 5: 503.

    Article  PubMed  CAS  Google Scholar 

  42. Cattini PA, Eberhardt NL. Regulated expression of chimaeric genes containing the 5′-flanking region of human growth hormone-related genes in transiently transfected rat anterior pituitary cells. Nucleic Acids Res 1987; 15: 1297.

    Article  PubMed  CAS  Google Scholar 

  43. Robins DM, Peak I, Seeburg PH, Axel R. Regulated expression of human growth hormone gene in mouse L cells. Cell 1982; 29: 623.

    Article  PubMed  CAS  Google Scholar 

  44. Slater EP, Rabenau O, Karin M, Baxter JD, Beato M. Glucocorticoid receptor binding and activation of a heterologous promoter by dexamethasone by the first intron of the human growth hormone gene. Mol Cell Biol 1985; 5: 2984.

    Google Scholar 

  45. Nelson C, Crenshaw EB III, Franco R. Discrete cis-active genomic sequences dictate the pituitary cell type-specific expression of rat prolactin and growth hormone genes. Nature 1986; 322: 557.

    Article  PubMed  CAS  Google Scholar 

  46. Isaacs RE, Findell PR, Mellon P, Wilson CB, Baxter JD. Hormonal regulation of expression of the endogenous and transfected human growth hormone gene (submitted for publication).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1988 Plenum Press, New York

About this chapter

Cite this chapter

Eberhardt, N.L. et al. (1988). Growth Hormone Gene Expression: Hormonal Regulation and Tissue-Specific Expression. In: Bercu, B.B. (eds) Basic and Clinical Aspects of Growth Hormone. Serono Symposia, USA. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-5505-2_1

Download citation

  • DOI: https://doi.org/10.1007/978-1-4684-5505-2_1

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4684-5507-6

  • Online ISBN: 978-1-4684-5505-2

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics