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Journal of Cancer Research and Clinical Oncology logoLink to Journal of Cancer Research and Clinical Oncology
. 1996 Aug;122(8):453–457. doi: 10.1007/BF01187156

Distribution of Gs-α activating mutations in human thyroid tumors measured by subcloning

Victor N Gorelov 1,, Marianna Gyenes 1, Frank Neser 1, Hans-Dieter Röher 1, Peter E Goretzki 1
PMCID: PMC12200093  PMID: 8698744

Abstract

In the search for the prevalence and distribution pattern of Gs-α gene mutations in differentiated thyroid tumors we examined 66 tumor tissue samples for the presence of mutations at “hot-spot” codons 201 and 227 using methods based on the polymerase chain reaction, subcloning and sequencing. the prevailing type of singlebase substitution at codon 201 (71.4%) corresponded to the replacement of the wild-type sequence CGT (Arg) with TGT (Cys). The fragments of the Gs-α gene, including codon 201 or 227 from five follicular carcinomas and one follicular adenoma, were subcloned inEscherichia coli and it was found that the proportion of alleles with mutated codon 201 varied from 3.2% to 43%. Sequencing of the corresponding region has confirmed preliminary data indicating that the single-base changes CGT (Arg) to TGT (Cys) or CGT to CAT (His) occurred. There was only a weak correlation between the prevalence of cells bearing a mutation in the Gs-α gene and the level of Gs-α protein expression in the corresponding thyroid tumors.

Key words: Gs-α gene, Mutations, Subcloning, Sequencing, Thyroid tumors

Abbreviations

RFLP

restriction-fragment-length polymorphism

MSOH

mutation-specific oligonucleotide hybridization

PCR

polymerase chain reaction

Footnotes

This work was supported by a grant from Deutsche Forschungs-gemeinschaft (Go 356/3-1)

References

  1. Bos JL (1989)ras oncogenes in human cancer: a review. Cancer Res 49:4682–4689 [PubMed] [Google Scholar]
  2. Gorelov VN, Röher H-D, Goretzki PE (1994) A method to increase the sensitivity of mutation specific oligonucleotide hybridization using asymmetric polymerase chain reaction (PCR). Biochem Biophys Res Commun 200:365–369 [DOI] [PubMed] [Google Scholar]
  3. Gorelov VN, Dumon K, Barteneva NS, Palm D, Röher H-D, Goretzki PE (1995) Overexpression of Gs-α subunit in thyroid tumors bearing a mutated Gs-α gene. J Cancer Res Clin Oncol 121:219–224 [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Goretzki PE, Lyons J, Stacy-Phipps S, Rosenau W, Demeure M, Clark OH, McCormic Röher H-D, Bourne HR (1992) Mutational activity of RAS and GSP oncogenes in differentiated thyroid cancer and their applications. World J Surg 16:576–581 [DOI] [PubMed] [Google Scholar]
  5. Landis CA, Masters SB, Spada A, Pace AM, Bourne HR, Vallar L (1989) GTPase inhibiting mutations activate the α chain of Gs and stimulate adenylyl cyclase in human pituitary tumors. Nature 340:692–696 [DOI] [PubMed] [Google Scholar]
  6. Landis CA, Harsh G, Lyons J, Davis RL, McCormic F, Bourne HR (1990) Clinical characteristics of acromegalic patients whose pituatry tumors contain mutant Gs protein. J Endocrinol Metab 71:1416–1420 [DOI] [PubMed] [Google Scholar]
  7. Levi S, Urbano-Ispizua A, Gill R, Thomas DM, Gilbertson J, Foster C, Marshall CJ (1991) Multiple K-ras codon 12 mutations in cholangiocarcinomas demonstrated with a sensitive polymerase chain reaction technique. Cancer Res 51:3497–3502 [PubMed] [Google Scholar]
  8. Lyons J, Landis CA, Harsh G, Vallar L, Grünewald K, Feichtinger H, Duh Q-Y, Clark OH, Kawasaki E, Bourne HR, McCormic F (1990) Two G protein oncogenes in human endocrine tumors. Science 249:665–659 [DOI] [PubMed] [Google Scholar]
  9. Matsuo K, Friedman E, Gejman PV, Fagin JA (1993) The thyrotropin receptor (TSH-R) is not an oncogene for thyroid tumors: structural studies of the TSH-R and the α-subunit of Gs in human thyroid neoplasms. J Clin Endocrinol Metab 76:1448–1451 [DOI] [PubMed] [Google Scholar]
  10. Miller RT, Masters SB, Sullivan KA, Biederman B, Bourne HR (1988) A mutation that prevents GTP-dependent activation of the α chain of Gs. Nature 334:712–715 [DOI] [PubMed] [Google Scholar]
  11. Müller A, Gorelov V, Möllner S, Röher H-D, Goretzki PE (1994) Importance of adenylate cyclase and G-protein mutations in prognosis of differentiated thyroid tumors (in German) In: Trede M, Siewert JR, Hartel W (eds) Chirurgishes Forum 1994 für experimentelle und klinische Forchung. Springer, Berlin Heidelberg New York, pp 349–353 [Google Scholar]
  12. Sanger F, Nickeln S, Coulson AR (1977) DNA sequencing with chainterminating inhibitors. Proc Natl Acad Sci USA 74:5463–5467 [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Schwindinger WF, Francomano CA, Levin MA (1992) Identification of a mutation in the gene encoding the α subunit of the stimulatory G protein of adenylyl cyclase in McCune-Albricht syndrome. Proc Natl Acad Sci USA 89:5152–5156 [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Siperstein AE, Miller RA, Landis C, Bourne H, Clark OH (1991) Increased stimulatory G protein in neoplastic human thyroid tissues. Surgery 110:949–955 [PubMed] [Google Scholar]
  15. Spada A, Arosio M, Bochiccio D, Bazzoni N, Vallar L, Bassetti M, Faglia G (1990) Clinical, biochemical, and morphological correlates in patients bearing growth hormone-secreting pituitary tumors with or without constitutively active adenylyl cyclase. J Clin Endocrinol Metab 71: 1421–1426 [DOI] [PubMed] [Google Scholar]
  16. Suarez HG, du Villard JA, Caillou B, Schlumberger M, Permentier C, Monier R (1991) GSP mutations in human thyroid tumors. Oncogene 6:677–679 [PubMed] [Google Scholar]

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