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Spontaneous 6-thioguanine-resistant lymphocytes in Fanconi anemia patients and their heterozygous parents

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Summary

The incidence of spontaneous 6-thioguanine-resistant (TGr) lymphocytes was studied in the peripheral blood collected from seven Fanconi anemia (FA) patients and five of their heterozygous parents using an autoradiographic or a lymphocyte cloning method. Five of the seven patients showed a significantly elevated incidence of TGr lymphocytes as compared to age- and sex-matched healthy controls. There was, however, no difference between FA heterozygotes and controls. These results suggest some variability among the patients similar to those reported in clinical and cytogenetic investigations. The basis for the increase in TGr cells in the patients is not known, but the inherent genomic instability reflected as increased frequencies of chromosomal aberrations is one possible explanation.

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References

  • Albertini RJ, Allen EF, Quinn AS, Albertini MR (1981) Human somatic cell mutation: In vivo variant lymphocyte frequencies as determined by 6-thioguanine resistance. In: Hook EB, Porter IH (eds) Populations and biological aspects of human mutation. Birth defects Institute symposium XI. Academic Press, New York, pp 235–263

    Google Scholar 

  • Albertini RJ, Castle KL, Borcherding WR (1982) T-cell cloning to detect the mutant 6-thioguanine-resistant lymphocytes present in human peripheral blood. Proc Natl Acad Sci USA 79:6617–6621

    Google Scholar 

  • Auerbach AD, Wolman SR (1978) Carcinogen-induced chromosome breakage in Fanconi's anaemia heterozygous cells. Nature 271:69–71

    Google Scholar 

  • Auerbach AD, Adler B, Chaganti RSK (1981) Prenatal and postnatal diagnosis and carrier detection in Fanconi's anemia by cytogenetic method. Pediatrics 67:128–135

    Google Scholar 

  • Berger R, Bernheim A, le Coniat M, Vecchione D, Schaison G (1980) Sister chromatid exchanges induced by nitrogen mustard in Fanconi's anemia. Application to the detection of heterozygotes and interpretation of the results. Cancer Genet Cytogenet 2:259–267

    Google Scholar 

  • Cohen MM, Simpson SJ, Honig GR, Maurer HS, Nicklas JW, Martin AO (1982) The identification of Fanconi's anemia genotypes by clastogenic stress. Am J Hum Genet 34:794–811

    Google Scholar 

  • Cox R, Masson WK (1976) The isolation and preliminary characterization of 6-thioguanine-resistant mutants of human diploid fibroblasts. Mutat Res 36:93–104

    Google Scholar 

  • Cox R, Masson WK (1978) Do radiation-induced thioguanine-resistant mutants of cultured mammalian cells arise by HGPRT gene mutation or X-chromosomal rearrangement? Nature 276:629–630

    Google Scholar 

  • Dempsey JL, Morley AA, Seshadri RS, Emmerson BT, Gordon R, Bhagat CI (1983) Detection of the carrier state for an X-linked disorder, the Lesch-Nyhan syndrome. Hum Genet 64:288–291

    Google Scholar 

  • deRuijter YCEM, Simons JWIM (1980) Determination of the expression time and the dose-response relationship for mutations at the HGPRT (hypoxanthine-guanine phosphoribosyl transferase) locus induced by X-irradiation in human diploid skin fibroblasts. Mutat Res 69:325–332

    Google Scholar 

  • Duckworth-Rysiecki G, Hulten M, Mann J, Taylor AMR (1984) Clinical and cytogenetic diversity in Fanconi's anaemia. J Med Genet 21:197–203

    Google Scholar 

  • Dutrillaux B, Aurias A, Dutrillaux AM, Buriot D, Prieur M (1982) The cell cycle of lymphocytes in Fanconi's anemia. Hum Genet 62:327–332

    Google Scholar 

  • Evans HJ, Vijayalaxmi (1981) Induction of 8-azaguanine resistance and sister chromatid exchange in human lymphocytes exposed to mitomycin C and X-rays in vitro. Nature 292:601–605

    Google Scholar 

  • Finkelberg R, Buchwald M, Siminovitch L (1977) Decreased mutagenesis in cells from patients with Fanconi's anemia. Am J Hum Genet 29:42A

    Google Scholar 

  • German J (1983a) Patterns of neoplasia associated with the chromosome breakage syndromes. In: German J (ed) Chromosome mutation and neoplasia. Alan R Liss, New York, pp 97–134

    Google Scholar 

  • German J (1983b) Bloom's syndrome. X. The cancer proneness points to chromosome mutation as a crucial event in human neoplasia. In: German J (ed) Chromosome mutation and neoplasia. Alan R Liss, New York, pp 347–357

    Google Scholar 

  • Gupta RS, Goldstein S (1980) Diphtheria toxin resistance in human fibroblast cell strains from normal and cancer-prone individuals. Mutat Res 73:331–338

    Google Scholar 

  • Ling NR, Kay JE (1975) In: Lymphocyte stimulation. North-Holland/Elsevier, Amsterdam, pp 237–252

    Google Scholar 

  • Marx MP, Smith S, Heyns AP, von Tonder IZ (1983) Fanconi's anemia: A cytogenetic study on lymphocytes and bone marrow cultures utilizing 1,2;3,4 diepoxybutane. Cancer Genet Cytogenet 9:51–60

    Google Scholar 

  • Miura K, Morimoto K, Koizumi A (1983) Proliferative kinetics and mitomycin C-induced chromosome damage in Fanconi's anemia lymphocytes. Hum Genet 63:19–23

    Google Scholar 

  • Morley AA, Trainor KJ, Seshadri R, Ryall RG (1983) Measurement of in vivo mutations in human lymphocytes. Nature 294:697–699

    Google Scholar 

  • Natarajan AT, Meijers M, van Rijn JLS (1982) Individual variability of human cells in induction of chromosomal alterations by mutagens. In: Sorsa M, Vainio H (eds) Mutagens in our environment. Proc XII annual meeting of EEMS, Finland. Alan R Liss Inc, New York, pp 75–78

    Google Scholar 

  • Paul WE, Sredni B, Schwartz RH (1982) Long-term growth and cloning of non-transformed lymphocytes Nature 294:697–699

    Google Scholar 

  • Ray JH, German J (1981) The chromosome changes in Bloom's syndrome, ataxia telangiectasia and Fanconi's anemia. In: Arrighi E, Rao P, Stubblefield E (eds) Genes, chromosomes and neoplasia. Raven Press, New York, pp 351–378

    Google Scholar 

  • Sanderson BJS, Dempsey JL, Morley AA (1984) Mutations in human lymphocytes: Effect of X- and UV-irradiation. Mutat Res 140:223–227

    Google Scholar 

  • Schrocder TM (1972) Genetische Faktoren der Krebsentstehung. Fortschr Med 90:603–608

    Google Scholar 

  • Schrocder TM (1982) Genetically determined chromosome instability syndromes. Cytogenet Cell Genet 33:119–132

    Google Scholar 

  • Schroeder TM, German J (1974) Bloom's syndrome and Fanconi's anemia: Demonstration of two distinctive patterns of chromosome disruption and rearrangement. Humangenetik 25:299–306

    Google Scholar 

  • Strauss GH, Albertini RJ (1979) Enumeration of 6-thioguanine-resistant peripheral blood lymphocytes in man as a potential test for somatic cell mutations arising in vivo. Mutat Res 61:353–379

    Google Scholar 

  • Swift MR (1971) Fanconi's anemia in the genetics of neoplasia. Nature 230:370–373

    Google Scholar 

  • Swift MR, Caldwell RJ, Chase C (1980) Reassessment of cancer predisposition of Fanconi's anemia heterozygotes. JNCI 65:863–867

    Google Scholar 

  • Todaro GJ, Green H, Swift MR (1966) Susceptibility of human diploid fibroblast strains to transformation by SV40 virus. Science 153:1252–1254

    Google Scholar 

  • Vijayalaxmi, Evans HJ (1984a) Measurement of spontaneous and X-irradiation-induced 6-thioguanine-resistant human blood lymphocytes using a T-cell cloning technique. Mutat Res 125:87–94

    Google Scholar 

  • Vijayalaxmi, Evans HJ (1984b) Induction of 6-thioguanine-resistant mutants and SCEs by three chemical mutagens (EMS, ENU and MMC) in cultured human blood lymphocytes. Mutat Res 129:283–289

    Google Scholar 

  • Vijayalaxmi, Evans HJ, Ray JH, German J (1983) Bloom's syndrome: Evidence for an increased mutation frequency in vivo. Science 221:851–853

    Google Scholar 

  • von Koskull H, Aula P (1977) Distribution of chromosome breaks in measles, Fanconi's anemia and controls. Hereditas 87:1–10

    Google Scholar 

  • Warren ST, Schultz RA, Chang CC, Wade MH, Trosko JE (1981) Elevated spontaneous mutation rate in Bloom syndrome fibroblasts. Proc Natl Acad Sci USA 78:3133–3137

    Google Scholar 

  • Wunder E, Fleischer-Reischmann B (1983) Response of lymphocytes from Fanconi's anemia patients and their heterozygous relatives to 8-methoxy-psoralene in a cloning survival test system. Hum Genet 64:167–173

    Google Scholar 

  • Zakrzewski S, Koch M, Sperling K (1983) Complementation studies between Fanconi's anemia cells with different DNA repair characteristics. Hum Genet 64:55–57

    Google Scholar 

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Vijavalaxmi, Wunder, E. & Schroeder, T.M. Spontaneous 6-thioguanine-resistant lymphocytes in Fanconi anemia patients and their heterozygous parents. Hum Genet 70, 264–270 (1985). https://doi.org/10.1007/BF00273454

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