The cell cycle of lymphocytes in Fanconi anemia (original) (raw)
Summary
BrdU-incorporation techniques were used to study the cell cycle in 18 cases of Fanconi's anemia (FA).
By comparison with controls, a significant slowing of the cell cycle of lymphocytes in vitro was observed in all FA patients, and possibly in FA heterozygotes, although to a lesser degree. It is probable that the demonstration of the slowing is dependent on the culture conditions. No slowing was observed in other patients affected by at least one of the symptoms of FA. The slow cell cycle of FA cells is mostly due to a very long G2-phase. A relationship between slow cell cycle and chromatid anomalies exists, the slower cells being significantly more frequently carriers of radial figures than the faster cells, in the same patient.
Access this article
Subscribe and save
- Starting from 10 chapters or articles per month
- Access and download chapters and articles from more than 300k books and 2,500 journals
- Cancel anytime View plans
Buy Now
Price excludes VAT (USA)
Tax calculation will be finalised during checkout.
Instant access to the full article PDF.
Similar content being viewed by others
References
- Addison M, Rice MS (1965) The association of dyskeratosis congenita and Fanconi's anemia. Med J Aust 1:797–799
Google Scholar - Auerbach AD, Wolman SR (1976) Susceptibility of Fanconi's anemia fibroblasts to chromosome damage by carcinogens. Nature 261: 494–496
Google Scholar - Auerbach AD, Wolman SR (1978) Carcinogen-induced chromosome breakage in Fanconi's anemia heterozygous cells. Nature 271:69–71
Google Scholar - Berger R, Bernheim A, Le Coniat M, Vecchione D, Schaison G (1980) Effet du chlorhydrate de chlorméthine sur les chromosomes dans l'anémie de Fanconi: application au diagnostic et à la détection des hétérozygotes. CR Acad Sci (Paris) 290:457–459
Google Scholar - Dutrillaux B (1977) New chromosome techniques. In: Yunis JJ (ed) Molecular structure of human chromosomes. Academic Press, New York San Francisco London, pp 233–265
Google Scholar - Dutrillaux B, Laurent C, Couturier J, Lejeune J (1973) Coloration par l'acridine orange des chromosomes préalablement traités par le 5-bromodéoxyuridine. CR Acad Sci (Paris) 276:3179–3181
Google Scholar - Dutrillaux B, Fosse AM, Prieur M, Lejeune J (1974) Analyse des échanges de chromatides dans les cellules somatiques humaines. Traitement au BUDR (5-bromodéoxyuridine) et fluorescence bicolore par l'acridine orange. Chromosoma 48:327–340
Google Scholar - Dutrillaux B, Fosse AM (1976) Utilisation du BrdU dans l'étude du cycle cellulaire des sujets normaux et anormaux. Ann Génét 19:95–102
Google Scholar - Hirsch-Kauffmann M, Schweiger M, Wagner EF, Sperling K (1978) Deficiency of DNA ligase activity in Fanconi's anemia. Hum Genet 45:25–32
Google Scholar - Latt SA, Stetten G, Juergens LA, Buchanan GR, Gerald PS (1975) Induction by alkylating agents of sister chromatid exchanges and chromatid breaks in Fanconi's anemia. Proc Nat Acad Sci USA 72:4066–4070
Google Scholar - Mutchinick O, Ruz L, Gonsebatt ME, Mauleon P, Lisker R, Garcia G (1981) Frequency and types of induced and spontaneous chromosome aberrations in relation to cell kinetics. Hum Genet 59:137–140
Google Scholar - Nordenson I (1977) Effet of superoxide dismutase and catalase on spontaneously occurring chromosome breaks in patients with Fanconi's anemia. Hereditas 86:147–150
Google Scholar - Perry P, Wolff S (1974) New Giemsa method for the differential staining of sister chromatids. Nature 251:156–158
Google Scholar - Poon PK, O'Brien RL, Parker JW (1974) Defective DNA repair in Fanconi's anemia. Nature 250:223–225
Google Scholar - Sasaki MS (1975) Is Fanconi's anemia defective in a process essential to the repair of DNA cross links? Nature 257:501–503
Google Scholar - Sasaki MS, Tonomura A (1973) A high susceptibility of Fanconi's anemia to chromosome breakage by DNA cross-linking agents. Cancer Res 33:1829–1836
Google Scholar - Schroeder TM, Auschütz F, Knopp A (1964) Spontane Chromosomen-aberrationen bei familiärer Panmyelopathie. Hum Genet 1:194–196
Google Scholar - Schuler D, Kiss A, Fabian F (1969) Chromsome peculiarities and in vitro examinations in Fanconi's anemia. Hum Genet 7:314–322
Google Scholar - Schuler D, Dobos M, Fekete G (1979) Chromosome mutations and chromosome instability in children treated with different regimens of immunosuppressive drugs. Hum Hered 29:100–105
Google Scholar
Author information
Authors and Affiliations
- Institut de Progenèse, 15, rue de l'Ecole de Médecine, F-75270, Paris Cedex 06, France
B. Dutrillaux, A. Aurias, Anne-Marie Dutrillaux & Marguerite Prieur - Unité d'Immuno-Hématologie, Hôpital des Enfants-Malades, 149, rue de Sèvres, F-75015, Paris, France
D. Buriot
Authors
- B. Dutrillaux
- A. Aurias
- Anne-Marie Dutrillaux
- D. Buriot
- Marguerite Prieur
Rights and permissions
About this article
Cite this article
Dutrillaux, B., Aurias, A., Dutrillaux, AM. et al. The cell cycle of lymphocytes in Fanconi anemia.Hum Genet 62, 327–332 (1982). https://doi.org/10.1007/BF00304549
- Received: 27 September 1982
- Issue date: December 1982
- DOI: https://doi.org/10.1007/BF00304549