Summary
The location and frequency of folate-sensitive common fragile sites (CFS) were studied in three populations: (1) 111 mentally retarded children of school age, (2) 240 mentally subnormal children attending special schools, and (3) 85 healthy children attending normal schools. Common fragile sites were found at 54 chromosomal bands including also the band Xq27, where gaps and breaks were detected in 4% of the children. The most frequent CFS were FRA3B (at 3p14.2), FRA6E (at 6q26), and FRA16D (at 16q23) seen in 73%, 65%, and 58% of the individuals totally studied. The frequencies of CFS-positive individuals did not differ among the populations. The variation found in the distribution of CFS among the populations was primarily assumed to be due to sampling differences and study method. The rate of expression of the most frequent CFS varied significantly among the individuals, seeming to suggest that polymorphism exists at those CFS.
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References
Aula P, Koskull H von (1976) Distribution of spontaneous chromosome breaks in human chromosomes. Hum Genet 32:143–148
Ayme S, Mattei JF, Mattei MG, Aurran Y, Giraud F (1976) Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects. Hum Genet 31:161–175
Barbi G, Steinbach P, Vogel W (1984) Nonrandom distribution of methotrexate-induced aberrations on human chromosomes. Detection of further folic acid sensitive fragile sites. Hum Genet 68: 290–294
Berger R, Bloomfield CD, Sutherland GR (1985) Report of the committee on chromosome rearrangements in neoplasia and on fragile sites. (8th International Workshop on Human Gene Mapping) Cytogenet Cell Genet 40:490–535
Braekeleer M de, Smith B, Lin CC (1985) Fragile sites and structural rearrangements in cancer. Hum Genet 69:112–116
Craig-Holmes AP, Strong LC, Goodacre A, Pathak S (1987) Variation in the expression of aphidicolin-induced fragile sites in human lymphocyte cultures. Hum Genet 76:134–137
Davis JR, Hagaman RM (1987) Fragile sites are unrelated to reciprocal translocation breakpoints. Clin Genet 31:308–310
Djalali M, Barbi G, Steinbach P (1985) Folic acid sensitive fragile sites are not limited to the human karyotype. Demonstration of nonrandom gaps and breaks in the Persian vole Ellobius lutescens Th. inducible by methotrexate, fluorodeoxyuridine, and aphidicolin. Hum Genet 70:183–185
Glover TW, Stein CK (1987a) Induction of sister chromatid exchanges at common fragile sites. Am J Hum Genet 41:882–890
Glover TW, Stein CK (1987b) Site-specific chromosomal deletions and rearrangements at fragile sites in somatic cell hybrids. 3rd International Workshop on the Fragile X and X-Linked Mental Retardation, Troina 1987 (abstr)
Glover TW, Berger C, Coyle J, Echo B (1984) DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes. Hum Genet 67:136–142
Hecht F (1988) Fragile sites up date. Cancer Genet Cytogenet 31: 125–128
Hecht F, Hecht BK (1984a) Fragile sites and chromosome breakpoints in constitutional rearrangements. I. Amniocentesis. Clin Genet 26:169–173
Hecht F, Hecht BK (1984b) Fragile sites and chromosome breakpoints in constitutional rearrangements. II. Spontaneous abortions, stillbirths and newborns. Clin Genet 26:174–177
Hecht F, Sutherland GR (1984) Fragile sites and cancer breakpoints. Cancer Genet Cytogenet 12:179–181
ISCN (1985) An international system for human cytogenetic nomenclature. In: Harnden DG, Klinger HP (eds) Published in collaboration with Cytogenet Cell Genet. Karger, Basel
Kääriäinen R, Piepponen P, Vaskilampi T (1985) A multi-disciplinary case-control study of mental retardation in children of four birth cohorts. (Community Health, original reports 1, 1985) University of Kuopio, Kuopio
Kähkönen M, Leisti J, Thoden CJ, Autio S (1986) Frequency of rare fragile sites among mentally subnormal school children. Clin Genet 30:234–238
Kähkönen M, Alitalo T, Airaksinen E, Matilainen R, Launiala K, Autio S, Leisti J (1987) Prevalence of the fragile X syndrome in four birth cohorts of children of school age. Hum Genet 77:85–87
Le Beau MM (1986) Chromosomal fragile sites and cancer-specific rearrangements. Blood 67:849–858
Ledbetter SA, Ledbetter DH (1987) A common fragile site at FRAXA (Xq27.3): evidence from aphidicolin induction in normal males. (9th International Workshop on Human Gene Mapping) Cytogenet Cell Genet 46:645
Miró R, Clemente IC, Fuster C, Egozcue J (1987) Fragile sites, chromosome evolution, and human neoplasia. Hum Genet 75:345–349
Opitz J, Sutherland GR (1984) Conference report. International Workshop on the Fragile X and X-Linked Mental Retardation. Am J Med Genet 17:5–94
Smeets DFCM, Scheres JMJC, Hustinx TWJ (1986) The most common fragile site in man is 3p14. Hum Genet 72:215–220
Sutherland GR, Hecht F (1985) Fragile sites on human chromosomes. (Oxford monographs on medical genetics, no 13) Oxford University Press, Oxford
Sutherland GR, Simmers RN (1988) No statistical association between common fragile sites and nonrandom chromosome breakpoints in cancer cells. Cancer Genet Cytogenet 31:9–15
Sutherland GR, Parslow MI, Baker E (1985) New classes of common fragile sites induced by 5-azacytidine and bromodeoxyuridine. Hum Genet 69:233–237
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Kähkönen, M. Population cytogenetics of folate-sensitive fragile sites. Hum Genet 80, 344–348 (1988). https://doi.org/10.1007/BF00273649
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DOI: https://doi.org/10.1007/BF00273649