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Volumn 14, Issue 4, 1996, Pages 400-405

Susceptible chiasmate configurations of chromosome 21 predispose to non- disjunction in both maternal meiosis I and meiosis II

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHROMOSOME CHIASM; CONTROLLED STUDY; FEMALE; GENETIC RECOMBINATION; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; MATERNAL AGE; MEIOSIS; NEWBORN; NONDISJUNCTION; PRIORITY JOURNAL; TRISOMY 21;

EID: 10544226872     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng1296-400     Document Type: Article
Times cited : (320)

References (37)
  • 1
    • 0026000975 scopus 로고
    • Trisomy 21: Association between reduced recombination and nondisjunction
    • Sherman, S.L. et al. Trisomy 21: Association between reduced recombination and nondisjunction. Am.J.Hum.Genet. 49, 608-620 (1991).
    • (1991) Am.J.Hum.Genet. , vol.49 , pp. 608-620
    • Sherman, S.L.1
  • 2
    • 0027980592 scopus 로고
    • Non-disjunction of chromosome 21 in maternal meiosis I: Evidence for a maternal age-dependent mechanism involving reduced recombination
    • Sherman, S.L. et al. Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination. Hum. Mol. Genet. 3, 1529-1535 (1994).
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1529-1535
    • Sherman, S.L.1
  • 3
    • 0030058258 scopus 로고    scopus 로고
    • Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of the chromosomal error: A population-based study
    • Yoon, P.W. et al. Advanced maternal age and the risk of Down syndrome characterized by the meiotic stage of the chromosomal error: a population-based study. Am. J. Hum. Genet. 58, 628-633 (1996).
    • (1996) Am. J. Hum. Genet. , vol.58 , pp. 628-633
    • Yoon, P.W.1
  • 4
    • 0023236677 scopus 로고
    • Evidence for reduced recombination on the nondisjoined chromsome 21 in Down syndrome
    • Warren, A.C. et al. Evidence for reduced recombination on the nondisjoined chromsome 21 in Down syndrome. Science 237, 652-654 (1987).
    • (1987) Science , vol.237 , pp. 652-654
    • Warren, A.C.1
  • 5
    • 0026536404 scopus 로고
    • The meiotic stage of nondisjunction in trisomy 21: Determination by using DNA polymorphisms
    • Antonarakis, S.E. et al. The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms. Am J. Hum. Genet. 50, 544-550 (1992).
    • (1992) Am J. Hum. Genet. , vol.50 , pp. 544-550
    • Antonarakis, S.E.1
  • 6
    • 0027447719 scopus 로고
    • Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age
    • Antonarakis, S.E., Avramopoulos, D., Blouin, J., Talbot, C.C. & Schinzel, A.A. Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age. Nature Genet. 3, 146-150 (1993).
    • (1993) Nature Genet. , vol.3 , pp. 146-150
    • Antonarakis, S.E.1    Avramopoulos, D.2    Blouin, J.3    Talbot, C.C.4    Schinzel, A.A.5
  • 7
    • 0025907673 scopus 로고
    • Parental origin of the extra chromosome in trisomy 21 as indicated by analysis of DNA polymorphisms
    • Antonarakis, S.E. & Down Syndrome Collaborative Group. Parental origin of the extra chromosome in trisomy 21 as indicated by analysis of DNA polymorphisms. New Engl. J. Med. 324, 872-876 (1991).
    • (1991) New Engl. J. Med. , vol.324 , pp. 872-876
    • Antonarakis, S.E.1
  • 8
    • 0028858439 scopus 로고
    • Epidemiology study of Down's syndrome in Denmark, including family studies of chromosomes and DNA markers
    • Mikkeisen, M. et al. Epidemiology study of Down's syndrome in Denmark, including family studies of chromosomes and DNA markers. Dev. Brain Dystunct. 8, 4-12 (1995).
    • (1995) Dev. Brain Dystunct. , vol.8 , pp. 4-12
    • Mikkeisen, M.1
  • 10
    • 0019777124 scopus 로고
    • Recombinationless meiosis in Saccharomyces cerevisiae
    • Malone, R.E. & Esposito, R.E. Recombinationless meiosis in Saccharomyces cerevisiae. Mol. Cell. Biol. 1, 891-901 (1981).
    • (1981) Mol. Cell. Biol. , vol.1 , pp. 891-901
    • Malone, R.E.1    Esposito, R.E.2
  • 12
    • 0027502061 scopus 로고
    • ZIP1 is a synaptonemal complex protein required for meiotic chromosomal synapsis
    • Sym, M., Engebrecht, J. & Roeder, G. ZIP1 is a synaptonemal complex protein required for meiotic chromosomal synapsis. Cell 72, 365-378 (1993).
    • (1993) Cell , vol.72 , pp. 365-378
    • Sym, M.1    Engebrecht, J.2    Roeder, G.3
  • 13
    • 0027142426 scopus 로고
    • Meiotic segregation in Drosophila Melanogaster females: Molecules, mechanisms and myths
    • Hawley, R.S., McKim, K.S. & Arbel, T. Meiotic segregation in Drosophila Melanogaster females: molecules, mechanisms and myths. Annu. Rev. Genet. 27, 281-317 (1993).
    • (1993) Annu. Rev. Genet. , vol.27 , pp. 281-317
    • Hawley, R.S.1    McKim, K.S.2    Arbel, T.3
  • 14
    • 0028133503 scopus 로고
    • Separation anxiety: The biology of non-disjunction in flies and people
    • Hawley, R.S., Frazier, J. & Rasooly, R. Separation anxiety: the biology of non-disjunction in flies and people. Hum. Mol. Genet. 3, 1521-1528 (1994).
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1521-1528
    • Hawley, R.S.1    Frazier, J.2    Rasooly, R.3
  • 15
    • 0026334334 scopus 로고
    • XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region
    • Hassold, T.J., Sherman, S.L., Pettay, D., Page, D.C. & Jacobs, P.A. XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region. Am. J. Hum. Genet. 49, 253-260 (1991).
    • (1991) Am. J. Hum. Genet. , vol.49 , pp. 253-260
    • Hassold, T.J.1    Sherman, S.L.2    Pettay, D.3    Page, D.C.4    Jacobs, P.A.5
  • 16
    • 0028030585 scopus 로고
    • The origin of 47,XXY and 47,XXX aneuploidy: Heterogeneous mechanisms and role of aberrant recombination
    • MacDonald, M. et al. The origin of 47,XXY and 47,XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombination. Hum. Mol. Genet. 3, 1365-1371 (1994).
    • (1994) Hum. Mol. Genet. , vol.3 , pp. 1365-1371
    • MacDonald, M.1
  • 17
    • 0027430806 scopus 로고
    • Nondisjunction of choromsome 15: Origin and recombination
    • Robinson, W.P et al. Nondisjunction of choromsome 15: origin and recombination. Am. J. Hum. Genet. 53, 740-751 (1993).
    • (1993) Am. J. Hum. Genet. , vol.53 , pp. 740-751
    • Robinson, W.P.1
  • 18
    • 0008569611 scopus 로고
    • Perturbed recombination of chromosome 15 in Prader-Willi patients with maternal disomy
    • Mascari, M. J. et al. Perturbed recombination of chromosome 15 in Prader-Willi patients with maternal disomy. Am. J. Hum. Genet. 53, A260 (1993).
    • (1993) Am. J. Hum. Genet. , vol.53
    • Mascari, M.J.1
  • 19
    • 0029118422 scopus 로고
    • Recombination and maternal age-dependent non-disjunction: Molecular studies of trisomy 16
    • Hassold, T., Merrill, M., Adkins, K., Freeman, S. & Sherman, S. Recombination and maternal age-dependent non-disjunction: molecular studies of trisomy 16. Am. J. Hum. Genet. 57, 867-874 (1995).
    • (1995) Am. J. Hum. Genet. , vol.57 , pp. 867-874
    • Hassold, T.1    Merrill, M.2    Adkins, K.3    Freeman, S.4    Sherman, S.5
  • 20
    • 0028907505 scopus 로고
    • Trisomy 18: Studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction
    • Fisher, J.M., Harvey, J.F., Morton, N.E. & Jacobs, P.A. Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction. Am. J. Hum. Genet. 56, 669-675 (1995).
    • (1995) Am. J. Hum. Genet. , vol.56 , pp. 669-675
    • Fisher, J.M.1    Harvey, J.F.2    Morton, N.E.3    Jacobs, P.A.4
  • 21
    • 0026676193 scopus 로고
    • Nondisjunction of chromosome 21: Comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin
    • Lorber, B.J., Grantham, M., Peters, J., Willard, H.F. & Hassold, T.J. Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin. Am. J. Hum. Genet. 51, 1265-1276 (1992).
    • (1992) Am. J. Hum. Genet. , vol.51 , pp. 1265-1276
    • Lorber, B.J.1    Grantham, M.2    Peters, J.3    Willard, H.F.4    Hassold, T.J.5
  • 22
    • 0026785123 scopus 로고
    • Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome
    • Petersen, M.B. et al. Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome. Am. J. Hum. Genet. 51, 516-525 (1992).
    • (1992) Am. J. Hum. Genet. , vol.51 , pp. 516-525
    • Petersen, M.B.1
  • 23
    • 0001927329 scopus 로고
    • Nondisjunction as proof of the chromosome theory of heredity
    • Bridges, C.B. Nondisjunction as proof of the chromosome theory of heredity. Genetics 1, 1-52 (1916).
    • (1916) Genetics , vol.1 , pp. 1-52
    • Bridges, C.B.1
  • 24
    • 0025034508 scopus 로고
    • Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy
    • Hassold, T., Pettay, E., May, K. & Robinson, A. Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy. Hum. Genet. 85, 648-650 (1990).
    • (1990) Hum. Genet. , vol.85 , pp. 648-650
    • Hassold, T.1    Pettay, E.2    May, K.3    Robinson, A.4
  • 25
    • 0028601416 scopus 로고
    • Sister-chromatid cohesion in mitosis and meiosis
    • Miyazaki, W.Y. & Orr-Weaver, T.L. Sister-chromatid cohesion in mitosis and meiosis. Annu. Rev. Genet. 28, 167-187 (1994).
    • (1994) Annu. Rev. Genet. , vol.28 , pp. 167-187
    • Miyazaki, W.Y.1    Orr-Weaver, T.L.2
  • 26
    • 0029020649 scopus 로고
    • Etiology of nondisjunction in humans
    • Abruzzo, M. & Hassold, T.J. Etiology of nondisjunction in humans. Envir. Mol. Mut. 25, 38-47 (1995).
    • (1995) Envir. Mol. Mut. , vol.25 , pp. 38-47
    • Abruzzo, M.1    Hassold, T.J.2
  • 27
    • 0014404553 scopus 로고
    • Chiasma frequency and maternal age in mammals
    • Henderson, S.A. & Edwards, R.G. Chiasma frequency and maternal age in mammals. Nature 217, 22-28 (1968).
    • (1968) Nature , vol.217 , pp. 22-28
    • Henderson, S.A.1    Edwards, R.G.2
  • 28
    • 0022395534 scopus 로고
    • Determination of the parental origin of sex-chromosome monosomy using restriction fragment length polymorphisms
    • Hassold, T.E., Kumlin, E., Takaesu, N. & Leppert, M. Determination of the parental origin of sex-chromosome monosomy using restriction fragment length polymorphisms. Am. J. Hum. Genet. 37, 965-972 (1985).
    • (1985) Am. J. Hum. Genet. , vol.37 , pp. 965-972
    • Hassold, T.E.1    Kumlin, E.2    Takaesu, N.3    Leppert, M.4
  • 29
    • 0027506362 scopus 로고
    • A contiguous physical map of the pericentromeric region of chromosome 21q between D2/Z1 and D21S13E
    • Van Hul, W. et al. A contiguous physical map of the pericentromeric region of chromosome 21q between D2/Z1 and D21S13E. Genomics 15, 626-630 (1993).
    • (1993) Genomics , vol.15 , pp. 626-630
    • Van Hul, W.1
  • 30
    • 0026032076 scopus 로고
    • Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to both
    • Jabs, E.W. et al. Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to both. Genomics 9, 141-146 (1991).
    • (1991) Genomics , vol.9 , pp. 141-146
    • Jabs, E.W.1
  • 31
    • 0023410736 scopus 로고
    • Methods for studying recombination on chromosomes that undergo nondisjunction
    • Chakravarti, A. & Slaugenhaupt, S.A. Methods for studying recombination on chromosomes that undergo nondisjunction. Genomics 1, 35-42 (1987).
    • (1987) Genomics , vol.1 , pp. 35-42
    • Chakravarti, A.1    Slaugenhaupt, S.A.2
  • 32
    • 0025020073 scopus 로고
    • A centromere map of the X chromosome from trisomies of maternal origin
    • Morton, N.E. et al. A centromere map of the X chromosome from trisomies of maternal origin. Ann. Hum. Genet. 54, 39-47 (1990).
    • (1990) Ann. Hum. Genet. , vol.54 , pp. 39-47
    • Morton, N.E.1
  • 33
    • 0021637129 scopus 로고
    • Multilocus recombination frequencies
    • Morton, N.E. & Mactean, C.J. Multilocus recombination frequencies. Genet. Res. 44, 99-108 (1984).
    • (1984) Genet. Res. , vol.44 , pp. 99-108
    • Morton, N.E.1    Mactean, C.J.2
  • 34
    • 0025280026 scopus 로고
    • Centre d'Etude du Polymorphisme Humain (CEPH): Collaborative genetic mapping of the human genome
    • Dausset, J. et al. Centre d'Etude du Polymorphisme Humain (CEPH): Collaborative genetic mapping of the human genome. Genomics 6, 575-577 (1990).
    • (1990) Genomics , vol.6 , pp. 575-577
    • Dausset, J.1
  • 35
    • 0000803318 scopus 로고
    • Construction of multilocus genetic linkage maps in humans
    • Lander, E.S. & Green, P. Construction of multilocus genetic linkage maps in humans. Proc. Natl. Acad. Sci. USA 84, 2363-2367 (1987).
    • (1987) Proc. Natl. Acad. Sci. USA , vol.84 , pp. 2363-2367
    • Lander, E.S.1    Green, P.2
  • 36
    • 0024314891 scopus 로고
    • MAP, an expert system for multiple pairwise linkage analysis
    • Morton, N.E. & Andrews, V. MAP, an expert system for multiple pairwise linkage analysis. Ann. Hum. Genet. 53, 263-269 (1989).
    • (1989) Ann. Hum. Genet. , vol.53 , pp. 263-269
    • Morton, N.E.1    Andrews, V.2


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