Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas families

被引:18
作者
Laberge, S
Labauge, P
Maréchal, E
Maciazek, J
Tournier-Lasserve, E
机构
[1] Fac Med Necker, INSERM, U25, F-75730 Paris 15, France
[2] Hop Lariboisiere, F-75475 Paris, France
关键词
cavernous angiomas; chromosome; 7; founder effect; genetic heterogeneity;
D O I
10.1038/sj.ejhg.5200324
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cerebral cavernous angiomas malformations (CCM) can be inherited as an autosomal dominant condition. CCM1, a yet unidentified gene mapping on 7q21-q22, was shown to be involved in all CCM Hispano-American families, with a strong founder effect. Genetic heterogeneity in non Hispano-American families was established in two families. We conducted a genetic linkage analysis an 36 French CCM families using eight microsatellite markers mapping within the CCM1 interval, Admixture analysis showed that 65% of these families were linked to the CCM1 locus, Haplotypes analysis of CCM1-linked families did not show any evidence for a strong founder effect.
引用
收藏
页码:499 / 504
页数:6
相关论文
共 13 条
  • [1] DIB C, 1996, NATURE, V380, pA54
  • [2] A GENE RESPONSIBLE FOR CAVERNOUS MALFORMATIONS OF THE BRAIN MAPS TO CHROMOSOME 7Q
    DUBOVSKY, J
    ZABRAMSKI, JM
    KURTH, J
    SPETZLER, RF
    RICH, SS
    ORR, HT
    WEBER, JL
    [J]. HUMAN MOLECULAR GENETICS, 1995, 4 (03) : 453 - 458
  • [3] Familial cerebral cavernous angioma: A gene localized to a 15-cM interval on chromosome 7q
    GilNagel, A
    Dubovsky, J
    Wilcox, KJ
    Stewart, JM
    Anderson, VE
    Leppik, IE
    Orr, HT
    Johnson, EW
    Weber, JL
    Rich, SS
    [J]. ANNALS OF NEUROLOGY, 1996, 39 (06) : 807 - 810
  • [4] A founder mutation as a cause of cerebral cavernous malformation in Hispanic Americans
    Gunel, M
    Awad, IA
    Finberg, K
    Anson, JA
    Steinberg, GR
    Batjer, PH
    Kopitnik, TA
    Morrison, L
    Giannotta, SL
    NelsonWilliams, C
    Lifton, RP
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (15) : 946 - 951
  • [5] MAPPING A GENE CAUSING CEREBRAL CAVERNOUS MALFORMATION TO 7Q11.2-Q21
    GUNEL, M
    AWAD, IA
    ANSON, J
    LIFTON, RP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (14) : 6620 - 6624
  • [6] Gunel M, 1996, NEUROSURGERY, V38, P1265
  • [7] REFINED LOCALIZATION OF THE CEREBRAL CAVERNOUS MALFORMATION GENE (CCM1) TO A 4-CM INTERVAL OF CHROMOSOME 7Q CONTAINED IN A WELL-DEFINED YAC CONTIG
    JOHNSON, EW
    IYER, LM
    RICH, SS
    ORR, HT
    GILNAGEL, A
    KURTH, JH
    ZABRAMSKI, JM
    MARCHUK, DA
    WEISSENBACH, J
    CLERICUZIO, CL
    DAVIS, LE
    HART, BL
    GUSELLA, JF
    KOSOFSKY, BE
    LOUIS, DN
    MORRISON, LA
    GREEN, ED
    WEBER, JL
    [J]. GENOME RESEARCH, 1995, 5 (04) : 368 - 380
  • [8] Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families
    Labauge, P
    Laberge, S
    Brunereau, L
    Levy, C
    Tournier-Lasserve, E
    [J]. LANCET, 1998, 352 (9144) : 1892 - 1897
  • [9] A LOCUS FOR CEREBRAL CAVERNOUS MALFORMATIONS MAPS TO CHROMOSOME 7Q IN 2 FAMILIES
    MARCHUK, DA
    GALLIONE, CJ
    MORRISON, LA
    CLERICUZIO, CL
    HART, BL
    KOSOFSKY, BE
    LOUIS, DN
    GUSELLA, JF
    DAVIS, LE
    PRENGER, VL
    [J]. GENOMICS, 1995, 28 (02) : 311 - 314
  • [10] Familial cavernous malformations in a large French kindred: Mapping of the gene to the CCM1 locus on chromosome 7q
    Notelet, L
    Chapon, F
    Khoury, S
    Vahedi, K
    Chodkiewicz, JP
    Courtheoux, P
    IbaZizen, M
    Cabanis, EA
    Lechevalier, B
    TournierLasserve, E
    Houtteville, JP
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1997, 63 (01) : 40 - 45