Mapping of the X-breakpoint involved in a balanced X;12 translocation in a female with mild mental retardation

被引:34
作者
Bienvenu, T
DerSarkissian, H
Billuart, P
Tissot, M
DesPortes, V
Bruls, T
Chabrolle, JP
Chauveau, P
Cherry, M
Kahn, A
Cohen, D
Beldjord, C
Chelly, J
Cherif, D
机构
[1] INSERM,U129,ICGM,FAC MED COCHIN,PARIS,FRANCE
[2] CTR ETUD POLYMORPHISME HUMAIN,F-75010 PARIS,FRANCE
[3] CTR HOSP HAVRE,LAB CYTOGENET,LE HAVRE,FRANCE
[4] CTR HOSP HAVRE,SERV MED NEONATALE,LE HAVRE,FRANCE
[5] CHU NANCY,LAB CYTOGENET,NANCY,FRANCE
关键词
mental retardation; translocation; fluorescent in situ hybridization; chromosome painting;
D O I
10.1159/000484743
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
Balanced chromosomal abnormalities such as translocations and inversions have been identified in many genetic diseases. Cloning of the breakpoints involved in these abnormalities has led to the identification of the disease-related genes. Recent reports suggest the presence of a mental retardation locus at Xq11-12. We have identified a female patient with a balanced translocation t(X;12)(q11;q15) associated with mild mental retardation. We identified a yeast artificial chromosome spanning the X-chromosome breakpoint by using fluorescent in situ hybridization techniques. A cosmid library of this YAC has been constructed and the search for candidate genes is in progress.
引用
收藏
页码:105 / 109
页数:5
相关论文
共 16 条
[1]   Identification by STS PCR screening of a microdeletion in Xp21.3-22.1 associated with non-specific mental retardation [J].
Billuart, P ;
Vinet, MC ;
Portes, VD ;
Llense, S ;
Richard, L ;
Moutard, ML ;
Recan, D ;
Bruls, T ;
Bienvenu, T ;
Kahn, A ;
Beldjord, C ;
Chelly, J .
HUMAN MOLECULAR GENETICS, 1996, 5 (07) :977-979
[2]   CHROMOSOME PAINTING IN ACUTE MONOCYTIC LEUKEMIA [J].
CHERIF, D ;
ROMANA, S ;
DERSARKISSIAN, H ;
JONES, C ;
BERGER, R .
GENES CHROMOSOMES & CANCER, 1993, 6 (02) :107-112
[3]   SIMULTANEOUS LOCALIZATION OF COSMIDS AND CHROMOSOME R-BANDING BY FLUORESCENCE MICROSCOPY - APPLICATION TO REGIONAL MAPPING OF HUMAN CHROMOSOME-11 [J].
CHERIF, D ;
JULIER, C ;
DELATTRE, O ;
DERRE, J ;
LATHROP, GM ;
BERGER, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (17) :6639-6643
[4]  
Davis Helen, 1996, European Journal of Human Genetics, V4, P91
[5]   HIGH-EFFICIENCY VECTORS FOR COSMID MICROCLONING AND GENOMIC ANALYSIS [J].
EVANS, GA ;
LEWIS, K ;
ROTHENBERG, BE .
GENE, 1989, 79 (01) :9-20
[6]   ASSIGNMENT OF THE GENE (EPLG2) ENCODING A HIGH-AFFINITY BINDING-PROTEIN FOR THE RECEPTOR TYROSINE KINASE ELK TO A 200-KILOBASEPAIR REGION IN HUMAN-CHROMOSOME XQ12 [J].
FLETCHER, FA ;
HUEBNER, K ;
SHAFFER, LG ;
FAIRWEATHER, ND ;
MONACO, AP ;
MULLER, U ;
DRUCK, T ;
SIMONEAUX, DK ;
CHELLY, J ;
BELMONT, JW ;
BECKMANN, MP ;
LYMAN, SD .
GENOMICS, 1995, 25 (01) :334-335
[7]   Identification of the gene FMR2, associated with FRAXE mental retardation [J].
Gecz, J ;
Gedeon, AK ;
Sutherland, GR ;
Mulley, JC .
NATURE GENETICS, 1996, 13 (01) :105-108
[8]  
Gedeon AK, 1996, AM J MED GENET, V64, P158, DOI 10.1002/(SICI)1096-8628(19960712)64:1<158::AID-AJMG26>3.3.CO
[9]  
2-V
[10]   SYNDROMAL MENTAL-RETARDATION DUE TO MUTATIONS IN A REGULATOR OF GENE-EXPRESSION [J].
GIBBONS, RJ ;
PICKETTS, DJ ;
HIGGS, DR .
HUMAN MOLECULAR GENETICS, 1995, 4 :1705-1709