MUTATION HETEROGENEITY OF CYSTIC-FIBROSIS IN FRANCE - SCREENING BY DENATURING GRADIENT GEL-ELECTROPHORESIS USING PSORALEN-MODIFIED OLIGONUCLEOTIDE

被引:40
作者
BIENVENU, T
CAZENEUVE, C
KAPLAN, JC
BELDJORD, C
机构
[1] Laboratoire de Biochimie Génétique, Hôpital Cochin, Paris
关键词
CYSTIC FIBROSIS; MUTATIONS; DENATURING GRADIENT GEL ELECTROPHORESIS;
D O I
10.1002/humu.1380060106
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In order to establish counseling guidelines and aid carrier risk assessment, we sought to establish the frequencies of cystic fibrosis (CF) mutations that are present in CF families living in the Ile de France region, a region notable for its ethnic heterogeneity. We studied 470 CF chromosomes in which we identified more than 90% of the CF mutations. We systematically screened 21 exons and the adjacent sequences of the CF transmembrane conductance regulator (CFTR) gene by denaturing gradient gel electrophoresis using chemical clamps. We detected 41 different CF mutations located in 14 exons. One of these mutations had not been previously described. Given the heterogeneity of these mutations, population screening does not appear to be readily feasible in our population. (C) 1995 Wiley Liss, Inc.
引用
收藏
页码:23 / 29
页数:7
相关论文
共 37 条
  • [1] IDENTIFICATION OF 12 NOVEL MUTATIONS IN THE CFTR GENE
    AUDREZET, MP
    MERCIER, B
    GUILLERMIT, H
    QUERE, I
    VERLINGUE, C
    RAULT, G
    FEREC, C
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (01) : 51 - 54
  • [2] A NEW MISSENSE MUTATION (G27E) IN EXON-2 OF THE CFTR GENE IN A MILDLY AFFECTED CYSTIC-FIBROSIS PATIENT
    BIENVENU, T
    CAZENEUVE, C
    BELDJORD, C
    DUSSER, D
    KAPLAN, JC
    HUBERT, D
    [J]. HUMAN MOLECULAR GENETICS, 1994, 3 (02) : 365 - 366
  • [3] UNEXPECTED INACTIVATION OF ACCEPTOR CONSENSUS SPLICE SEQUENCE BY A -3C TO T-TRANSITION IN INTRON-2 OF THE CFTR GENE
    BIENVENU, T
    HUBERT, D
    FONKNECHTEN, N
    DUSSER, D
    KAPLAN, JC
    BELDJORD, C
    [J]. HUMAN GENETICS, 1994, 94 (01) : 65 - 68
  • [4] A MISSENSE MUTATION (F87L) IN EXON-3 OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR GENE
    BIENVENU, T
    PETITPRETZ, P
    BELDJORD, C
    KAPLAN, JC
    [J]. HUMAN MUTATION, 1994, 3 (04) : 395 - 396
  • [5] IDENTIFICATION OF A NEW FRAMESHIFT MUTATION (3724 DELG) IN EXON-19 OF THE CFTR GENE
    BIENVENU, T
    LENOIR, G
    FONKNECHTEN, N
    DESCLAUXARRAMOND, F
    KAPLAN, JC
    BELDJORD, C
    [J]. HUMAN MUTATION, 1994, 3 (01) : 69 - 70
  • [6] IDENTIFICATION OF 4 NEW MUTATIONS IN THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR GENE - I148T, L1077P, Y1092X, 2183AA-]G
    BOZON, D
    ZIELENSKI, J
    RININSLAND, F
    TSUI, LC
    [J]. HUMAN MUTATION, 1994, 3 (03) : 330 - 332
  • [7] 2 NOVEL FRAME-SHIFT MUTATIONS - 977-INSA IN EXON-6B, AND 4016-INST IN EXON-21, OF THE CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR (CFTR) GENE
    CHEADLE, JP
    ALJADER, LN
    MEREDITH, AL
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (03) : 317 - 319
  • [8] IDENTIFICATION OF A NEW MISSENSE MUTATION (P205S) IN THE 1ST TRANSMEMBRANE DOMAIN OF THE CFTR GENE ASSOCIATED WITH A MILD CYSTIC-FIBROSIS PHENOTYPE
    CHILLON, M
    CASALS, T
    NUNES, V
    GIMENEZ, J
    RUIZ, EP
    ESTIVILL, X
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (10) : 1741 - 1742
  • [9] ANALYSIS OF THE 27 EXONS AND FLANKING REGIONS OF THE CYSTIC-FIBROSIS GENE - 40 DIFFERENT MUTATIONS ACCOUNT FOR 91.2-PERCENT OF THE MUTANT ALLELES IN SOUTHERN FRANCE
    CLAUSTRES, M
    LAUSSEL, M
    DESGEORGES, M
    GIANSILY, M
    CULARD, JF
    RAZAKATSARA, G
    DEMAILLE, J
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (08) : 1209 - 1213
  • [10] PSORALEN-MODIFIED OLIGONUCLEOTIDE PRIMERS IMPROVE DETECTION OF MUTATIONS BY DENATURING GRADIENT GEL-ELECTROPHORESIS AND PROVIDE AN ALTERNATIVE TO GC-CLAMPING
    COSTES, B
    GIRODON, E
    GHANEM, N
    CHASSIGNOL, M
    THUONG, NT
    DUPRET, D
    GOOSSENS, M
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (04) : 393 - 397