17Q INVERSION INVOLVING THE NEUROFIBROMATOSIS TYPE ONE LOCUS IN A FAMILY WITH NEUROFIBROMATOSIS TYPE ONE

被引:4
作者
ASAMOAH, A
NORTH, K
DORAN, S
WAGSTAFF, J
OGLE, R
COLLINS, FS
KORF, BR
机构
[1] CHILDRENS HOSP,DIV GENET,BOSTON,MA 02115
[2] CHILDRENS HOSP,DEPT GENET,SYDNEY,NSW,AUSTRALIA
[3] NATL CTR HUMAN GENOME RES,ANN ARBOR,MI
[4] UNIV MICHIGAN,ANN ARBOR,MI 48109
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 60卷 / 04期
关键词
PARACENTRIC INVERSION; CHROMOSOMES; FLUORESCENCE IN SITU HYBRIDIZATION; FIELD INVERSION GEL ELECTROPHORESIS; MUTATION;
D O I
10.1002/ajmg.1320600410
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report a family with a paracentric inversion of the long arm of chromosome 17 [inv(17)(q11.2q25.1)] and neurofibromatosis type one (NF1), The family was ascertained because of NF1 and multiple miscarriages. Fluorescence in situ hybridization using cosmid probes from opposite ends of the NF1 gene confirmed that the inversion disrupts the gene, Using field inversion gel electrophoresis we have found that the inversion separates cDNA probes FB5D and AE25, which are normally adjacent to one another in the NF1 gene. This is the third published report of a gross chromosomal rearrangement responsible for NF1, The features in this family are typical for NF1, and are not unusually severe. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:312 / 316
页数:5
相关论文
共 27 条
  • [11] LEDBETTER DH, 1989, AM J HUM GENET, V44, P20
  • [12] FLUORESCENCE INSITU HYBRIDIZATION WITH ALU AND L1 POLYMERASE CHAIN-REACTION PROBES FOR RAPID CHARACTERIZATION OF HUMAN-CHROMOSOMES IN HYBRID CELL-LINES
    LICHTER, P
    LEDBETTER, SA
    LEDBETTER, DH
    WARD, DC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (17) : 6634 - 6638
  • [13] CDNA CLONING OF THE TYPE-1 NEUROFIBROMATOSIS GENE - COMPLETE SEQUENCE OF THE NF1 GENE-PRODUCT
    MARCHUK, DA
    SAULINO, AM
    TAVAKKOL, R
    SWAROOP, M
    WALLACE, MR
    ANDERSEN, LB
    MITCHELL, AL
    GUTMANN, DH
    BOGUSKI, M
    COLLINS, FS
    [J]. GENOMICS, 1991, 11 (04) : 931 - 940
  • [14] OCONNELL P, 1989, AM J HUM GENET, V44, P51
  • [15] 2 NF1 TRANSLOCATIONS MAP WITHIN A 600-KILOBASE SEGMENT OF 17Q11.2
    OCONNELL, P
    LEACH, R
    CAWTHON, RM
    CULVER, M
    STEVENS, J
    VISKOCHIL, D
    FOURNIER, REK
    RICH, DC
    LEDBETTER, DH
    WHITE, R
    [J]. SCIENCE, 1989, 244 (4908) : 1087 - 1088
  • [16] RICCARDI VM, 1993, AM J HUM GENET, V53, P301
  • [17] SIMULTANEOUS VISUALIZATION OF 7 DIFFERENT DNA PROBES BY INSITU HYBRIDIZATION USING COMBINATORIAL FLUORESCENCE AND DIGITAL IMAGING MICROSCOPY
    RIED, T
    BALDINI, A
    RAND, TC
    WARD, DC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (04) : 1388 - 1392
  • [18] CASES OF NEUROFIBROMATOSIS WITH REARRANGEMENTS OF CHROMOSOME-17 INVOLVING BAND 17Q11.2
    SCHMIDT, MA
    MICHELS, VV
    DEWALD, GW
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 28 (03): : 771 - 777
  • [19] GENETIC-LINKAGE OF VONRECKLINGHAUSEN NEUROFIBROMATOSIS TO THE NERVE GROWTH-FACTOR RECEPTOR GENE
    SEIZINGER, BR
    ROULEAU, GA
    OZELIUS, LJ
    LANE, AH
    FARYNIARZ, AG
    CHAO, MV
    HUSON, S
    KORF, BR
    PARRY, DM
    PERICAKVANCE, MA
    COLLINS, FS
    HOBBS, WJ
    FALCONE, BG
    IANNAZZI, JA
    ROY, JC
    STGEORGEHYSLOP, PH
    TANZI, RE
    BOTHWELL, MA
    UPADHYAYA, M
    HARPER, P
    GOLDSTEIN, AE
    HOOVER, DL
    BADER, JL
    SPENCE, MA
    MULVIHILL, JJ
    AYLSWORTH, AS
    VANCE, JM
    ROSSENWASSER, GOD
    GASKELL, PC
    ROSES, AD
    MARTUZA, RL
    BREAKEFIELD, XO
    GUSELLA, JF
    [J]. CELL, 1987, 49 (05) : 589 - 594
  • [20] NEUROFIBROMATOSIS TYPE-1 (NF1) - THE SEARCH FOR MUTATIONS BY PCR-HETERODUPLEX ANALYSIS ON HYDROLINK GELS
    SHEN, MH
    HARPER, PS
    UPADHYAYA, M
    [J]. HUMAN MOLECULAR GENETICS, 1993, 2 (11) : 1861 - 1864