The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic cases

被引:57
作者
Rose, CSP
Patel, P
Reardon, W
Malcolm, S
Winter, RM
机构
[1] INST CHILD HLTH,MOL GENET UNIT,LONDON WC1N 1EH,ENGLAND
[2] INST CHILD HLTH,CLIN GENET UNIT,LONDON WC1N 1EH,ENGLAND
关键词
D O I
10.1093/hmg/6.8.1369
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
The TWIST gene maps to 7p21 and mutations in the gene have been reported in the Saethre-Chotzen form of craniosynostosis, The position of the Saethre-Chotzen gene has previously been refined by FISH analysis of four patients carrying balanced translocations involving 7p21 which suggested that it was located between D7S488 and D7S503, We report here that the breakpoints in four translocation patients do not interrupt the coding sequence of the TWIST gene and thus most likely act through a positional effect, Twelve Saethre-Chotzen cases were found to have TWIST mutations. Four of these families had been used as part of the linkage study of the Saethre-Chotzen locus, The mutations detected included missense and nonsense mutations and three cases of a 21 bp duplication. Although phenotypically diagnosed as having Saethre-Chotzen syndrome, three families were found to have a pro250arg mutation of FGFR3.
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页码:1369 / 1373
页数:5
相关论文
共 21 条
  • [1] Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes
    Bellus, GA
    Gaudenz, K
    Zackai, EH
    Clarke, LA
    Szabo, J
    Francomano, CA
    Muenke, M
    [J]. NATURE GENETICS, 1996, 14 (02) : 174 - 176
  • [2] THE MAPPING OF A GENE FOR CRANIOSYNOSTOSIS - EVIDENCE FOR LINKAGE OF THE SAETHRE-CHOTZEN SYNDROME TO DISTAL CHROMOSOME-7P
    BRUETON, LA
    VANHERWERDEN, L
    CHOTAI, KA
    WINTER, RM
    [J]. JOURNAL OF MEDICAL GENETICS, 1992, 29 (10) : 681 - 685
  • [3] 6 CASES OF 7P DELETION - CLINICAL, CYTOGENETIC, AND MOLECULAR STUDIES
    CHOTAI, KA
    BRUETON, LA
    VANHERWERDEN, L
    GARRETT, C
    HINKEL, GK
    SCHINZEL, A
    MUELLER, RF
    SPELEMAN, F
    WINTER, RM
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 51 (03): : 270 - 276
  • [4] Characterization of the split hand split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development
    Crackower, MA
    Scherer, SW
    Rommens, JM
    Hui, CC
    Poorkaj, P
    Soder, S
    Cobben, JM
    Hudgins, L
    Evans, JP
    Tsui, LC
    [J]. HUMAN MOLECULAR GENETICS, 1996, 5 (05) : 571 - 579
  • [5] ASSOCIATION BETWEEN X-LINKED MIXED DEAFNESS AND MUTATIONS IN THE POU DOMAIN GENE POU3F4
    DEKOK, YJM
    VANDERMAAREL, SM
    BITNERGLINDZICZ, M
    HUBER, I
    MONACO, AP
    MALCOLM, S
    PEMBREY, ME
    ROPERS, HH
    CREMERS, FPM
    [J]. SCIENCE, 1995, 267 (5198) : 685 - 688
  • [6] A comprehensive genetic map of the human genome based on 5,264 microsatellites
    Dib, C
    Faure, S
    Fizames, C
    Samson, D
    Drouot, N
    Vignal, A
    Millasseau, P
    Marc, S
    Hazan, J
    Seboun, E
    Lathrop, M
    Gyapay, G
    Morissette, J
    Weissenbach, J
    [J]. NATURE, 1996, 380 (6570) : 152 - 154
  • [7] ElGhouzzi V, 1997, NAT GENET, V15, P42
  • [8] Transcription factors in disease
    Engelkamp, D
    vanHeyningen, V
    [J]. CURRENT OPINION IN GENETICS & DEVELOPMENT, 1996, 6 (03) : 334 - 342
  • [9] Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome
    Howard, TD
    Paznekas, WA
    Green, ED
    Chiang, LC
    Ma, N
    DeLuna, RIO
    Delgado, CG
    GonzalezRamos, M
    Kline, AD
    Jabs, EW
    [J]. NATURE GENETICS, 1997, 15 (01) : 36 - 41
  • [10] GENETIC-HETEROGENEITY AMONG CRANIOSYNOSTOSIS SYNDROMES - MAPPING THE SAETHRE-CHOTZEN SYNDROME LOCUS BETWEEN D7S513 AND D7S516 AND EXCLUSION OF JACKSON-WEISS AND CROUZON SYNDROME LOCI FROM 7P
    LEWANDA, AF
    COHEN, MM
    JACKSON, CE
    TAYLOR, EW
    LI, X
    BELOFF, M
    DAY, D
    CLARREN, SK
    ORTIZ, R
    GARCIA, C
    HAUSELMAN, E
    FIGUEROA, A
    WULFSBERG, E
    WILSON, M
    WARMAN, ML
    PADWA, BL
    WHITEMAN, DAH
    MULLIKEN, JB
    JABS, EW
    [J]. GENOMICS, 1994, 19 (01) : 115 - 119