Gap junction beta 1 (GJB1) gene mutations in Italian patients with X-linked Charcot-Marie-Tooth disease

被引:17
作者
Mandich, Paola [1 ]
Grandis, Marina [2 ]
Geroldi, Alessandro [1 ]
Acquaviva, Massimo [1 ]
Varese, Alessandra [1 ]
Gulli, Rossella [1 ]
Ciotti, Paola [1 ]
Bellone, Emilia [1 ]
机构
[1] Univ Genoa, Dept Neurosci Ophthalmol & Genet, Med Genet Sect, DIMI, I-16132 Genoa, Italy
[2] Univ Genoa, Dept Neurosci Ophthalmol & Genet, Sect Neurol & Neurol Rehabil, I-16132 Genoa, Italy
关键词
X-linked Charcot-Marie-Tooth disease; Connexin32 (Cx32); GJB1; mutation; Italian;
D O I
10.1007/s10038-008-0280-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
X-linked Charcot-Marie-Tooth disease (CMT1X) is a peripheral neuropathy transmitted in a dominant manner and caused by mutations in the Connexin 32 (Cx32) gene (GJB1, gap junction beta 1). Here we report the mutation analysis of the GJB1 gene in 76 subjects with possible CMT1 and absence of 17p11.2 duplication, and in 38 CMT2 patients without mutations in CMT2-associated-genes, selected from a cohort of 684 patients with peripheral sensory-motor neuropathy. The analysis was performed by direct sequencing of the coding sequence and exon/intron boundaries of the GJB1 gene. The mutation screening identified 22 mutations in GJB1, eight of which have not been previously published: six point mutations (c.50C > G, c.107T > A, c.545C > T, c.545C > G, c.548G > C, c.791G > T) and two deletions (c.84delC, c.573_581delCGTCTTCAT). The GJB1 mutation frequency (19.3%) and the clinical heterogeneity of our patients suggest searching for GJB1 mutations in all CMT cases without the 17p11.2 duplication, regardless of the gender of the proband, as well as in CMT2 patients with possible X-linked inheritance.
引用
收藏
页码:529 / 533
页数:5
相关论文
共 35 条
  • [1] [Anonymous], 1998, Neuromuscul Disord, V8, P591, DOI 10.1016/S0960-8966(98)00067-4
  • [2] Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin32 gene
    Bähr, M
    Andres, F
    Timmerman, V
    Nelis, ME
    Van Broeckhoven, C
    Dichgans, J
    [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1999, 66 (02) : 202 - 206
  • [3] Functional gap junctions in the Schwann cell myelin sheath
    Balice-Gordon, RJ
    Bone, LJ
    Scherer, SS
    [J]. JOURNAL OF CELL BIOLOGY, 1998, 142 (04) : 1095 - 1104
  • [4] CONNEXIN MUTATIONS IN X-LINKED CHARCOT-MARIE-TOOTH DISEASE
    BERGOFFEN, J
    SCHERER, SS
    WANG, S
    SCOTT, MO
    BONE, LJ
    PAUL, DL
    CHEN, K
    LENSCH, MW
    CHANCE, PF
    FISCHBECK, KH
    [J]. SCIENCE, 1993, 262 (5142) : 2039 - 2042
  • [5] Connexin32 and X-linked Charcot-Marie-Tooth disease
    Bone, LJ
    Deschenes, SM
    BaliceGordon, RJ
    Fischbeck, KH
    Scherer, SS
    [J]. NEUROBIOLOGY OF DISEASE, 1997, 4 (3-4) : 221 - 230
  • [6] Clinical and molecular analysis of X-linked Charcot-Marie-Tooth disease type 1 in Spanish population
    Casasnovas, C.
    Banchs, I.
    Corral, J.
    Martinez-Matos, J. A.
    Volpini, V.
    [J]. CLINICAL GENETICS, 2006, 70 (06) : 516 - 523
  • [7] MUTATIONS IN THE CONNEXIN-32 GENE IN X-LINKED DOMINANT CHARCOT-MARIE-TOOTH DISEASE (CMTX1)
    FAIRWEATHER, N
    BELL, C
    COCHRANE, S
    CHELLY, J
    WANG, S
    MOSTACCIUOLO, ML
    MONACO, AP
    HAITES, NE
    [J]. HUMAN MOLECULAR GENETICS, 1994, 3 (01) : 29 - 34
  • [8] Flagiello Luisa, 1998, Human Mutation, V12, P361
  • [9] Gutierrez A, 2000, MUSCLE NERVE, V23, P182, DOI 10.1002/(SICI)1097-4598(200002)23:2<182::AID-MUS6>3.0.CO
  • [10] 2-W