Exclusion of ZFM1 as a candidate gene for multiple endocrine neoplasia type 1 (MEN1)

被引:0
|
作者
S. E. Lloyd
J. T. Pang
S. H. S. Pearce
S. E. A. Leigh
R. V. Thakker
机构
[1] MRC Molecular Endocrinology Group,
[2] MRC Clinical Sciences Centre,undefined
[3] Royal Postgraduate Medical School,undefined
[4] Hammersmith Hospital,undefined
[5] Du Cane Road,undefined
[6] London W12 ONN,undefined
[7] UK Tel.: +44 181 383 3014; Fax: +44 181 383 8306 e-mail: rthakker@rpms.ac.uk,undefined
来源
Human Genetics | 1997年 / 99卷
关键词
Candidate Gene; Zinc Finger; Nuclear Localisation Signal; Proline Residue; Zinc Finger Motif;
D O I
暂无
中图分类号
学科分类号
摘要
The multiple endocrine neoplasia type 1 (MEN1) locus has been previously localised to 11q13 by combined tumour deletion mapping and linkage studies and a 3.8-cM region flanked by PYGM and D11S97 has been defined. The zinc finger in the MEN1 locus (ZFM1) gene, which has also been mapped to this region, represents a candidate gene for MEN1. The ZFM1 gene, which consists of 14 exons, encodes a 623-amino acid protein and exons 2, 8 and 12 encode the putative nuclear localisation signal, a zinc finger motif, and a proline-rich region, respectively. We have investigated these potentially functional regions for germ-line mutations by single-stranded conformational polymorphism (SSCP) analysis in 64 unrelated MEN1 patients. In addition, we performed DNA sequence analysis of all the 14 exons and 13 of the 26 exon-intron boundaries in four unrelated MEN1 patients. A 6-bp deletion that resulted in the loss of two proline residues at codons 479 and 480 in exon 12 was found in one MEN1 patient. However, this did not co-segregate with MEN1 in the family and represented a rare polymorphism. Analysis by SSCP, DNA sequencing, northern blotting, Southern blotting and pulsed field gel electrophoresis revealed no additional genetic abnormalities of ZFM1 in the other MEN1 patients. Thus, our results indicate that ZFM1 is excluded as a candidate gene for MEN1.
引用
收藏
页码:585 / 589
页数:4
相关论文
共 50 条
  • [41] Multiple endocrine neoplasia type 1 (MEN1): Not only inherited endocrine tumors
    Falchetti, Alberto
    Marini, Francesca
    Luzi, Ettore
    Giusti, Francesca
    Cavalli, Loredana
    Cavalli, Tiziana
    Brandi, Maria Luisa
    GENETICS IN MEDICINE, 2009, 11 (12) : 825 - 835
  • [42] MEN1 gene mutation analysis in Italian patients with multiple endocrine neoplasia type 1
    Morelli, A
    Falchetti, A
    Martineti, V
    Becherini, L
    Mark, W
    Friedman, E
    Brandi, ML
    EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2000, 142 (02) : 131 - 137
  • [43] Germline mutations of the MEN1 gene in Japanese kindred with multiple endocrine neoplasia type 1
    Shimizu, S
    Tsukada, T
    Futami, H
    Ui, K
    Kameya, T
    Kawanaka, M
    Uchiyama, S
    Aoki, A
    Yasuda, H
    Kawano, S
    Ito, Y
    Kanbe, M
    Obara, T
    Yamaguchi, K
    JAPANESE JOURNAL OF CANCER RESEARCH, 1997, 88 (11): : 1029 - 1032
  • [44] Germline mutations of the MEN1 gene in Korean families with multiple endocrine neoplasia type 1 (MEN1) or MEN1-related disorders
    Park, JH
    Kim, IJ
    Kang, HC
    Lee, SH
    Shin, Y
    Kim, KH
    Lim, SB
    Kang, SB
    Lee, K
    Kim, SY
    Lee, MS
    Lee, MK
    Park, JH
    Moon, SD
    Park, JG
    CLINICAL GENETICS, 2003, 64 (01) : 48 - 53
  • [45] Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4)
    Thakker, Rajesh V.
    MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2014, 386 (1-2) : 2 - 15
  • [46] Germline MEN1 mutations in sixteen Japanese families with multiple endocrine neoplasia type 1 (MEN1)
    Hai, N
    Aoki, N
    Matsuda, A
    Mori, T
    Kosugi, S
    EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1999, 141 (05) : 475 - 480
  • [47] No evidence of germline mutation or somatic deletion of the MEN1 gene in a case of familial multiple endocrine neoplasia type 1 (MEN1)
    Namihira, H
    Sato, M
    Matsubara, S
    Ohye, H
    Bhuiyan, MMR
    Murao, K
    Takahara, J
    ENDOCRINE JOURNAL, 1999, 46 (06) : 811 - 816
  • [48] The European Consortium on MEN1 - Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1)
    Bassett, JHD
    Pannett, AAJ
    Forbes, SA
    Thakker, RV
    McCarthy, M
    Read, AP
    Teh, BT
    Larsson, C
    Kytola, S
    Leisti, J
    Salmela, P
    Weber, G
    Giraud, S
    Zhang, CX
    Calender, A
    Hoppener, JWM
    vanAmstel, HKP
    Lips, CJM
    Kas, K
    VandeVen, WJM
    Gaudray, P
    HUMAN GENETICS, 1997, 100 (5-6) : 657 - 665
  • [49] Identification of five novel germline mutations of the MEN1 gene in Japanese multiple endocrine neoplasia type 1 (MEN1) families
    Sato, M
    Matsubara, S
    Miyauchi, A
    Ohye, H
    Imachi, H
    Murao, K
    Takahara, J
    JOURNAL OF MEDICAL GENETICS, 1998, 35 (11) : 915 - 919
  • [50] A novel germline mutation of multiple endocrine neoplasia type 1 (MEN1) gene in a Japanese MEN1 patient and her daughter
    Ohye, H
    Sato, M
    Matsubara, S
    Miyauchi, A
    Kishi-Imai, K
    Murao, K
    Takahara, J
    ENDOCRINE JOURNAL, 1999, 46 (02) : 325 - 329