The sequence and gene characterization of a 400-kb candidate region for IDDM4 on chromosome 11q13

被引:36
|
作者
Twells, RCJ
Metzker, ML
Brown, SD
Cox, R
Garey, C
Hammond, H
Hey, PJ
Levy, E
Nakagawa, Y
Philips, MS
Todd, JA
Hess, JF
机构
[1] Merck Res Labs, Dept Human Genet, W Point, PA 19486 USA
[2] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England
[3] Univ Cambridge, Dept Med Genet, Wellcome Trust Ctr Mol Mech Dis, Cambridge, England
关键词
D O I
10.1006/geno.2000.6492
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Type 1 diabetes is a complex disorder with interaction of both genetic and environmental factors, One of the loci, IDDM4, has been mapped to chromosome 11q13, with evidence of association to two markers, D11S1917 and H0570polyA. To identify putative candidate genes for IDDM4, we have constructed a 400-kb clone contig in this region and sequenced the clones. We have also sequenced the orthologous DNA from mouse. Previously, we identified a cDNA for the low-density lipoprotein receptor-related protein 5 gene (LRP5) 3 kb distal to H0570polyA. We have now determined the exon-intron structure of this gene. Detailed sequence analysis has identified a further three genes in this region: the CGI-85 gene (previously identified by W.-C, Lin) and two novel genes, C11orf24 and C11orf23. The C11orf24 gene has no known similarity to other genes, and its function is unknown. C11orf23 has similarity to the SIT4 (sporulation-induced transcript 4)-associated protein (SAP) family of yeast proteins, which are involved in regulation of the cell cycle. The full-length C11orf23 cDNA is the first mammalian orthologue of the yeast SAP family to be identified, Identification of these four genes in a 400-kb region of the IDDM4 region underpins our strategy to identify the IDDM4 locus. (C) 2001 Academic Press.
引用
收藏
页码:231 / 242
页数:12
相关论文
共 50 条
  • [31] Complete genomic sequence of the 471 kb Familial Dysautonomia candidate region on chromosome 9q31.
    Leyne, M
    Mull, J
    Gill, SP
    Liebert, CB
    Robbins, CM
    Pinkett, HW
    Makalowska, I
    Maayan, C
    Blumenfeld, A
    Axelrod, FB
    Brownstein, M
    Chadwick, BP
    Gusella, JF
    Slaugenhaupt, SA
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A92 - A92
  • [32] GENE AMPLIFICATION ON CHROMOSOME BAND 11Q13 AND ESTROGEN-RECEPTOR STATUS IN BREAST-CANCER
    FANTL, V
    RICHARDS, MA
    SMITH, R
    LAMMIE, GA
    JOHNSTONE, G
    ALLEN, D
    GREGORY, W
    PETERS, G
    DICKSON, C
    BARNES, DM
    EUROPEAN JOURNAL OF CANCER, 1990, 26 (04) : 423 - 429
  • [33] Generation and analysis of a BAC/PAC contig for the chromosome 15q11-q13 Autistic Disorder candidate gene region.
    Maddox, LO
    Menold, MM
    Zaeem, L
    Bass, MP
    Pericak-Vance, MA
    Vance, JM
    Gilbert, JR
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A459 - A459
  • [34] Deletion mapping of endocrine tumors localizes a second tumor suppressor gene on chromosome band 11q13
    Chakrabarti, R
    Srivatsan, ES
    Wood, TF
    Eubanks, PJ
    Ebrahimi, SA
    Gatti, RA
    Passaro, E
    Sawicki, MP
    GENES CHROMOSOMES & CANCER, 1998, 22 (02): : 130 - 137
  • [35] PEPSINOGEN GENE-COMPLEX (PGA) WAS ASSIGNED TO HUMAN-CHROMOSOME 11Q13 BY INSITU HYBRIDIZATION
    NAKAI, H
    HASEGAWA, K
    YAMAMOTO, Y
    TADA, K
    BYERS, MG
    SHOWS, TB
    TAGGART, RT
    JAPANESE JOURNAL OF HUMAN GENETICS, 1988, 33 (02): : 239 - 239
  • [36] THE INVOLVEMENT OF THE CHROMOSOME 11Q13 REGION IN HUMAN MALIGNANCIES - CYCLIN D1 AND EMS1 ARE 2 NEW CANDIDATE ONCOGENES - A REVIEW
    SCHUURING, E
    GENE, 1995, 159 (01) : 83 - 96
  • [37] Interactive effects between filaggrin gene and polymorphic variants on chromosome 11q13 for childhood eczema susceptibility
    Leung, T.
    Wang, S.
    Sy, H.
    Kong, A.
    Wong, G.
    Chan, J.
    Hon, K.
    ALLERGY, 2012, 67 : 80 - 80
  • [38] Fine mapping of a region of chromosome 11q13 reveals multiple independent loci associated with risk of prostate cancer
    Chung, Charles C.
    Ciampa, Julia
    Yeager, Meredith
    Jacobs, Kevin B.
    Berndt, Sonja I.
    Hayes, Richard B.
    Gonzalez-Bosquet, Jesus
    Kraft, Peter
    Wacholder, Sholom
    Orr, Nick
    Yu, Kai
    Hutchinson, Amy
    Boland, Joseph
    Chen, Quan
    Feigelson, Heather Spencer
    Thun, Michael J.
    Diver, W. Ryan
    Albanes, Demetrius
    Virtamo, Jarmo
    Weinstein, Stephanie
    Schumacher, Fredrick R.
    Cancel-Tassin, Geraldine
    Cussenot, Olivier
    Valeri, Antoine
    Andriole, Gerald L.
    Crawford, E. David
    Haiman, Christopher A.
    Henderson, Brian E.
    Kolonel, Laurence
    Le Marchand, Loic
    Siddiq, Afshan
    Riboli, Elio
    Key, Tim J.
    Kaaks, Rudolf
    Isaacs, William B.
    Isaacs, Sarah D.
    Gronberg, Henrik
    Wiklund, Fredrik
    Xu, Jianfeng
    Vatten, Lars J.
    Hveem, Kristian
    Njolstad, Inger
    Gerhard, Daniela S.
    Tucker, Margaret
    Hoover, Robert N.
    Fraumeni, Joseph F., Jr.
    Hunter, David J.
    Thomas, Gilles
    Chatterjee, Nilanjan
    Chanock, Stephen J.
    HUMAN MOLECULAR GENETICS, 2011, 20 (14) : 2869 - 2878
  • [39] Isolation and characterization of a novel gene close to the human phosphoinositide-specific phospholipase C beta 3 gene on chromosomal region 11q13
    Lagercrantz, J
    Carson, E
    Larsson, C
    Nordenskjold, M
    Weber, G
    GENOMICS, 1996, 31 (03) : 380 - 384
  • [40] Sporadic follicular thyroid tumors show loss of a 200-kb region in 11q13 without evidence for mutations in the MEN1 gene
    Nord, B
    Larsson, C
    Wong, FK
    Wallin, G
    Teh, BT
    Zedenius, J
    GENES CHROMOSOMES & CANCER, 1999, 26 (01): : 35 - 39