Evidence of a novel type 2 diabetes locus 50 cM centromeric to NIDDM2 on chromosome 12q

被引:36
作者
Bektas, A
Suprenant, ME
Wogan, LT
Plengvidhya, N
Rich, SS
Warram, JH
Krolewski, AS
Doria, A
机构
[1] Joslin Diabet Ctr, Div Res, Sect Genet & Epidemiol, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[3] Wake Forest Univ, Sch Med, Winston Salem, NC 27109 USA
关键词
D O I
10.2337/diabetes.48.11.2246
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To replicate the recent finding of a type 2 diabetes locus (NIDDM2) on 12q, families segregating early-onset autosomal-dominant type 2 diabetes were screened for linkage. Included were 26 Caucasian and 6 non-Caucasian pedigrees with an average age at diabetes diagnosis of 37 +/- 18 years. Affected (n = 233) and nonaffected (n = 152) family members were genotyped for 17 markers covering 90 cM on chromosome 12q. While no evidence for linkage was detected at the NIDDM2 locus, a Linkage peak was observed 50 cM centromeric to NIDDM2 at markers D12S375 and D12S1052. In a nonparametric analysis, the Z(all) score was 2.9 (P = 0.015) at D12S375, and increased to 3.8 (P = 0.007) among Caucasian families. Further increase in significance was observed in pedigrees with poor insulin response, with a maximum Z(all) of 6.2 (P = 0.002) at D12S375. Suggestive evidence of linkage was also detected by the parametric analysis, with the heterogeneity logarithm of odds score peaking at 2.5 (alpha = 0.15) between D12S375 and D12S1052. In summary our data indicate that the NIDDM2 locus does not play a major role in early-onset autosomal-dominant type 2 diabetes. Rather, they strongly suggest that a previously undetected type 2 diabetes locus exists 50 cM from NIDDM2 on 12q.
引用
收藏
页码:2246 / 2251
页数:6
相关论文
共 19 条
  • [1] Comprehensive human genetic maps: Individual and sex-specific variation in recombination
    Broman, KW
    Murray, JC
    Sheffield, VC
    White, RL
    Weber, JL
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (03) : 861 - 869
  • [2] A physical map of 30,000 human genes
    Deloukas, P
    Schuler, GD
    Gyapay, G
    Beasley, EM
    Soderlund, C
    Rodriguez-Tomé, P
    Hui, L
    Matise, TC
    McKusick, KB
    Beckmann, JS
    Bentolila, S
    Bihoreau, MT
    Birren, BB
    Browne, J
    Butler, A
    Castle, AB
    Chiannilkulchai, N
    Clee, C
    Day, PJR
    Dehejia, A
    Dibling, T
    Drouot, N
    Duprat, S
    Fizames, C
    Fox, S
    Gelling, S
    Green, L
    Harrison, P
    Hocking, R
    Holloway, E
    Hunt, S
    Keil, S
    Lijnzaad, P
    Louis-Dit-Sully, C
    Ma, J
    Mendis, A
    Miller, J
    Morissette, J
    Muselet, D
    Nusbaum, HC
    Peck, A
    Rozen, S
    Simon, D
    Slonim, DK
    Staples, R
    Stein, LD
    Stewart, EA
    Suchard, MA
    Thangarajah, T
    Vega-Czarny, N
    [J]. SCIENCE, 1998, 282 (5389) : 744 - 746
  • [3] Phenotypic characteristics of early-onset autosomal-dominant type 2 diabetes unlinked to known maturity-onset diabetes of the young (MODY) genes
    Doria, A
    Yang, YD
    Malecki, M
    Scotti, S
    Dreyfus, J
    O'Keeffe, C
    Orban, T
    Warram, JH
    Krolewski, AS
    [J]. DIABETES CARE, 1999, 22 (02) : 253 - 261
  • [4] Ehm MG, 1999, DIABETES, V48, pA46
  • [5] Mutations in the hepatocyte nuclear factor-1 alpha gene are a common cause of maturity-onset diabetes of the young in the UK
    Frayling, TM
    Bulman, MP
    Ellard, S
    Appleton, M
    Dronsfield, MJ
    Mackle, ADR
    Baird, JD
    Kaisaki, PJ
    Yamagata, K
    Bell, GI
    Bain, SC
    Hattersley, AT
    [J]. DIABETES, 1997, 46 (04) : 720 - 725
  • [6] Type 2 diabetes: Evidence for linkage on chromosome 20 in 716 Finnish affected sib pairs
    Ghosh, S
    Watanabe, RM
    Hauser, ER
    Valle, T
    Magnuson, VL
    Erdos, MR
    Langefeld, CD
    Balow, J
    Ally, DS
    Kohtamaki, K
    Chines, P
    Birznieks, G
    Kaleta, HS
    Musick, A
    Te, C
    Tannenbaum, J
    Eldridge, W
    Shapiro, S
    Martin, C
    Witt, A
    So, A
    Chang, J
    Shurtleff, B
    Porter, R
    Kudelko, K
    Unni, A
    Segal, L
    Sharaf, R
    Blaschak-Harvan, J
    Eriksson, J
    Tenkula, T
    Vidgren, G
    Ehnholm, C
    Tuomilehto-Wolf, E
    Hagopian, W
    Buchanan, TA
    Tuomilehto, J
    Bergman, RN
    Collins, FS
    Boehnke, M
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) : 2198 - 2203
  • [7] A genome-wide search for human non-insulin dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2
    Hanis, CL
    Boerwinkle, E
    Chakraborty, R
    Ellsworth, DL
    Concannon, P
    Stirling, B
    Morrison, VA
    Wapelhorst, B
    Spielman, RS
    GogolinEwens, KJ
    Shephard, JM
    Williams, SR
    Risch, N
    Hinds, D
    Iwasaki, N
    Ogata, M
    Omori, Y
    Petzold, C
    Rietzsch, H
    Schroder, HE
    Schulze, J
    Cox, NJ
    Menzel, S
    Boriraj, VV
    Chen, X
    Lim, LR
    Lindner, T
    Mereu, LE
    Wang, YQ
    Xiang, K
    Yamagata, K
    Yang, Y
    Bell, GI
    [J]. NATURE GENETICS, 1996, 13 (02) : 161 - 166
  • [8] IMPAIRED GLUCOSE-TOLERANCE IN THE UNITED-STATES POPULATION
    HARRIS, MI
    [J]. DIABETES CARE, 1989, 12 (07) : 464 - 474
  • [9] Generation and analysis of 280,000 human expressed sequence tags
    Hillier, L
    Lennon, G
    Becker, M
    Bonaldo, MF
    Chiapelli, B
    Chissoe, S
    Dietrich, N
    DuBuque, T
    Favello, A
    Gish, W
    Hawkins, M
    Hultman, M
    Kucaba, T
    Lacy, M
    Le, M
    Le, N
    Mardis, E
    Moore, B
    Morris, M
    Parsons, J
    Prange, C
    Rifkin, L
    Rohlfing, T
    Schellenberg, K
    Soares, MB
    Tan, F
    ThierryMeg, J
    Trevaskis, E
    Underwood, K
    Wohldman, P
    Waterston, R
    Wilson, R
    Marra, M
    [J]. GENOME RESEARCH, 1996, 6 (09) : 807 - 828
  • [10] Kruglyak L, 1996, AM J HUM GENET, V58, P1347