Transient neonatal diabetes, a disorder of imprinting

被引:152
作者
Temple, IK
Shield, JPH
机构
[1] Southampton Univ Hosp, NHS Trust, Wessex Clin Genet Serv, Southampton SO16 5YA, Hants, England
[2] Bristol Royal Hosp Children, Dept Child Hlth, Bristol BS2 8BJ, Avon, England
关键词
D O I
10.1136/jmg.39.12.872
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Transient neonatal diabetes (TND) is a rare but distinct type of diabetes. Classically, neonates present with growth retardation and diabetes in the first week of life. Apparent remission occurs by 3 months but there is a tendency for children to develop diabetes in later life. Evidence suggests it is the result of overexpression of an imprinted and paternally expressed gene/s within the TND critical region at 6q24. Two imprinted genes, ZAC (zinc finger protein associated with apoptosis and cell cycle arrest) and HYMAI (imprinted in hydatidiform mole) have been identified as potential candidates. Three genetic mechanisms have been shown to result in TND, paternal uniparental isodisomy of chromosome 6, paternally inherited duplication of 6q24, and a methylation defect at a CpG island overlapping exon 1 of ZAC/HYMAI.
引用
收藏
页码:872 / 875
页数:4
相关论文
共 44 条
  • [1] ISODISOMY OF CHROMOSOME-6 IN A NEWBORN WITH METHYLMALONIC ACIDEMIA AND AGENESIS OF PANCREATIC BETA-CELLS CAUSING DIABETES-MELLITUS
    ABRAMOWICZ, MJ
    ANDRIEN, M
    DUPONT, E
    DORCHY, H
    PARMA, J
    DUPREZ, L
    LEDLEY, FD
    COURTENS, W
    VAMOS, E
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (01) : 418 - 421
  • [2] A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus
    Arima, T
    Drewell, RA
    Arney, KL
    Inoue, J
    Makita, Y
    Hata, A
    Oshimura, M
    Wake, N
    Surani, MA
    [J]. HUMAN MOLECULAR GENETICS, 2001, 10 (14) : 1475 - 1483
  • [3] A novel imprinted gene, HYMAI, is located within an imprinted domain on human chromosome 6 containing ZAC
    Arima, T
    Drewell, RA
    Oshimura, M
    Wake, N
    Surani, MA
    [J]. GENOMICS, 2000, 67 (03) : 248 - 255
  • [5] Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse
    Brunkow, ME
    Jeffery, EW
    Hjerrild, KA
    Paeper, B
    Clark, LB
    Yasayko, SA
    Wilkinson, JE
    Galas, D
    Ziegler, SF
    Ramsdell, F
    [J]. NATURE GENETICS, 2001, 27 (01) : 68 - 73
  • [6] Refinement of the 6q chromosomal region implicated in transient neonatal diabetes
    Cavé, H
    Polak, M
    Drunat, S
    Denamur, E
    Czernichow, P
    [J]. DIABETES, 2000, 49 (01) : 108 - 113
  • [7] DISTINCT NEUROLOGICAL SYNDROME IN 2 BROTHERS WITH HYPERURICEMIA
    CHRISTEN, HJ
    HANEFELD, F
    DULEY, JA
    SIMMONDS, HA
    [J]. LANCET, 1992, 340 (8828) : 1167 - 1168
  • [8] Induction of the PAC1-R (PACAP-type I receptor) gene by p53 and Zac
    Ciani, E
    Hoffmann, A
    Schmidt, P
    Journot, L
    Spengler, D
    [J]. MOLECULAR BRAIN RESEARCH, 1999, 69 (02): : 290 - 294
  • [9] TRANSIENT NOENATAL DIABETES MELLITUS IN HALF SISTERS
    COFFEY, JD
    WOMACK, NC
    [J]. AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1967, 113 (04): : 480 - +
  • [10] Cornblath M, 1966, DISORDERS CARBOHYDRA, V3, P105