An imprinted locus associated with transient neonatal diabetes mellitus

被引:165
作者
Gardner, RJ
Mackay, DJG
Mungall, AJ
Polychronakos, C
Siebert, R
Shield, JPH
Temple, IK
Robinson, DO [1 ]
机构
[1] Salisbury Dist Hosp, Wessex Reg Genet Lab, Salisbury SP2 8BJ, Wilts, England
[2] Sanger Ctr, Cambridge CB10 1SA, England
[3] Childrens Hosp, Res Inst, MTL, Quebec City, PQ H3Z 2Z3, Canada
[4] Univ Kiel, Dept Human Genet, D-24105 Kiel, Germany
[5] Princess Anne Hosp, Wessex Clin Genet Serv, Southampton SO16 5YA, Hants, England
[6] Inst Child Hlth, Bristol BS8 8BJ, Avon, England
关键词
D O I
10.1093/hmg/9.4.589
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recently, we reported the localization of a gene for transient neonatal diabetes mellitus (TNDM), a rare form of childhood diabetes, to an similar to 5.4 Mb region of chromosome 6q24. We have also shown that TNDM is associated with both paternal uniparental disomy (UPD) of chromosome 6 and paternal duplications of the critical region, The sequencing of P1-derived artificial chromosome clones from within the region of interest has allowed us to further localize the gene and to investigate the methylation status of the region.:The gene is now known to reside in a 300-400 kb region:of 6q24 which contains several CpG islands. At one island we have demonstrated differential DNA methylation between patients with paternal UPD of chromosome 6 and normal controls. In addition, two patients with TNDM, in whom neither paternal UPD of chromosome 6 nor duplication of 6q24 have been found, show a DNA methylation pattern identical to that of patients with paternal UPD of chromosome 6. Control individuals show a hemizygous methylation pattern, These results show that TNDM can be associated with a methylation change and identify a novel methylation imprint on chromosome 6 associated with TNDM.
引用
收藏
页码:589 / 596
页数:8
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