High-resolution map and imprinting analysis of the Gtl2-Dnchc1 domain on mouse chromosome 12

被引:99
作者
Tierling, S
Dalbert, S
Schoppenhorst, S
Tsai, CE
Oliger, S
Ferguson-Smith, AC
Paulsen, M
Walter, J
机构
[1] Univ Saarland, FR Biowissensch 8 3, D-66041 Saarbrucken, Germany
[2] Univ Cambridge, Dept Anat, Cambridge CB2 3DY, England
基金
英国医学研究理事会;
关键词
imprinting; DNA methylation; Gtl2; Mirg; Ppp2r5c; Dnchc1;
D O I
10.1016/j.ygeno.2005.09.018
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
The imprinted Dlk1 -Dio3 region on mouse chromosome 12 contains six imprinted genes and a number of maternally expressed snoRNAs and miRNAs. Here we present a high-resolution sequence analysis of the 1.1-Mb segment telomeric to Gtl2 in mouse and a homology comparison to the human. Ppp2r5c and Dnchc1 at the telomeric end of the analyzed sequence are biallelically expressed, suggesting that the imprinted domain does not extend beyond the paternally expressed Dio3 gene. RT-PCR experiments support the predicted presence of a maternally expressed intergenic transcript(s) encompassing Gtl2, Rian, and Mirg. These maternally expressed genes, and also the intergenic transcript(s), show pronounced expression in the adult mouse brain, whereas the paternally transcribed Dio3 and the nonimprinted Ppp2r5c and Dnchc1 are expressed in different tissues. Hence, tissue-specific coregulation of maternally expressed genes might be an important feature of this domain. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:225 / 235
页数:11
相关论文
共 36 条
  • [1] ExQuest, a novel method for displaying quantitative gene expression from ESTs
    Brown, AC
    Kai, K
    May, ME
    Brown, DC
    Roopenian, DC
    [J]. GENOMICS, 2004, 83 (03) : 528 - 539
  • [2] Identification of tandemly-repeated C/D snoRNA genes at the imprinted human 14q32 domain reminiscent of those at the Prader-Willi/Angelman syndrome region
    Cavaillé, J
    Seitz, H
    Paulsen, M
    Ferguson-Smith, AC
    Bachellerie, JP
    [J]. HUMAN MOLECULAR GENETICS, 2002, 11 (13) : 1527 - 1538
  • [3] Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
    Cavaillé, J
    Buiting, K
    Kiefmann, M
    Lalande, M
    Brannan, CI
    Horsthemke, B
    Bachellerie, JP
    Brosius, J
    Hüttenhofer, A
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (26) : 14311 - 14316
  • [4] The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status
    Charlier, C
    Segers, K
    Karim, L
    Shay, T
    Gyapay, G
    Cockett, N
    Georges, M
    [J]. NATURE GENETICS, 2001, 27 (04) : 367 - 369
  • [5] CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
  • [6] MULTIPLE SEQUENCE ALIGNMENT WITH HIERARCHICAL-CLUSTERING
    CORPET, F
    [J]. NUCLEIC ACIDS RESEARCH, 1988, 16 (22) : 10881 - 10890
  • [7] Increased plasticity of genomic imprinting of Dlk1 in brain is due to genetic and epigenetic factors
    Croteau, S
    Roquis, D
    Charron, MC
    Frappier, D
    Yavin, D
    Loredo-Osti, JC
    Hudson, TJ
    Naumova, AK
    [J]. MAMMALIAN GENOME, 2005, 16 (02) : 127 - 135
  • [8] RNAi-mediated allelic trans-interaction at the imprinted Rtl1/Peg11 locus
    Davis, E
    Caiment, F
    Tordoir, X
    Cavaillé, J
    Ferguson-Smith, A
    Cockett, N
    Georges, M
    Charlier, C
    [J]. CURRENT BIOLOGY, 2005, 15 (08) : 743 - 749
  • [9] El-Maarri Osman, 2004, Methods Mol Biol, V287, P195
  • [10] The callipyge locus:: evidence for the trans interaction of reciprocally imprinted genes
    Georges, M
    Charlier, C
    Cockett, N
    [J]. TRENDS IN GENETICS, 2003, 19 (05) : 248 - 252