Isolation and initial characterization of a novel zinc finger gene, DNMT3L, on 21q22.3, related to the cytosine-5-methyltransferase 3 gene family

被引:205
作者
Aapola, U
Shibuya, K
Scott, HS
Ollila, J
Vihinen, M
Heino, M
Shintani, A
Kawasaki, K
Minoshima, S
Krohn, K
Antonarakis, SE
Shimizu, N
Kudoh, J
Peterson, P
机构
[1] Univ Tampere, Inst Med Technol, Dept Pathol, FIN-33101 Tampere, Finland
[2] Tampere Univ Hosp, Tampere 33520, Finland
[3] Keio Univ, Sch Med, Dept Mol Biol, Shinjuku Ku, Tokyo 1608582, Japan
[4] Univ Geneva, Sch Med, Div Med Genet, CH-1211 Geneva, Switzerland
[5] Univ Hosp Geneva, Div Med Genet, Geneva, Switzerland
[6] Univ Helsinki, Dept Biosci, Div Biochem, FIN-00014 Helsinki, Finland
基金
日本科学技术振兴机构; 芬兰科学院; 日本学术振兴会;
关键词
D O I
10.1006/geno.2000.6168
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
We have isolated the DNMT3L gene that is related to the cytosine-5-methyltransferase 3 (DNMT3) family. The gene is located on chromosome 21q22.3 between the AIRE and the KIAA0653 genes and spans approximately 16 kb of genomic sequence. The encoded protein of 387 amino acids has a cysteine-rich region containing a novel-type zinc finger domain that is conserved in DNMT3A and DNMT3B but also in ATRX, a member of the SNF2 protein family, The novel domain, called an ADD (ATRX, DNMT3, DNMT3L)-type zinc finger, contains two subparts: a C2C2 and an imperfect PHD zinc finger. Expression of the DNMT3L mRNA was not detectable by Northern blotting; however, RT-PCR amplification revealed that it is expressed at low levels in several tissues including testis, ovary, and thymus. (C) 2000 Academic Press.
引用
收藏
页码:293 / 298
页数:6
相关论文
共 17 条
  • [1] An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains
    Aaltonen, J
    Bjorses, P
    Perheentupa, J
    HorelliKuitunen, N
    Palotie, A
    Peltonen, L
    Lee, YS
    Francis, F
    Hennig, S
    Thiel, C
    Lehrach, H
    Yaspo, ML
    [J]. NATURE GENETICS, 1997, 17 (04) : 399 - 403
  • [2] Blechschmidt K, 1999, GENOME RES, V9, P158
  • [3] Prediction of complete gene structures in human genomic DNA
    Burge, C
    Karlin, S
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1997, 268 (01) : 78 - 94
  • [4] Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping
    Chen, H
    Chrast, R
    Rossier, C
    Morris, MA
    Lalioti, MD
    Antonarakis, SE
    [J]. GENOME RESEARCH, 1996, 6 (08): : 747 - 760
  • [5] Mutations in transcriptional regulator ATRX establish the functional significance of a PHD-like domain
    Gibbons, RJ
    Bachoo, S
    Picketts, DJ
    Aftimos, S
    Asenbauer, B
    Bergoffen, J
    Berry, SA
    Dahl, N
    Fryer, A
    Keppler, K
    Kurosawa, K
    Levin, ML
    Masuno, M
    Neri, G
    Pierpont, ME
    Slaney, SF
    Higgs, DR
    [J]. NATURE GENETICS, 1997, 17 (02) : 146 - 148
  • [6] The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome
    Hansen, RS
    Wijmenga, C
    Luo, P
    Stanek, AM
    Canfield, TK
    Weemaes, CMR
    Gartler, SM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (25) : 14412 - 14417
  • [7] Ishikawa K, 1998, DNA Res, V5, P169, DOI 10.1093/dnares/5.3.169
  • [8] Solution structure of the carboxyl-terminal LIM domain from quail cysteine-rich protein CRP2
    Konrat, R
    Weiskirchen, R
    Krautler, B
    Bister, K
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (18) : 12001 - 12007
  • [9] Kudoh J, 1997, DNA Res, V4, P45, DOI 10.1093/dnares/4.1.45
  • [10] THE DNA (CYTOSINE-5) METHYLTRANSFERASES
    KUMAR, S
    CHENG, XD
    KLIMASAUSKAS, S
    MI, S
    POSFAI, J
    ROBERTS, RJ
    WILSON, GG
    [J]. NUCLEIC ACIDS RESEARCH, 1994, 22 (01) : 1 - 10