Structural diversity and functional implications of the eukaryotic TDP gene family

被引:250
作者
Wang, HY
Wang, IF
Bose, J
Shen, CKJ [1 ]
机构
[1] Acad Sinica, Inst Mol Biol, Taipei 115, Taiwan
[2] Natl Taiwan Univ, Inst Mol Med, Sch Med, Taipei 106, Taiwan
关键词
TDP family; evolution; Exon skipping; alternative splicing;
D O I
10.1016/S0888-7543(03)00214-3
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
TDP-43 is an RNA-binding protein that functions in mammalian cells in transcriptional repression and exon skipping. The gene encoding TDP-43 (HGMW-approved gene symbol TARDBP) is conserved in human, mouse, Drosophila melanogaster, and Caenorhabditis elegans. Sequence comparison of the coding regions of the TDP genes among the four taxa reveals an extraordinarily low rate of sequence divergence, suggesting that the TDP genes carry out essential functions in these organisms. With DNA transfection assay, we have established the importance of the glycine-rich domain for the exon-skipping activity of TDP-43. Both human and mouse TDP genes belong to a gene family that also consists of a number of processed pseudogenes. Interestingly, combined database analysis and cDNA cloning have demonstrated that the primary transcript of the mammalian TDP genes undergoes alternative splicing to generate I I mRNAs, including the one encoding TDP-43. Eight of the I I splicing events involved the use of four each of the 5'-donor and 3'-acceptor sites, all of which reside within the last exon of the TDP-43 mRNA. The existence of multispliced isoforms of TDP-encoded proteins provides further support for the functional complexity of the eukaryotic TDP genes. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:130 / 139
页数:10
相关论文
共 31 条
  • [1] Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9
    Buratti, E
    Baralle, FE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (39) : 36337 - 36343
  • [2] Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping
    Buratti, E
    Dörk, T
    Zuccato, E
    Pagani, F
    Romano, M
    Baralle, FE
    [J]. EMBO JOURNAL, 2001, 20 (07) : 1774 - 1784
  • [3] Evolutionary fates and origins of U12-type introns
    Burge, CB
    Padgett, RA
    Sharp, PA
    [J]. MOLECULAR CELL, 1998, 2 (06) : 773 - 785
  • [4] Analysis of canonical and non-canonical splice sites in mammalian genomes
    Burset, M
    Seledtsov, IA
    Solovyev, VV
    [J]. NUCLEIC ACIDS RESEARCH, 2000, 28 (21) : 4364 - 4375
  • [5] hnRNP A1 selectively interacts through its Gly-rich domain with different RNA-binding proteins
    Cartegni, L
    Maconi, M
    Morandi, E
    Cobianchi, F
    Riva, S
    Biamonti, G
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1996, 259 (03) : 337 - 348
  • [6] HNRNP PROTEINS AND THE BIOGENESIS OF MESSENGER-RNA
    DREYFUSS, G
    MATUNIS, MJ
    PINOLROMA, S
    BURD, CG
    [J]. ANNUAL REVIEW OF BIOCHEMISTRY, 1993, 62 : 289 - 321
  • [7] Functional architecture in the cell nucleus
    Dundr, M
    Misteli, T
    [J]. BIOCHEMICAL JOURNAL, 2001, 356 (02) : 297 - 310
  • [8] An RNA recognition motif (RRM) is required for the localization of PTB-associated splicing factor (PSF) to subnuclear speckles
    Dye, BT
    Patton, JG
    [J]. EXPERIMENTAL CELL RESEARCH, 2001, 263 (01) : 131 - 144
  • [9] Testing the neutral theory of molecular evolution with genomic data from Drosophila
    Fay, JC
    Wyckoff, GJ
    Wu, CI
    [J]. NATURE, 2002, 415 (6875) : 1024 - 1026
  • [10] ON THE ANTIQUITY OF INTRONS
    GILBERT, W
    MARCHIONNI, M
    MCKNIGHT, G
    [J]. CELL, 1986, 46 (02) : 151 - 154