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Structural diversity and functional implications of the eukaryotic TDP gene family
被引:255
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
来源:
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.
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页码:130 / 139
页数:10
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