TY - JOUR
T1 - Structural diversity and functional implications of the eukaryotic TDP gene family
AU - Wang, Hurng Yi
AU - Wang, I. Fan
AU - Bose, Jayaramakrishnan
AU - Shen, C. K.James
N1 - Funding Information:
We thank W.-T. Tarn and Hung Li for materials and helpful discussions. This research was supported by the Academia Sinica and the National Science Council, Taipei, Taiwan, ROC, and the Macmicro Biotechnology Corp. H.Y. Wang is a recipient of a postdoctoral fellowship from Academia Sinica and also sponsored by the Ministry of National Defense, Taiwan, ROC.
PY - 2004/1
Y1 - 2004/1
N2 - 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 11 mRNAs, including the one encoding TDP-43. Eight of the 11 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.
AB - 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 11 mRNAs, including the one encoding TDP-43. Eight of the 11 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.
KW - Alternative splicing
KW - Evolution
KW - Exon skipping
KW - TDP family
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U2 - 10.1016/S0888-7543(03)00214-3
DO - 10.1016/S0888-7543(03)00214-3
M3 - Article
C2 - 14667816
AN - SCOPUS:0344256486
SN - 0888-7543
VL - 83
SP - 130
EP - 139
JO - Genomics
JF - Genomics
IS - 1
ER -