TY - JOUR
T1 - TGFβ-inducible early gene (TIEG) also codes for early growth response a (EGRα)
T2 - Evidence of multiple transcripts from alternate promoters
AU - Fautsch, Michael P.
AU - Vrabel, Anne
AU - Subramaniam, Malayannan
AU - Hefferen, Theresa E.
AU - Spelsberg, Thomas C.
AU - Wieben, Eric D.
N1 - Funding Information:
We thank Dr. Kim Tau for her technical assistance at the start of this project and Debbie Pearson for help in preparing the manuscript. This work is supported by NIH Grant AR-43627 and the Mayo Foundation.
PY - 1998/8/1
Y1 - 1998/8/1
N2 - TGFβ-inducible early gene (TIEG) and early growth response α (EGRα) are putative transcription factors based on homology to known zinc finger proteins SP1, EGR1, BTEB, and Wilm tumor. Here we report that TIEG and EGRα are expressed from alternative promoters of the same gene. The TIEG/EGRα gene spans 8 kb and contains five exons. Use of alternative first exons results in TIEG having 12 unique amino acids on its N-terminus. Computer analysis of the 5' upstream regions of either TIEG (exon 1a) or EGRα (exon 1b) does not identify a TATA box or initiator sequence but shows consensus sequence similarities to binding sites for several transcription factors including SP1, JunB, and aromatic hydrocarbon/receptor-ligand complexes. Analysis of constructs containing 5'-flanking regions show that both the TIEG and the EGRα promoters have significant activity in human fetal osteoblast cells. Northern analysis of mRNA from various human tissues and several cell lines reveals that TIEG is the predominant transcript produced and regulated by growth factors from the TIEG/EGRα gene.
AB - TGFβ-inducible early gene (TIEG) and early growth response α (EGRα) are putative transcription factors based on homology to known zinc finger proteins SP1, EGR1, BTEB, and Wilm tumor. Here we report that TIEG and EGRα are expressed from alternative promoters of the same gene. The TIEG/EGRα gene spans 8 kb and contains five exons. Use of alternative first exons results in TIEG having 12 unique amino acids on its N-terminus. Computer analysis of the 5' upstream regions of either TIEG (exon 1a) or EGRα (exon 1b) does not identify a TATA box or initiator sequence but shows consensus sequence similarities to binding sites for several transcription factors including SP1, JunB, and aromatic hydrocarbon/receptor-ligand complexes. Analysis of constructs containing 5'-flanking regions show that both the TIEG and the EGRα promoters have significant activity in human fetal osteoblast cells. Northern analysis of mRNA from various human tissues and several cell lines reveals that TIEG is the predominant transcript produced and regulated by growth factors from the TIEG/EGRα gene.
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U2 - 10.1006/geno.1998.5388
DO - 10.1006/geno.1998.5388
M3 - Article
C2 - 9721211
AN - SCOPUS:0032129209
SN - 0888-7543
VL - 51
SP - 408
EP - 416
JO - Genomics
JF - Genomics
IS - 3
ER -