scholarly journals Regulation of the gene for human dipeptidyl peptidase IV by hepatocyte nuclear factor 1α

1999 ◽  
Vol 338 (1) ◽  
pp. 91-97 ◽  
Author(s):  
Roger H. ERICKSON ◽  
James R. GUM ◽  
Craig D. LOTTERMAN ◽  
James W. HICKS ◽  
Roy S. LAI ◽  
...  

Hepatocyte nuclear factor 1 was identified as the transcription factor binding to a 20 bp (-150 to -131) region of the gene for human dipeptidyl peptidase IV, which has been shown to be important for the expression of dipeptidyl peptidase IV in the human intestinal and hepatic epithelial cell lines Caco-2 and HepG2. Functional analysis of the hepatocyte nuclear factor 1 site was performed with two minimal dipeptidyl peptidase IV promoter constructs (-250 to -41, and -150 to -41) with and without a 3 bp mutation in the hepatocyte nuclear factor 1 sequence, and used in transient transfection experiments with Caco-2 cells. The results show that the mutated constructs were able to drive transcription at only 5–10% of the activity of the non-mutated controls. Co-transfection of 3T3 cells with hepatocyte nuclear factor 1 (α or β) and dipeptidyl peptidase IV promoter constructs (-250 to -41 or -150 to -41) resulted in a 2.5–6-fold increase in transcription over controls with hepatocyte nuclear factor 1α but not with hepatocyte nuclear factor 1β. The results of this study show that hepatocyte nuclear factor 1 binds to the -150 to -131 region of the human dipeptidyl peptidase IV promoter and is necessary for transcriptional activation of the gene for dipeptidyl peptidase IV.

1998 ◽  
Vol 114 ◽  
pp. A878
Author(s):  
Roger H. Erickson ◽  
James R. Gum ◽  
Craig D. Lotterman ◽  
James W. Hicks ◽  
Young S. Kim

1999 ◽  
Vol 338 (1) ◽  
pp. 91 ◽  
Author(s):  
Roger H. ERICKSON ◽  
James R. GUM ◽  
Craig D. LOTTERMAN ◽  
James W. HICKS ◽  
Roy S. LAI ◽  
...  

1993 ◽  
Vol 13 (4) ◽  
pp. 2401-2410 ◽  
Author(s):  
D A Jackson ◽  
K E Rowader ◽  
K Stevens ◽  
C Jiang ◽  
P Milos ◽  
...  

The liver-specific enhancer of the serum albumin gene contains an essential segment, designated eH, which binds the hepatocyte nuclear factor 3 alpha (HNF3 alpha) and ubiquitous nuclear factor 1/CCAAT transcription factor (NF1/CTF) proteins in tight apposition. We previously showed that activation of transcription by the eH site was correlated with an increase in intracellular HNF3 alpha levels during the in vitro differentiation of the hepatic cell line H2.35. We now show that transfection of an HNF3 alpha cDNA expression vector into dedifferentiated H2.35 cells is sufficient to induce transcription from the eH site. Mutational analysis of the enhancer demonstrates that NF1/CTF cooperates with HNF3 alpha to induce enhancer activity. However, when the eH site is removed from the context of the enhancer, NF1/CTF can inhibit transcriptional activation by HNF3 alpha. We conclude that the ternary complex of HNF3 alpha, NF1/CTF, and the eH site forms a novel, composite regulatory element that is sensitive to the local DNA sequence environment and suggest that the transcriptional stimulatory activity of NF1/CTF depends on its higher-order interactions with other proteins during hepatocyte differentiation.


1993 ◽  
Vol 13 (4) ◽  
pp. 2401-2410
Author(s):  
D A Jackson ◽  
K E Rowader ◽  
K Stevens ◽  
C Jiang ◽  
P Milos ◽  
...  

The liver-specific enhancer of the serum albumin gene contains an essential segment, designated eH, which binds the hepatocyte nuclear factor 3 alpha (HNF3 alpha) and ubiquitous nuclear factor 1/CCAAT transcription factor (NF1/CTF) proteins in tight apposition. We previously showed that activation of transcription by the eH site was correlated with an increase in intracellular HNF3 alpha levels during the in vitro differentiation of the hepatic cell line H2.35. We now show that transfection of an HNF3 alpha cDNA expression vector into dedifferentiated H2.35 cells is sufficient to induce transcription from the eH site. Mutational analysis of the enhancer demonstrates that NF1/CTF cooperates with HNF3 alpha to induce enhancer activity. However, when the eH site is removed from the context of the enhancer, NF1/CTF can inhibit transcriptional activation by HNF3 alpha. We conclude that the ternary complex of HNF3 alpha, NF1/CTF, and the eH site forms a novel, composite regulatory element that is sensitive to the local DNA sequence environment and suggest that the transcriptional stimulatory activity of NF1/CTF depends on its higher-order interactions with other proteins during hepatocyte differentiation.


2000 ◽  
Vol 275 (17) ◽  
pp. 12515-12520 ◽  
Author(s):  
Evi Soutoglou ◽  
George Papafotiou ◽  
Nitsa Katrakili ◽  
Iannis Talianidis

2005 ◽  
Vol 280 (48) ◽  
pp. 39827-39834 ◽  
Author(s):  
Shin-ichi Satoh ◽  
Takashi Noaki ◽  
Tatsuya Ishigure ◽  
Shigehiro Osada ◽  
Masayoshi Imagawa ◽  
...  

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