Transcriptional Activities of a Winged Bean Kunitz Chymotrypsin Inhibitor Gene Promoter in Stable and Transient Expression Systems

1994 ◽  
Vol 58 (11) ◽  
pp. 2104-2106 ◽  
Author(s):  
Yoichi Sakata ◽  
Hisayo Fukushima ◽  
Yoshiki Habu ◽  
Shigeki Furuya ◽  
Satoshi Naito ◽  
...  
1999 ◽  
Vol 40 (1) ◽  
pp. 109-113 ◽  
Author(s):  
M. Minami ◽  
G. Morisawa ◽  
M. Hayashi ◽  
Y. Sakata ◽  
Y. Habu ◽  
...  

1993 ◽  
Vol 23 (6) ◽  
pp. 1139-1150 ◽  
Author(s):  
Yoshiki Habu ◽  
Yoichi Sakata ◽  
Kazuhiro Fukasawa ◽  
Takeshi Ohno

2010 ◽  
Vol 8 (5) ◽  
pp. 638-654 ◽  
Author(s):  
Gregory P. Pogue ◽  
Fakhrieh Vojdani ◽  
Kenneth E. Palmer ◽  
Ernie Hiatt ◽  
Steve Hume ◽  
...  

2007 ◽  
Vol 138 (2) ◽  
pp. 231-244 ◽  
Author(s):  
Mathieu Garand ◽  
Nazareth Bastajian ◽  
Michael E. Nesheim ◽  
Michael B. Boffa ◽  
Marlys L. Koschinsky

Blood ◽  
1994 ◽  
Vol 84 (11) ◽  
pp. 3929-3935 ◽  
Author(s):  
S Safaya ◽  
A Ibrahim ◽  
RF Rieder

Butyric acid increases fetal hemoglobin synthesis in adult animals and in erythroid cells in culture and induces the gamma-globin gene promoter in transient expression experiments in K562 cells (McDonagh KT, Nienhuis AW, Blood 78:255a, 1992 [abstr, suppl 1]). We compared the effect of butyrate and other short-chain carboxylic acids in transient expression studies with K562 cells using an expression plasmid bearing a luciferase reporter gene driven by the normal human A gamma-globin gene promoter. Butyrate (4 carbons) increased the activity of the human A gamma-globin gene promoter up to 123 times. Marked augmentation of the normal gamma-promoter activity was also noted with 5-carbon valeric acid (up to 394 times) and 3-carbon propionic acid (up to 129 times). The branched isobutyric acid as well as phenylacetate showed less ability to increase promoter activity. Addition of the tandemly repeated AP-1/NF-E2 (AP) enhancer sequences from hypersensitive site 2 (HS2) of the locus control region (LCR) increased gamma-promoter activity up to 24 times. Addition of a nearby 16-bp conserved motif (CM) in HS2 (Safaya S, Rieder RF, Blood 78:146a, 1992 [abstr, suppl 1]) to the AP-containing plasmid construct further increased gamma-promoter activity. In the presence of butyrate, the plasmid bearing both the AP and CM sequences showed gene expression up to 477 times greater than that of the basal gamma-promoter-driven luciferase plasmid in the absence of inducer. A plasmid bearing the herpes simplex thymidine kinase promoter was also tested and gene expression was markedly increased by the same organic acids. MEL cells responded to butyrate, valerate, and propionate with induction of hemoglobin synthesis. Responses to isobutyrate and 6-carbon caproate required higher concentrations of the compounds. Thus, other short-chain organic acids as well as butyrate increase gamma-promoter activity in the transient expression system, and this activity can be further augmented by incorporating LCR elements into the expression vector. Nonglobin promoters also respond to the same carboxylic acids.


Blood ◽  
1996 ◽  
Vol 87 (12) ◽  
pp. 5074-5084 ◽  
Author(s):  
S Okinaga ◽  
K Takahashi ◽  
K Takeda ◽  
M Yoshizawa ◽  
H Fujita ◽  
...  

Heme oxygenase-1 is an essential enzyme in heme catabolism, and its human gene promoter contains a putative heat shock element (HHO-HSE). This study was designed to analyze the regulation of human heme oxygenase-1 gene expression under thermal stress. The amounts of heme oxygenase-1 protein were not increased by heat shock (incubation at 42 degrees C) in human alveolar macrophages and in a human erythroblastic cell line, YN-1–0-A, whereas heat shock protein 70 (HSP70) was noticeably induced. However, heat shock factor does bind in vitro to HHO-HSE and the synthetic HHO-HSE by itself is sufficient to confer the increase in the transient expression of a reporter gene upon heat shock. The deletion of the sequence, located downstream from HHO-HSE, resulted in the activation of a reporter gene by heat shock. These results suggest that HHO-HSE is potentially functional but is repressed in vivo. Interestingly, heat shock abolished the remarkable increase in the levels of heme oxygenase-1 mRNA in YN-1–0-A cells treated with hemin or cadmium, in which HSP70 mRNA was noticeably induced. Furthermore, transient expression assays showed that heat shock inhibits the cadmium-mediated activation of the heme oxygenase-1 promoter, whereas the HSP70 gene promoter was activated upon heat shock. Such regulation of heme oxygenase-1 under thermal stress may be of physiologic significance in erythroid cells.


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