Structural and functional characterization of the promoter region of the mouse c-Ki-ras gene

1987 ◽  
Vol 7 (7) ◽  
pp. 2592-2596
Author(s):  
E K Hoffman ◽  
S P Trusko ◽  
N Freeman ◽  
D L George

We isolated and characterized the 5' region of the mouse c-Ki-ras gene, including a 5' untranslated exon (exon 0). These studies used genetic material from Y1 mouse adrenocortical tumor cells in which the c-Ki-ras gene is amplified and overexpressed. Our data demonstrate that transcription initiates at multiple sites, predicting size heterogeneity at the 5' ends of the c-Ki-ras mRNAs. Using transient expression assays, we identified a genomic fragment within the 5' region which exhibits bidirectional promoter activity.

1987 ◽  
Vol 7 (7) ◽  
pp. 2592-2596 ◽  
Author(s):  
E K Hoffman ◽  
S P Trusko ◽  
N Freeman ◽  
D L George

We isolated and characterized the 5' region of the mouse c-Ki-ras gene, including a 5' untranslated exon (exon 0). These studies used genetic material from Y1 mouse adrenocortical tumor cells in which the c-Ki-ras gene is amplified and overexpressed. Our data demonstrate that transcription initiates at multiple sites, predicting size heterogeneity at the 5' ends of the c-Ki-ras mRNAs. Using transient expression assays, we identified a genomic fragment within the 5' region which exhibits bidirectional promoter activity.


PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e11508
Author(s):  
Yubing Yong ◽  
Yue Zhang ◽  
Yingmin Lyu

Background. We have previously performed an analysis of the cold-responsive transcriptome in the mature leaves of tiger lily (Lilium lancifolium) by gene co-expression network identification. The results has revealed that a ZFHD gene, notated as encoding zinc finger homeodomain protein, may play an essential regulating role in tiger lily response to cold stress. Methods. A further investigation of the ZFHD gene (termed as LlZFHD4) responding to osmotic stresses, including cold, salt, water stresses, and abscisic acid (ABA) was performed in this study. Based on the transcriptome sequences, the coding region and 5′ promoter region of LlZFHD4 were cloned from mature tiger lily leaves. Stress response analysis was performed under continuous 4 °C, NaCl, PEG, and ABA treatments. Functional characterization of LlZFHD4 was conducted in transgenic Arabidopsis, tobacco, and yeast. Results. LlZFHD4 encodes a nuclear-localized protein consisting of 180 amino acids. The N-terminal region of LlZFHD4 has transcriptional activation activity in yeast. The 4 °C, NaCl, PEG, and ABA treatments induced the expression of LlZFHD4. Several stress- or hormone-responsive cis-acting regulatory elements (T-Box, BoxI. and ARF) and binding sites of transcription factors (MYC, DRE and W-box) were found in the core promoter region (789 bp) of LlZFHD4. Also, the GUS gene driven by LlZFHD4 promoter was up-regulated by cold, NaCl, water stresses, and ABA in Arabidopsis. Overexpression of LlZFHD4 improved cold and drought tolerance in transgenic Arabidopsis; higher survival rate and better osmotic adjustment capacity were observed in LlZFHD4 transgenic plants compared to wild type (WT) plants under 4 °C and PEG conditions. However, LlZFHD4 transgenic plants were less tolerant to salinity and more hypersensitive to ABA compared to WT plants. The transcript levels of stress- and ABA-responsive genes were much more up-regulated in LlZFHD4 transgenic Arabidopsis than WT. These results indicate LlZFHD4 is involved in ABA signaling pathway and plays a crucial role in regulating the response of tiger lily to cold, salt and water stresses.


2014 ◽  
Vol 99 (5) ◽  
pp. E931-E935 ◽  
Author(s):  
Karen Mei Ling Tan ◽  
Shu Qin Delicia Ooi ◽  
Siong Gim Ong ◽  
Charmaine Shuyi Kwan ◽  
Raymond Ming En Chan ◽  
...  

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Ashutosh Dash ◽  
Vartika Gurdaswani ◽  
Jacinta S. D’Souza ◽  
Siddhesh B. Ghag

2000 ◽  
Vol 20 (5) ◽  
pp. 1335-1339 ◽  
Author(s):  
Ferdinand M. van ′t Hooft ◽  
Björn Lundahl ◽  
Francesca Ragogna ◽  
Fredrik Karpe ◽  
Gunilla Olivecrona ◽  
...  

Hepatology ◽  
1997 ◽  
Vol 26 (4) ◽  
pp. 991-997 ◽  
Author(s):  
G Kullak-Ublick ◽  
U Beuers ◽  
C Fahney ◽  
B Hagenbuch ◽  
P J Meier ◽  
...  

2004 ◽  
Vol 67 (12) ◽  
pp. 2231-2238 ◽  
Author(s):  
Christelle Cauffiez ◽  
Florian Klinzig ◽  
Emmanuel Rat ◽  
Gilles Tournel ◽  
Delphine Allorge ◽  
...  

2010 ◽  
Vol 1 (1) ◽  
pp. 213-213
Author(s):  
T Alam ◽  
B Bahar ◽  
S Waters ◽  
M McGee ◽  
T Sweeney

2009 ◽  
Vol 37 (4) ◽  
pp. 1699-1705 ◽  
Author(s):  
Mingjun Liu ◽  
Zhenhua Sun ◽  
Aidong Zhou ◽  
Hong Li ◽  
Liping Yang ◽  
...  

2003 ◽  
Vol 373 (3) ◽  
pp. 835-843 ◽  
Author(s):  
Mònica TORRAS-LLORT ◽  
Fernando AZORÍN

In this paper, the human phosphodiesterase 7A1 (hPDE7A1) promoter region was identified and functionally characterized. Transient transfection experiments indicated that a 2.9 kb fragment of the hPDE7A1 5′-flanking region, to position −2907, has strong promoter activity in Jurkat T-cells. Deletion analysis showed that the proximal region, up to position −988, contains major cis-regulatory elements of the hPDE7A1 promoter. This minimal promoter region contains a regulatory CpG island which is essential for promoter activity. The CpG island contains three potential cAMP-response-element-binding protein (CREB)-binding sites that, as judged by in vivo dimethyl sulphate (DMS) footprinting, are occupied in Jurkat T-cells. Moreover, over-expression of CREB results in increased promoter activity, but, on the other hand, promoter activity decreases when a dominant-negative form of CREB (KCREB) is over-expressed. In vivo DMS footprinting strongly indicates that other transcription factors, such Ets-2, nuclear factor of activated T-cells 1 (NFAT-1) and nuclear factor κB (NF-κB), might also contribute to the regulation of hPDE7A1 promoter. Finally, hPDE7A1 promoter was found to be induced by treatment with PMA, but not by treatment with dibutyryl cAMP or forskolin. These results provide insights into the factors and mechanisms that regulate expression of the hPDE7A gene.


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