AJP - Renal Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Renal Physiol 271: F340-F346, 1996;
0363-6127/96 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Holcomb, T.
Right arrow Articles by Curthoys, N. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Holcomb, T.
Right arrow Articles by Curthoys, N. P.

AJP - Renal Physiology, Vol 271, Issue 2 340-F346, Copyright © 1996 by American Physiological Society


ARTICLES

Promoter elements that mediate the pH response of PCK mRNA in LLC-PK1-F+ cells

T. Holcomb, W. Liu, R. Snyder, R. Shapiro and N. P. Curthoys
Department of Biochemistry and Molecular Biology, Colorado State University, Fort Collins 80523, USA.

The onset of metabolic acidosis causes an increased transcription of the renal phosphoenolpyruvate carboxykinase (PCK) gene. When transgenic mice carrying a bovine growth hormone (bGH) gene driven by the -460 to +73 segment of the PCK promoter were made chronically acidotic, the bGH mRNA was increased twofold after 4 days. Confluent and well-differentiated cultures of LLC-PK1-F+ cells exhibit a 2.5-fold increase in PCK mRNA when transferred to acidic media (pH 6.9, 10 mM HCO3-) for 16 h. Confluent cultures transfected with PCK-490 CAT exhibit an increase (3.5-fold) in chloramphenicol acetyltransferase (CAT) activity when shifted to acidic medium for 48 h. Mutation or deletion of the P2 element causes a four- to fivefold decrease in basal CAT activity but does not affect the pH response. In contrast, mutations of the P3(II) element or the CRE-1 cAMP-response element have little effect on basal activity but cause a 50% decrease in the pH response. Other deletions or mutations have little effect on either activity. Thus changes in the activity or levels of the protein(s) in the renal proximal tubule that binds to the P3(II) and CRE-1 elements may mediate increased transcription of the PCK gene during metabolic acidosis.


This article has been cited by other articles:


Home page
Am. J. Physiol. Heart Circ. Physiol.Home page
H. Christou, N. Bailey, M. S. Kluger, S. A. Mitsialis, and S. Kourembanas
Extracellular acidosis induces heme oxygenase-1 expression in vascular smooth muscle cells
Am J Physiol Heart Circ Physiol, June 1, 2005; 288(6): H2647 - H2652.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Lung Cell. Mol. Physiol.Home page
C. Terminella, K. Tollefson, J. Kroczynski, J. Pelli, and M. Cutaia
Inhibition of apoptosis in pulmonary endothelial cells by altered pH, mitochondrial function, and ATP supply
Am J Physiol Lung Cell Mol Physiol, December 1, 2002; 283(6): L1291 - L1302.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
E. Feifel, P. Obexer, M. Andratsch, S. Euler, L. Taylor, A. Tang, Y. Wei, H. Schramek, N. P. Curthoys, and G. Gstraunthaler
p38 MAPK mediates acid-induced transcription of PEPCK in LLC-PK1-FBPase+ cells
Am J Physiol Renal Physiol, October 1, 2002; 283(4): F678 - F688.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
N. P. Curthoys and G. Gstraunthaler
Mechanism of increased renal gene expression during metabolic acidosis
Am J Physiol Renal Physiol, September 1, 2001; 281(3): F381 - F390.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Cell Physiol.Home page
X. Wang, J. M. Chinsky, P. A. Costeas, and S. R. Price
Acidification and glucocorticoids independently regulate branched-chain {alpha}-ketoacid dehydrogenase subunit genes
Am J Physiol Cell Physiol, May 1, 2001; 280(5): C1176 - C1183.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
O. F. Laterza, L. Taylor, S. Unnithan, L. Nguyen, and N. P. Curthoys
Mapping and functional analysis of an instability element in phosphoenolpyruvate carboxykinase mRNA
Am J Physiol Renal Physiol, November 1, 2000; 279(5): F866 - F873.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
G. Gstraunthaler, T. Holcomb, E. Feifel, W. Liu, N. Spitaler, and N. P. Curthoys
Differential expression and acid-base regulation of glutaminase mRNAs in gluconeogenic LLC-PK1-FBPase+ cells
Am J Physiol Renal Physiol, February 1, 2000; 278(2): F227 - F237.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
W. Liu, E. Feifel, T. Holcomb, X. Liu, N. Spitaler, G. Gstraunthaler, and N. P. Curthoys
PMA and staurosporine affect expression of the PCK gene in LLC-PK1-F+ cells
Am J Physiol Renal Physiol, September 1, 1998; 275(3): F361 - F369.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Renal Physiol.Home page
B. M. Christensen, D. Marples, U. B. Jensen, J. Frokiaer, D. Sheikh-Hamad, M. Knepper, and S. Nielsen
Acute effects of vasopressin V2-receptor antagonist on kidney AQP2 expression and subcellular distribution
Am J Physiol Renal Physiol, August 1, 1998; 275(2): F285 - F297.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
O. F. Laterza, W. R. Hansen, L. Taylor, and N. P. Curthoys
Identification of an mRNA-binding Protein and the Specific Elements That May Mediate the pH-responsive Induction of Renal Glutaminase mRNA
J. Biol. Chem., September 5, 1997; 272(36): 22481 - 22488.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online