|
|
||||||||
1 Section of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, USA
2 Research and Development Division, Jesse Brown Veterans Administration Medical Center, Chicago, Illinois, USA
(Requests for offprints should be addressed to R M Luque who is now at Research and Development Division, Jesse Brown VA Medical Center, M.P 151, West Side, Suite #6215, 820 South Damen Avenue, Chicago, Illinois 60612, USA; Email: luque{at}uic.edu)
The mouse ghrelin gene contains 5 exons (Ex), with Ex2Ex5 encoding a 117 amino acid preproprotein that is processed to yield a 28 amino acid mature peptide. The current study examined if pituitary (PIT) and hypothalamus (HPT) ghrelin expression is up-regulated in response to fasting and down-regulated in obesity, as previously reported in the stomach. In the process of establishing a quantitative real-time RT-PCR system to accurately assess the changes in PIT and HPT ghrelin mRNA levels, we observed that primer sets located in Ex2 and Ex3 amplified a ghrelin transcript that contained the entire intron 2 (In2). Size and sequence analysis of RT-PCR products using multiple primer sets located throughout the ghrelin gene suggested that the In2-ghrelin variant contains Ex2 and Ex3, but lacks Ex1, Ex4, and Ex5. In2-ghrelin variant mRNA was not detected in stomach extracts, while expression levels were 10- and 50-fold greater than that of the native ghrelin transcript in the PIT and HPT respectively. In2-ghrelin variant mRNA levels increased in the PIT after 24 h fasting and decreased in the HPT and PIT of diet-induced obese mice. These changes may be due to the changes in circulating insulin or IGF-I, since both decreased In2-ghrelin variant expression in a mouse HPT cell line (N6) and in primary mouse PIT cell cultures. The fact that In2-ghrelin variant mRNA levels are dependent on energy intake in the PIT and HPT suggests that this transcript may encode a peptide important in coordinating the neuroendocrine response to metabolic stress.
This article has been cited by other articles:
![]() |
P. T. Pfluger, H. Kirchner, S. Gunnel, B. Schrott, D. Perez-Tilve, S. Fu, S. C. Benoit, T. Horvath, H.-G. Joost, K. E. Wortley, et al. Simultaneous deletion of ghrelin and its receptor increases motor activity and energy expenditure Am J Physiol Gastrointest Liver Physiol, March 1, 2008; 294(3): G610 - G618. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. M. Luque, R. D. Kineman, and M. Tena-Sempere Regulation of Hypothalamic Expression of KiSS-1 and GPR54 Genes by Metabolic Factors: Analyses Using Mouse Models and a Cell Line Endocrinology, October 1, 2007; 148(10): 4601 - 4611. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |