help button home button Endocrine Society Endocrinology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
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
Right arrow Request Copyright Permission
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Day, R.
Right arrow Articles by Akil, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Day, R.
Right arrow Articles by Akil, H.

Endocrinology, Vol 124, 2392-2405, Copyright © 1989 by Endocrine Society


ARTICLES

The posttranslational processing of prodynorphin in the rat anterior pituitary

R Day and H Akil
University of Michigan, Mental Health Research Institute, Ann Arbor 48109.

The posttranslational processing of prodynorphin (Pro-Dyn) is not well understood. The rat anterior pituitary is an interesting tissue which merits examination to address this issue since it is known that Dyn immunoreactivity is stored as high mol wt (HMW) intermediates and not as free products such as dynorphin-A-(1-17) (Dyn-A17) or dynorphin-B-(1- 13) (Dyn-B). The aim of our study is to characterize the Pro-Dyn products in the rat anterior pituitary quantitatively as well as qualitatively by keeping a close account of each of the possible domains that are known to compose the protein structure. This was achieved by a convergence of tools: designing RIA with antibodies to each of these domains, including antibodies to Dyn-A17, Dyn-B, alpha- neo-endorphin, bridge peptide, and Pro-Dyn carboxyl-terminal peptide (C- peptide), and using these antisera with gel filtration chromatography, reverse phase HPLC, immunoaffinity, and immunoprecipitation techniques. Our data indicate the presence of at least six distinct molecules which are classified as HMW intermediates (greater than 3.5K). By gel filtration chromatography they have apparent mol wt of 16,000, 10,000, 8,000, 6,000, 4,000, and 3,500, respectively. Each of these structures is characterized by multiple immunoreactivities to account for the observed mass. Based on the relative content of each structure we present a scheme for the posttranslational processing pathway of Pro- Dyn in the rat anterior pituitary. We also analyze other tissues, spinal cord and hypothalamus, for their content of Pro-Dyn HMW intermediates. Our results indicate that these tissues store Pro-Dyn HMW molecules of similar sizes and immunoreactive properties, suggesting that Pro-Dyn may be processed in a similar manner, at least in the initial phases, across tissues.


This article has been cited by other articles:


Home page
FASEB J.Home page
T. Yakovleva, I. Bazov, G. Cebers, Z. Marinova, Y. Hara, A. Ahmed, M. Vlaskovska, B. Johansson, U. Hochgeschwender, I. N. Singh, et al.
Prodynorphin storage and processing in axon terminals and dendrites
FASEB J, October 1, 2006; 20(12): 2124 - 2126.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
Z. Marinova, V. Vukojevic, S. Surcheva, T. Yakovleva, G. Cebers, N. Pasikova, I. Usynin, L. Hugonin, W. Fang, M. Hallberg, et al.
Translocation of Dynorphin Neuropeptides across the Plasma Membrane: A PUTATIVE MECHANISM OF SIGNAL TRANSMISSION
J. Biol. Chem., July 15, 2005; 280(28): 26360 - 26370.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
R. Day, C. Lazure, A. Basak, A. Boudreault, P. Limperis, W. Dong, and I. Lindberg
Prodynorphin Processing by Proprotein Convertase 2. CLEAVAGE AT SINGLE BASIC RESIDUES AND ENHANCED PROCESSING IN THE PRESENCE OF CARBOXYPEPTIDASE ACTIVITY
J. Biol. Chem., January 9, 1998; 273(2): 829 - 836.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
I. De Bie, D. Savaria, A. J. M. Roebroek, R. Day, C. Lazure, W. J. M. Van de Ven, and N. G. Seidah
Processing Specificity and Biosynthesis of the Drosophila melanogaster Convertases dfurin1, dfurin1-CRR, dfurin1-X, and dfurin2
J. Biol. Chem., January 20, 1995; 270(3): 1020 - 1028.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Endocrinology Endocrine Reviews J. Clin. End. & Metab.
Molecular Endocrinology Recent Prog. Horm. Res. All Endocrine Journals
Copyright © 1989 by The Endocrine Society