help button home button Endocrine Society Molecular Endocrinology ENDO 08 Sessions Library
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Molecular Endocrinology Vol. 6, No. 6 969-977
doi:10.1210/me.6.6.969
Copyright © 1992 by the Endocrine Society.
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
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 Pao, C. I.
Right arrow Articles by Phillips, L. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Pao, C. I.
Right arrow Articles by Phillips, L. S.

Molecular Endocrinology, Vol 6, 969-977, Copyright © 1992 by Endocrine Society


ARTICLES

Expression of hepatic insulin-like growth factor-I and insulin-like growth factor-binding protein-1 genes is transcriptionally regulated in streptozotocin-diabetic rats

CI Pao, PK Farmer, S Begovic, S Goldstein, GJ Wu and LS Phillips
Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30303.

Insulin-like growth factor-I (IGF-I) and IGF-binding protein-1 (BP-1) are critical cell regulators, with regulation and action in endocrine, paracrine, and autocrine modes. Although IGF-I and BP-1 are thought to be modulated mainly at the level of synthesis, underlying molecular mechanisms are poorly understood. To examine regulation by insulin, we used run-on assays to measure IGF-I and BP-1 gene transcription rates in nuclei isolated from the livers of normal and diabetic rats. Streptozotocin (STZ)-treated rats exhibited 20-25% weight loss, a 2.5- to 3-fold increase in serum glucose, and a 50-60% fall in circulating IGF-I levels (all P less than 0.001). Diabetic animals also had a 45% reduction in hepatic IGF-I mRNA and over 400% increases in BP-1 mRNA (both P less than 0.005); all parameters were restored toward normal after treatment with insulin. Metabolically responsive IGF-I gene transcription was evaluated effectively with a 3.2-kilobase BglII/EcoRI genomic probe located down-stream from all initiation sites in exon 1, while BP-1 gene transcription was studied with a cDNA probe. Animals treated with 144 mg/kg STZ exhibited 50-97% decreases in IGF-I gene transcription (P less than 0.05), while insulin treatment raised IGF-I gene transcription to control levels (P less than 0.02). IGF-I gene transcription appeared to be more sensitive to metabolic status than IGF-I mRNA levels, resulting in a modest correlation between transcription rates and mRNA levels (r = 0.68; P less than 0.001). In contrast, changes in BP-1 mRNA and gene transcription appeared to be exquisitely sensitive to metabolic status.(ABSTRACT TRUNCATED AT 250 WORDS)


This article has been cited by other articles:


Home page
EndocrinologyHome page
P. Froment, C. Staub, S. Hembert, C. Pisselet, M. Magistrini, B. Delaleu, D. Seurin, J. E. Levine, L. Johnson, M. Binoux, et al.
Reproductive Abnormalities in Human Insulin-Like Growth Factor-Binding Protein-1 Transgenic Male Mice
Endocrinology, April 1, 2004; 145(4): 2080 - 2091.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
R. E. Schmidt, D. A. Dorsey, L. N. Beaudet, and R. G. Peterson
Analysis of the Zucker Diabetic Fatty (ZDF) Type 2 Diabetic Rat Model Suggests a Neurotrophic Role for Insulin/IGF-I in Diabetic Autonomic Neuropathy
Am. J. Pathol., July 1, 2003; 163(1): 21 - 28.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
P. Froment, D. Seurin, S. Hembert, J. E. Levine, C. Pisselet, D. Monniaux, M. Binoux, and P. Monget
Reproductive Abnormalities in Human IGF Binding Protein-1 Transgenic Female Mice
Endocrinology, May 1, 2002; 143(5): 1801 - 1808.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
E. N. Kaytor, J. L. Zhu, C.-I Pao, and L. S. Phillips
Physiological Concentrations of Insulin Promote Binding of Nuclear Proteins to the Insulin-Like Growth Factor I Gene
Endocrinology, March 1, 2001; 142(3): 1041 - 1049.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
J.-L. Zhu, C.-I Pao, E. Hunter Jr., K.-w. M. Lin, G.-j. Wu, and L. S. Phillips
Identification of Core Sequences Involved in Metabolism-Dependent Nuclear Protein Binding to the Rat Insulin-Like Growth Factor I Gene
Endocrinology, October 1, 1999; 140(10): 4761 - 4771.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
G. Schweizer-Groyer, N. Jibard, E. Neau, D. Fortin, F. Cadepond, E.-E. Baulieu, and A. Groyer
The Glucocorticoid Response Element II Is Functionally Homologous in Rat and Human Insulin-like Growth Factor-binding Protein-1 Promoters
J. Biol. Chem., April 23, 1999; 274(17): 11679 - 11686.
[Abstract] [Full Text] [PDF]


Home page
Mol. Endocrinol.Home page
D.-S. Suh and M. M. Rechler
Hepatocyte Nuclear Factor 1 and the Glucocorticoid Receptor Synergistically Activate Transcription of the Rat Insulin-like Growth Factor Binding Protein-1 Gene
Mol. Endocrinol., November 1, 1997; 11(12): 1822 - 1831.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
C.-I Pao, J.-l. Zhu, D. G. Robertson, K.-w. M. Lin, P. K. Farmer, S. Begovic, G.-j. Wu, and L. S. Phillips
Transcriptional Regulation of the Rat Insulin-like Growth Factor-I Gene Involves Metabolism-dependent Binding of Nuclear Proteins to a Downstream Region
J. Biol. Chem., October 20, 1995; 270(42): 24917 - 24923.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
E. N. Kaytor, J. L. Zhu, C.-I Pao, and L. S. Phillips
Insulin-responsive Nuclear Proteins Facilitate Sp1 Interactions with the Insulin-like Growth Factor-I Gene
J. Biol. Chem., September 28, 2001; 276(40): 36896 - 36901.
[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 © 1992 by The Endocrine Society