Post-transcriptional regulation of insulin-like growth factor binding protein-2 mRNA in diabetic rat liver

IGFBP-1 and IGFBP-2 mRNAs are increased in the livers of streptozotocin-diabetic rats. A corresponding increase is observed in transcription of the IGFBP-1 but not the IGFBP-2 gene, indicating that the increase in steady-state levels of IGFBP-2 mRNA is a post-transcriptional effect. IGFBP-1 and IGFB...

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Published inBiochemical and biophysical research communications Vol. 189; no. 2; pp. 1031 - 1037
Main Authors Ooi, Guck T., Y.-H. Tseng, Lucy, Rechler, Matthew M.
Format Journal Article
LanguageEnglish
Published San Diego, CA Elsevier Inc 15.12.1992
Elsevier
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Abstract IGFBP-1 and IGFBP-2 mRNAs are increased in the livers of streptozotocin-diabetic rats. A corresponding increase is observed in transcription of the IGFBP-1 but not the IGFBP-2 gene, indicating that the increase in steady-state levels of IGFBP-2 mRNA is a post-transcriptional effect. IGFBP-1 and IGFBP-2 mRNAs also differ in the rapidity of their response to insulin treatment: hepatic IGFBP-1 mRNA is normalized within 1 h, IGFBP-2 mRNA decreases more slowly. These differences suggest that IGFBP-2 may provide more chronic adaptation to metabolic change than IGFBP-1.
AbstractList IGFBP-1 and IGFBP-2 mRNAs are increased in the livers of streptozotocin-diabetic rats. A corresponding increase is observed in transcription of the IGFBP-1 but not the IGFBP-2 gene, indicating that the increase in steady-state levels of IGFBP-2 mRNA is a post-transcriptional effect. IGFBP-1 and IGFBP-2 mRNAs also differ in the rapidity of their response to insulin treatment: hepatic IGFBP-1 mRNA is normalized within 1 h, IGFBP-2 mRNA decreases more slowly. These differences suggest that IGFBP-2 may provide more chronic adaptation to metabolic change than IGFBP-1
IGFBP-1 and IGFBP-2 mRNAs are increased in the livers of streptozotocin-diabetic rats. A corresponding increase is observed in transcription of the IGFBP-1 but not the IGFBP-2 gene, indicating that the increase in steady-state levels of IGFBP-2 mRNA is a post-transcriptional effect. IGFBP-1 and IGFBP-2 mRNAs also differ in the rapidity of their response to insulin treatment: hepatic IGFBP-1 mRNA is normalized within 1 h, IGFBP-2 mRNA decreases more slowly. These differences suggest that IGFBP-2 may provide more chronic adaptation to metabolic change than IGFBP-1.
Author Ooi, Guck T.
Y.-H. Tseng, Lucy
Rechler, Matthew M.
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Issue 2
Keywords Endocrinopathy
Rat
Diabetes mellitus
Liver
Rodentia
Insulin like growth factor 2
Insulin
Posttranscriptional modification
Protein hormone
Binding protein
Vertebrata
Chronic
Mammalia
Polypeptide
Kinetics
Growth factor
Language English
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PublicationTitle Biochemical and biophysical research communications
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PublicationYear 1992
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Elsevier
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Snippet IGFBP-1 and IGFBP-2 mRNAs are increased in the livers of streptozotocin-diabetic rats. A corresponding increase is observed in transcription of the IGFBP-1 but...
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SubjectTerms Analytical, structural and metabolic biochemistry
Animals
ARN MENSAJERO
ARN MESSAGER
Binding and carrier proteins
Biological and medical sciences
Blotting, Northern
Carrier Proteins - biosynthesis
Carrier Proteins - genetics
Cell Nucleus - physiology
DIABETE
DIABETES
Diabetes Mellitus, Experimental - metabolism
EXPERIMENTATION
EXPERIMENTOS
FOIE
Fundamental and applied biological sciences. Psychology
GENE
GENES
HIGADO
Insulin - pharmacology
Insulin, Isophane - pharmacology
Insulin-Like Growth Factor Binding Protein 1
Insulin-Like Growth Factor Binding Protein 2
INSULINA
INSULINE
Kinetics
Liver - drug effects
Liver - metabolism
Male
PROTEINAS
PROTEINE
Proteins
RAT
RATA
Rats
Rats, Sprague-Dawley
RNA Processing, Post-Transcriptional
RNA, Messenger - genetics
RNA, Messenger - metabolism
Somatomedins - metabolism
Transcription, Genetic - drug effects
Title Post-transcriptional regulation of insulin-like growth factor binding protein-2 mRNA in diabetic rat liver
URI https://dx.doi.org/10.1016/0006-291X(92)92307-J
https://www.ncbi.nlm.nih.gov/pubmed/1281986
https://search.proquest.com/docview/73398165
Volume 189
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