Genetic analysis of L-ethionine-mediated induction of alpha-fetoprotein in mice

Two genetic loci regulate hepatic alpha-fetoprotein (AFP) mRNA levels in adult mice. The raf locus controls basal levels and the Rif locus determines the degree of induction during liver regeneration. We have investigated the function of each locus during L-ethionine-mediated AFP induction using adu...

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Veröffentlicht in:Somatic cell and molecular genetics 1988-11, Vol.14 (6), p.553-566
Hauptverfasser: MIFFLIN, R. C, MOLLER, P. C, PAPACONSTANTINOU, J
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PAPACONSTANTINOU, J
description Two genetic loci regulate hepatic alpha-fetoprotein (AFP) mRNA levels in adult mice. The raf locus controls basal levels and the Rif locus determines the degree of induction during liver regeneration. We have investigated the function of each locus during L-ethionine-mediated AFP induction using adult female mice with different Rif/raf genotypes. A single intraperitoneal injection of L-ethionine (0.5 mg/g body weight) resulted in significant triglyceride accumulation in hepatic parenchymal cells and increased AFP synthesis 48-96 h following injection. Hepatic AFP mRNA levels in Balb/cJ mice (high basal level/high induction level during regeneration) were 10- to 30-fold higher than Balb/cCRBL or C3H/He mice (low basal level/high induction level) following ethionine injection, indicating that raf-mediated differences persisted throughout the course of acute ethionine poisoning. The magnitude of this induction was similar to that seen during carbon tetrachloride-induced regeneration. In contrast, C57BL/6 mice (low basal level/low induction level during regeneration) contained hepatic AFP mRNA levels similar to Balb/cCRBL and C3H/He mice following ethionine injection. Thus, Rif-dependent differences seen during liver regeneration were not seen during acute ethionine poisoning. This leads us to conclude that (1) hepatic AFP mRNA induction by ethionine may not be mediated by the Rif locus if Rif is a transcriptional inducer, or (2) if Rif is a transcriptional repressor, it is inactivated equally in all strains during acute ethionine poisoning, unlike during liver regeneration. Hepatic albumin mRNA levels were not affected by ethionine treatment in vivo. L-Ethionine elevated AFP mRNA levels in primary mouse hepatocyte cultures; however, ethionine treatment also increased albumin mRNA levels in vitro.
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Hepatic AFP mRNA levels in Balb/cJ mice (high basal level/high induction level during regeneration) were 10- to 30-fold higher than Balb/cCRBL or C3H/He mice (low basal level/high induction level) following ethionine injection, indicating that raf-mediated differences persisted throughout the course of acute ethionine poisoning. The magnitude of this induction was similar to that seen during carbon tetrachloride-induced regeneration. In contrast, C57BL/6 mice (low basal level/low induction level during regeneration) contained hepatic AFP mRNA levels similar to Balb/cCRBL and C3H/He mice following ethionine injection. Thus, Rif-dependent differences seen during liver regeneration were not seen during acute ethionine poisoning. 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C</creatorcontrib><creatorcontrib>MOLLER, P. C</creatorcontrib><creatorcontrib>PAPACONSTANTINOU, J</creatorcontrib><title>Genetic analysis of L-ethionine-mediated induction of alpha-fetoprotein in mice</title><title>Somatic cell and molecular genetics</title><addtitle>Somat Cell Mol Genet</addtitle><description>Two genetic loci regulate hepatic alpha-fetoprotein (AFP) mRNA levels in adult mice. The raf locus controls basal levels and the Rif locus determines the degree of induction during liver regeneration. We have investigated the function of each locus during L-ethionine-mediated AFP induction using adult female mice with different Rif/raf genotypes. A single intraperitoneal injection of L-ethionine (0.5 mg/g body weight) resulted in significant triglyceride accumulation in hepatic parenchymal cells and increased AFP synthesis 48-96 h following injection. Hepatic AFP mRNA levels in Balb/cJ mice (high basal level/high induction level during regeneration) were 10- to 30-fold higher than Balb/cCRBL or C3H/He mice (low basal level/high induction level) following ethionine injection, indicating that raf-mediated differences persisted throughout the course of acute ethionine poisoning. The magnitude of this induction was similar to that seen during carbon tetrachloride-induced regeneration. In contrast, C57BL/6 mice (low basal level/low induction level during regeneration) contained hepatic AFP mRNA levels similar to Balb/cCRBL and C3H/He mice following ethionine injection. Thus, Rif-dependent differences seen during liver regeneration were not seen during acute ethionine poisoning. This leads us to conclude that (1) hepatic AFP mRNA induction by ethionine may not be mediated by the Rif locus if Rif is a transcriptional inducer, or (2) if Rif is a transcriptional repressor, it is inactivated equally in all strains during acute ethionine poisoning, unlike during liver regeneration. Hepatic albumin mRNA levels were not affected by ethionine treatment in vivo. L-Ethionine elevated AFP mRNA levels in primary mouse hepatocyte cultures; however, ethionine treatment also increased albumin mRNA levels in vitro.</description><subject>Albumins - genetics</subject><subject>alpha-Fetoproteins - genetics</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Carbon Tetrachloride Poisoning - physiopathology</subject><subject>Cells, Cultured</subject><subject>Chemical and Drug Induced Liver Injury - pathology</subject><subject>Chemical and Drug Induced Liver Injury - physiopathology</subject><subject>Ethionine - pharmacology</subject><subject>Ethionine - poisoning</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Liver - physiology</subject><subject>Liver Regeneration</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>RNA, Messenger - genetics</subject><subject>Time Factors</subject><issn>0740-7750</issn><issn>1572-9931</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkE1Lw0AQhhdRaq1evAs5iAchOpvNZpOjFluFQi96DpPdCV3JR81uDv33bjHU08C8D-8wD2O3HJ44gHp-XQGXQgoOZ2zOpUriohD8nM1BpRArJeGSXTn3DQB5LuSMzZI04xnAnG3X1JG3OsIOm4OzLurraBOT39m-sx3FLRmLnkxkOzNqH7ZHApv9DuOafL8fek-2C3HUWk3X7KLGxtHNNBfsa_X2uXyPN9v1x_JlE2uRJj7ORZoqU5ERdVaBKIzhkpJUc8w05jWaxFQcJc8QiRNUlSEpAl-niqRUJBbs4a833P8ZyfmytU5T02BH_ejKYEFxCE4W7PEP1EPv3EB1uR9si8Oh5FAe7ZX_9gJ8N7WOVXj8hE66Qn4_5eg0NvWAnbbuhGVZoYDn4hcR3ndu</recordid><startdate>19881101</startdate><enddate>19881101</enddate><creator>MIFFLIN, R. 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Psychology</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Liver - physiology</topic><topic>Liver Regeneration</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>RNA, Messenger - genetics</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MIFFLIN, R. C</creatorcontrib><creatorcontrib>MOLLER, P. C</creatorcontrib><creatorcontrib>PAPACONSTANTINOU, J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Somatic cell and molecular genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MIFFLIN, R. C</au><au>MOLLER, P. C</au><au>PAPACONSTANTINOU, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetic analysis of L-ethionine-mediated induction of alpha-fetoprotein in mice</atitle><jtitle>Somatic cell and molecular genetics</jtitle><addtitle>Somat Cell Mol Genet</addtitle><date>1988-11-01</date><risdate>1988</risdate><volume>14</volume><issue>6</issue><spage>553</spage><epage>566</epage><pages>553-566</pages><issn>0740-7750</issn><eissn>1572-9931</eissn><coden>SCMGDN</coden><abstract>Two genetic loci regulate hepatic alpha-fetoprotein (AFP) mRNA levels in adult mice. The raf locus controls basal levels and the Rif locus determines the degree of induction during liver regeneration. We have investigated the function of each locus during L-ethionine-mediated AFP induction using adult female mice with different Rif/raf genotypes. A single intraperitoneal injection of L-ethionine (0.5 mg/g body weight) resulted in significant triglyceride accumulation in hepatic parenchymal cells and increased AFP synthesis 48-96 h following injection. Hepatic AFP mRNA levels in Balb/cJ mice (high basal level/high induction level during regeneration) were 10- to 30-fold higher than Balb/cCRBL or C3H/He mice (low basal level/high induction level) following ethionine injection, indicating that raf-mediated differences persisted throughout the course of acute ethionine poisoning. The magnitude of this induction was similar to that seen during carbon tetrachloride-induced regeneration. In contrast, C57BL/6 mice (low basal level/low induction level during regeneration) contained hepatic AFP mRNA levels similar to Balb/cCRBL and C3H/He mice following ethionine injection. Thus, Rif-dependent differences seen during liver regeneration were not seen during acute ethionine poisoning. This leads us to conclude that (1) hepatic AFP mRNA induction by ethionine may not be mediated by the Rif locus if Rif is a transcriptional inducer, or (2) if Rif is a transcriptional repressor, it is inactivated equally in all strains during acute ethionine poisoning, unlike during liver regeneration. Hepatic albumin mRNA levels were not affected by ethionine treatment in vivo. L-Ethionine elevated AFP mRNA levels in primary mouse hepatocyte cultures; however, ethionine treatment also increased albumin mRNA levels in vitro.</abstract><cop>London</cop><cop>New York, NY</cop><pub>Plenum</pub><pmid>2461600</pmid><doi>10.1007/BF01535310</doi><tpages>14</tpages></addata></record>
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subjects Albumins - genetics
alpha-Fetoproteins - genetics
Animals
Biological and medical sciences
Blotting, Northern
Carbon Tetrachloride Poisoning - physiopathology
Cells, Cultured
Chemical and Drug Induced Liver Injury - pathology
Chemical and Drug Induced Liver Injury - physiopathology
Ethionine - pharmacology
Ethionine - poisoning
Fundamental and applied biological sciences. Psychology
Gene expression
Gene Expression Regulation
Liver - physiology
Liver Regeneration
Mice
Mice, Inbred BALB C
Molecular and cellular biology
Molecular genetics
RNA, Messenger - genetics
Time Factors
title Genetic analysis of L-ethionine-mediated induction of alpha-fetoprotein in mice
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