Regulation of rDNA Transcription During Endothelin-1--Induced Hypertrophy of Neonatal Cardiomyocytes: Hyperphosphorylation of Upstream Binding Factor, an rDNA Transcription Factor

Treatment of cultured neonatal cardiomyocytes with endothelin-1 and phorbol 12-myristate 13-acetate (PMA) results in cardiomyocyte hypertrophy. However, the signal transduction pathways involved in this process are poorly understood. Because increased ribosome biogenesis is a requisite for hypertrop...

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Veröffentlicht in:Circulation research 1996-03, Vol.78 (3), p.354-361
Hauptverfasser: Luyken, Joachim, Hannan, Ross D, Cheung, Joseph Y, Rothblum, Lawrence I
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container_title Circulation research
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creator Luyken, Joachim
Hannan, Ross D
Cheung, Joseph Y
Rothblum, Lawrence I
description Treatment of cultured neonatal cardiomyocytes with endothelin-1 and phorbol 12-myristate 13-acetate (PMA) results in cardiomyocyte hypertrophy. However, the signal transduction pathways involved in this process are poorly understood. Because increased ribosome biogenesis is a requisite for hypertrophy, we sought to (1) confirm the hypothesis that these two hypertrophic agents did indeed induce rRNA synthesis and (2) examine the mechanism through which this induction was accomplished. In this study, hypertrophy of contraction-arrested neonatal cardiomyocytes induced by treatment with either endothelin-1 or PMA was associated with increased rDNA transcription. Western blots demonstrated that the enhanced rates of rDNA transcription were not mediated by increased amounts of either RNA polymerase I or upstream binding factor (UBF), an rDNA transcription factor. However, immunoprecipitation of [sup 32 P]orthophosphate-labeled UBF from hypertrophying neonatal cardiomyocytes suggested that the increased rate of rDNA transcription may be due to the hyperphosphorylation of UBF, which would increase the activity of UBF. The increase in UBF phosphorylation occurred within 3 to 6 hours after exposure to either agent, was maximal at 12 hours, and was sustained for at least the first 24 hours of exposure. Phosphoamino acid analysis of UBF immunoprecipitated from control and treated cardiomyocytes demonstrated that UBF was phosphorylated exclusively on serine residues. Our previous studies have shown that the cellular UBF content increased in adrenergic- and contraction-induced models of cardiac hypertrophy. This study with endothelin-1 and PMA demonstrates that the modulation of UBF phosphorylation is an additional pathway by which ribosome biogenesis may be regulated in neonatal cardiomyocytes. These results support the hypothesis that UBF is an important regulatory factor during the initiation and maintenance of the accelerated rate of rDNA transcription observed during neonatal cardiomyocyte hypertrophy mediated by both phorbol esters and endothelin-1.(Circ Res. 1996;78:354-361.)
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However, the signal transduction pathways involved in this process are poorly understood. Because increased ribosome biogenesis is a requisite for hypertrophy, we sought to (1) confirm the hypothesis that these two hypertrophic agents did indeed induce rRNA synthesis and (2) examine the mechanism through which this induction was accomplished. In this study, hypertrophy of contraction-arrested neonatal cardiomyocytes induced by treatment with either endothelin-1 or PMA was associated with increased rDNA transcription. Western blots demonstrated that the enhanced rates of rDNA transcription were not mediated by increased amounts of either RNA polymerase I or upstream binding factor (UBF), an rDNA transcription factor. However, immunoprecipitation of [sup 32 P]orthophosphate-labeled UBF from hypertrophying neonatal cardiomyocytes suggested that the increased rate of rDNA transcription may be due to the hyperphosphorylation of UBF, which would increase the activity of UBF. The increase in UBF phosphorylation occurred within 3 to 6 hours after exposure to either agent, was maximal at 12 hours, and was sustained for at least the first 24 hours of exposure. Phosphoamino acid analysis of UBF immunoprecipitated from control and treated cardiomyocytes demonstrated that UBF was phosphorylated exclusively on serine residues. Our previous studies have shown that the cellular UBF content increased in adrenergic- and contraction-induced models of cardiac hypertrophy. This study with endothelin-1 and PMA demonstrates that the modulation of UBF phosphorylation is an additional pathway by which ribosome biogenesis may be regulated in neonatal cardiomyocytes. 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However, the signal transduction pathways involved in this process are poorly understood. Because increased ribosome biogenesis is a requisite for hypertrophy, we sought to (1) confirm the hypothesis that these two hypertrophic agents did indeed induce rRNA synthesis and (2) examine the mechanism through which this induction was accomplished. In this study, hypertrophy of contraction-arrested neonatal cardiomyocytes induced by treatment with either endothelin-1 or PMA was associated with increased rDNA transcription. Western blots demonstrated that the enhanced rates of rDNA transcription were not mediated by increased amounts of either RNA polymerase I or upstream binding factor (UBF), an rDNA transcription factor. However, immunoprecipitation of [sup 32 P]orthophosphate-labeled UBF from hypertrophying neonatal cardiomyocytes suggested that the increased rate of rDNA transcription may be due to the hyperphosphorylation of UBF, which would increase the activity of UBF. The increase in UBF phosphorylation occurred within 3 to 6 hours after exposure to either agent, was maximal at 12 hours, and was sustained for at least the first 24 hours of exposure. Phosphoamino acid analysis of UBF immunoprecipitated from control and treated cardiomyocytes demonstrated that UBF was phosphorylated exclusively on serine residues. Our previous studies have shown that the cellular UBF content increased in adrenergic- and contraction-induced models of cardiac hypertrophy. This study with endothelin-1 and PMA demonstrates that the modulation of UBF phosphorylation is an additional pathway by which ribosome biogenesis may be regulated in neonatal cardiomyocytes. 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Vascular system</subject><subject>Cardiomegaly - chemically induced</subject><subject>Cardiomegaly - genetics</subject><subject>Cardiomegaly - metabolism</subject><subject>Cells, Cultured</subject><subject>DNA, Ribosomal - metabolism</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Endothelins - pharmacology</subject><subject>Heart</subject><subject>Heart failure, cardiogenic pulmonary edema, cardiac enlargement</subject><subject>Medical sciences</subject><subject>Myocardium - metabolism</subject><subject>Phosphorylation</subject><subject>Pol1 Transcription Initiation Complex Proteins</subject><subject>Protein Kinase C - antagonists &amp; inhibitors</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>RNA Polymerase I - metabolism</subject><subject>Tetradecanoylphorbol Acetate - pharmacology</subject><subject>Transcription Factors - metabolism</subject><subject>Transcription, Genetic</subject><issn>0009-7330</issn><issn>1524-4571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptUUtv1DAQthCoLIUzJ6QcOOIwfiSOubXb7UOqilTa82oSO00ga0e2oyq_iz9ItruCC4fRjL7vmzchHxnkjJXsK7D8fvMjV1UuclHIV2TFCi6pLBR7TVYAoKkSAt6SdzH-BGBScH1CTqpCi1KLFfl9b5-mAVPvXebbLFzcnWUPAV1sQj--oBdT6N1TtnHGp84OvaOM0htnpsaa7HoebUjBj928T7-z3mHCIVtjML3fzb6Zk43fDrqx83GxMP_r9zjGFCzusvPemX2bS2ySD18ydP-b5cC-J29aHKL9cPSn5PFy87C-prffr27WZ7d05BVwWgqzrItFzSqsFQJTWmgmUSvdmkpVrFZFU1slNLSGAdZoWskloqktRwHilHw61B2nemfNdgz9DsO8PR5v4T8feYwNDu0yatPHvzIBUHKQi0weZM9-SDbEX8P0bMO2szikbru8CAQwTpnW5RIB0D3ExR9SG5FL</recordid><startdate>199603</startdate><enddate>199603</enddate><creator>Luyken, Joachim</creator><creator>Hannan, Ross D</creator><creator>Cheung, Joseph Y</creator><creator>Rothblum, Lawrence I</creator><general>American Heart Association, Inc</general><general>Lippincott</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>199603</creationdate><title>Regulation of rDNA Transcription During Endothelin-1--Induced Hypertrophy of Neonatal Cardiomyocytes: Hyperphosphorylation of Upstream Binding Factor, an rDNA Transcription Factor</title><author>Luyken, Joachim ; Hannan, Ross D ; Cheung, Joseph Y ; Rothblum, Lawrence I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p2802-63d143a5b18ab7a01793914a979fd8781b75cbe7390fd10abadf424aadbe2a303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Biological and medical sciences</topic><topic>Cardiology. Vascular system</topic><topic>Cardiomegaly - chemically induced</topic><topic>Cardiomegaly - genetics</topic><topic>Cardiomegaly - metabolism</topic><topic>Cells, Cultured</topic><topic>DNA, Ribosomal - metabolism</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Endothelins - pharmacology</topic><topic>Heart</topic><topic>Heart failure, cardiogenic pulmonary edema, cardiac enlargement</topic><topic>Medical sciences</topic><topic>Myocardium - metabolism</topic><topic>Phosphorylation</topic><topic>Pol1 Transcription Initiation Complex Proteins</topic><topic>Protein Kinase C - antagonists &amp; inhibitors</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>RNA Polymerase I - metabolism</topic><topic>Tetradecanoylphorbol Acetate - pharmacology</topic><topic>Transcription Factors - metabolism</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luyken, Joachim</creatorcontrib><creatorcontrib>Hannan, Ross D</creatorcontrib><creatorcontrib>Cheung, Joseph Y</creatorcontrib><creatorcontrib>Rothblum, Lawrence I</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Circulation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luyken, Joachim</au><au>Hannan, Ross D</au><au>Cheung, Joseph Y</au><au>Rothblum, Lawrence I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of rDNA Transcription During Endothelin-1--Induced Hypertrophy of Neonatal Cardiomyocytes: Hyperphosphorylation of Upstream Binding Factor, an rDNA Transcription Factor</atitle><jtitle>Circulation research</jtitle><addtitle>Circ Res</addtitle><date>1996-03</date><risdate>1996</risdate><volume>78</volume><issue>3</issue><spage>354</spage><epage>361</epage><pages>354-361</pages><issn>0009-7330</issn><eissn>1524-4571</eissn><coden>CIRUAL</coden><abstract>Treatment of cultured neonatal cardiomyocytes with endothelin-1 and phorbol 12-myristate 13-acetate (PMA) results in cardiomyocyte hypertrophy. However, the signal transduction pathways involved in this process are poorly understood. Because increased ribosome biogenesis is a requisite for hypertrophy, we sought to (1) confirm the hypothesis that these two hypertrophic agents did indeed induce rRNA synthesis and (2) examine the mechanism through which this induction was accomplished. In this study, hypertrophy of contraction-arrested neonatal cardiomyocytes induced by treatment with either endothelin-1 or PMA was associated with increased rDNA transcription. Western blots demonstrated that the enhanced rates of rDNA transcription were not mediated by increased amounts of either RNA polymerase I or upstream binding factor (UBF), an rDNA transcription factor. However, immunoprecipitation of [sup 32 P]orthophosphate-labeled UBF from hypertrophying neonatal cardiomyocytes suggested that the increased rate of rDNA transcription may be due to the hyperphosphorylation of UBF, which would increase the activity of UBF. The increase in UBF phosphorylation occurred within 3 to 6 hours after exposure to either agent, was maximal at 12 hours, and was sustained for at least the first 24 hours of exposure. Phosphoamino acid analysis of UBF immunoprecipitated from control and treated cardiomyocytes demonstrated that UBF was phosphorylated exclusively on serine residues. Our previous studies have shown that the cellular UBF content increased in adrenergic- and contraction-induced models of cardiac hypertrophy. This study with endothelin-1 and PMA demonstrates that the modulation of UBF phosphorylation is an additional pathway by which ribosome biogenesis may be regulated in neonatal cardiomyocytes. These results support the hypothesis that UBF is an important regulatory factor during the initiation and maintenance of the accelerated rate of rDNA transcription observed during neonatal cardiomyocyte hypertrophy mediated by both phorbol esters and endothelin-1.(Circ Res. 1996;78:354-361.)</abstract><cop>Hagerstown, MD</cop><pub>American Heart Association, Inc</pub><pmid>8593693</pmid><doi>10.1161/01.RES.78.3.354</doi><tpages>8</tpages></addata></record>
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source MEDLINE; American Heart Association Journals; Journals@Ovid Complete; EZB-FREE-00999 freely available EZB journals
subjects Animals
Animals, Newborn
Biological and medical sciences
Cardiology. Vascular system
Cardiomegaly - chemically induced
Cardiomegaly - genetics
Cardiomegaly - metabolism
Cells, Cultured
DNA, Ribosomal - metabolism
DNA-Binding Proteins - metabolism
Endothelins - pharmacology
Heart
Heart failure, cardiogenic pulmonary edema, cardiac enlargement
Medical sciences
Myocardium - metabolism
Phosphorylation
Pol1 Transcription Initiation Complex Proteins
Protein Kinase C - antagonists & inhibitors
Rats
Rats, Sprague-Dawley
RNA Polymerase I - metabolism
Tetradecanoylphorbol Acetate - pharmacology
Transcription Factors - metabolism
Transcription, Genetic
title Regulation of rDNA Transcription During Endothelin-1--Induced Hypertrophy of Neonatal Cardiomyocytes: Hyperphosphorylation of Upstream Binding Factor, an rDNA Transcription Factor
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