Allele-specific regulation of MTTP expression influences the risk of ischemic heart disease[S]

Promoter polymorphisms in microsomal triglyceride transfer protein (MTTP) have been associated with decreased plasma lipids but an increased risk for ischemic heart disease (IHD), indicating that MTTP influences the susceptibility for IHD independent of plasma lipids. The objective of this study was...

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Published inJournal of lipid research Vol. 51; no. 1; pp. 103 - 111
Main Authors Aminoff, Anna, Ledmyr, Helena, Thulin, Petra, Lundell, Kerstin, Nunez, Leyla, Strandhagen, Elisabeth, Murphy, Charlotte, Lidberg, Ulf, Westerbacka, Jukka, Franco-Cereceda, Anders, Liska, Jan, Nielsen, Lars Bo, Gåfvels, Mats, Mannila, Maria Nastase, Hamsten, Anders, Yki-Järvinen, Hannele, Thelle, Dag, Eriksson, Per, Borén, Jan, Ehrenborg, Ewa
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.01.2010
American Society for Biochemistry and Molecular Biology
The American Society for Biochemistry and Molecular Biology
Elsevier
Subjects
Online AccessGet full text
ISSN0022-2275
1539-7262
1539-7262
DOI10.1194/jlr.M900195-JLR200

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Abstract Promoter polymorphisms in microsomal triglyceride transfer protein (MTTP) have been associated with decreased plasma lipids but an increased risk for ischemic heart disease (IHD), indicating that MTTP influences the susceptibility for IHD independent of plasma lipids. The objective of this study was to characterize the functional promoter polymorphism in MTTP predisposing to IHD and its underlying mechanism. Use of pyrosequencing technology revealed that presence of the minor alleles of the promoter polymorphisms -493G>T and -164T>C result in lower transcription of MTTP in vivo in the heart, liver, and macrophages. In vitro experiments indicated that the minor -164C allele mediates the lower gene expression and that C/EBP binds to the polymorphic region in an allele-specific manner. Furthermore, homozygous carriers of the -164C were found to have increased risk for IHD as shown in a case-control study including a total of 544 IHD patients and 544 healthy control subjects. We concluded that carriers of the minor -164C allele have lower expression of MTTP in the heart, mediated at least partly by the transcription factor CCAAT/enhancer binding protein, and that reduced concentration of MTTP in the myocardium may contribute to IHD upon ischemic damage.
AbstractList Promoter polymorphisms in microsomal triglyceride transfer protein (MTTP) have been associated with decreased plasma lipids but an increased risk for ischemic heart disease (IHD), indicating that MTTP influences the susceptibility for IHD independent of plasma lipids. The objective of this study was to characterize the functional promoter polymorphism in MTTP predisposing to IHD and its underlying mechanism. Use of pyrosequencing technology revealed that presence of the minor alleles of the promoter polymorphisms -493G>T and -164T>C result in lower transcription of MTTP in vivo in the heart, liver, and macrophages. In vitro experiments indicated that the minor -164C allele mediates the lower gene expression and that C/EBP binds to the polymorphic region in an allele-specific manner. Furthermore, homozygous carriers of the -164C were found to have increased risk for IHD as shown in a case-control study including a total of 544 IHD patients and 544 healthy control subjects. We concluded that carriers of the minor -164C allele have lower expression of MTTP in the heart, mediated at least partly by the transcription factor CCAAT/enhancer binding protein, and that reduced concentration of MTTP in the myocardium may contribute to IHD upon ischemic damage.
Promoter polymorphisms in microsomal triglyceride transfer protein ( MTTP ) have been associated with decreased plasma lipids but an increased risk for ischemic heart disease (IHD), indicating that MTTP influences the susceptibility for IHD independent of plasma lipids. The objective of this study was to characterize the functional promoter polymorphism in MTTP predisposing to IHD and its underlying mechanism. Use of pyrosequencing technology revealed that presence of the minor alleles of the promoter polymorphisms -493G>T and -164T>C result in lower transcription of MTTP in vivo in the heart, liver, and macrophages. In vitro experiments indicated that the minor -164C allele mediates the lower gene expression and that C/EBP binds to the polymorphic region in an allele-specific manner. Furthermore, homozygous carriers of the -164C were found to have increased risk for IHD as shown in a case-control study including a total of 544 IHD patients and 544 healthy control subjects. We concluded that carriers of the minor -164C allele have lower expression of MTTP in the heart, mediated at least partly by the transcription factor CCAAT/enhancer binding protein, and that reduced concentration of MTTP in the myocardium may contribute to IHD upon ischemic damage.
Promoter polymorphisms in microsomal triglyceride transfer protein (MTTP) have been associated with decreased plasma lipids but an increased risk for ischemic heart disease (IHD), indicating that MTTP influences the susceptibility for IHD independent of plasma lipids. The objective of this study was to characterize the functional promoter polymorphism in MTTP predisposing to IHD and its underlying mechanism. Use of pyrosequencing technology revealed that presence of the minor alleles of the promoter polymorphisms -493G>T and -164T>C result in lower transcription of MTTP in vivo in the heart, liver, and macrophages. In vitro experiments indicated that the minor -164C allele mediates the lower gene expression and that C/EBP binds to the polymorphic region in an allele-specific manner. Furthermore, homozygous carriers of the -164C were found to have increased risk for IHD as shown in a case-control study including a total of 544 IHD patients and 544 healthy control subjects. We concluded that carriers of the minor -164C allele have lower expression of MTTP in the heart, mediated at least partly by the transcription factor CCAAT/enhancer binding protein, and that reduced concentration of MTTP in the myocardium may contribute to IHD upon ischemic damage.Promoter polymorphisms in microsomal triglyceride transfer protein (MTTP) have been associated with decreased plasma lipids but an increased risk for ischemic heart disease (IHD), indicating that MTTP influences the susceptibility for IHD independent of plasma lipids. The objective of this study was to characterize the functional promoter polymorphism in MTTP predisposing to IHD and its underlying mechanism. Use of pyrosequencing technology revealed that presence of the minor alleles of the promoter polymorphisms -493G>T and -164T>C result in lower transcription of MTTP in vivo in the heart, liver, and macrophages. In vitro experiments indicated that the minor -164C allele mediates the lower gene expression and that C/EBP binds to the polymorphic region in an allele-specific manner. Furthermore, homozygous carriers of the -164C were found to have increased risk for IHD as shown in a case-control study including a total of 544 IHD patients and 544 healthy control subjects. We concluded that carriers of the minor -164C allele have lower expression of MTTP in the heart, mediated at least partly by the transcription factor CCAAT/enhancer binding protein, and that reduced concentration of MTTP in the myocardium may contribute to IHD upon ischemic damage.
Author Franco-Cereceda, Anders
Ehrenborg, Ewa
Gåfvels, Mats
Borén, Jan
Aminoff, Anna
Nunez, Leyla
Thulin, Petra
Lundell, Kerstin
Mannila, Maria Nastase
Eriksson, Per
Ledmyr, Helena
Westerbacka, Jukka
Lidberg, Ulf
Liska, Jan
Yki-Järvinen, Hannele
Thelle, Dag
Nielsen, Lars Bo
Strandhagen, Elisabeth
Hamsten, Anders
Murphy, Charlotte
AuthorAffiliation Department of Medicine, Division of Diabetes, University of Helsinki, Helsinki, Finland
Sahlgrenska Center for Cardiovascular and Metabolic Research, Wallenberg Laboratory, University of Gothenburg, Gothenburg, Sweden
Department of Cardiothoracic Surgery and Anaesthesia, Karolinska University Hospital, Stockholm Sweden
Department of Biostatistics, Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, Oslo, Norway
Sahlgrenska School of Public Health and Community Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden
Atherosclerosis Research Unit, Department of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden
Department of Clinical Biochemistry, Rigshospitalet, and Department of Biomedical Science, University of Copenhagen Copenhagen Denmark
Division of Clinical Chemistry, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden
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Issue 1
Keywords promoter activity
myocardium
lipid accumulation
lipotoxicity
Language English
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Snippet Promoter polymorphisms in microsomal triglyceride transfer protein (MTTP) have been associated with decreased plasma lipids but an increased risk for ischemic...
Promoter polymorphisms in microsomal triglyceride transfer protein ( MTTP ) have been associated with decreased plasma lipids but an increased risk for...
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pubmedcentral
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pubmed
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Open Access Repository
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Enrichment Source
Publisher
StartPage 103
SubjectTerms Aged
Alleles
Base Sequence
Cardiology and Cardiovascular Disease
Carrier Proteins
Carrier Proteins - genetics
Case-Control Studies
CCAAT-Enhancer-Binding Proteins
CCAAT-Enhancer-Binding Proteins - genetics
CCAAT-Enhancer-Binding Proteins - metabolism
Fatty Liver
Fatty Liver - genetics
Fatty Liver - metabolism
Female
Gene Expression Regulation
Genetic
genetics
Heart
Heart - physiology
HeLa Cells
Humans
Kardiologi och kardiovaskulära sjukdomar
lipid accumulation
lipotoxicity
Liver
Liver - metabolism
Macrophages
Macrophages - metabolism
Male
metabolism
Middle Aged
Monocytes
Monocytes - metabolism
Myocardial Ischemia
Myocardial Ischemia - genetics
myocardium
physiology
Polymorphism
Polymorphism, Single Nucleotide
promoter activity
Promoter Regions
Promoter Regions, Genetic
Response Elements
Response Elements - genetics
Single Nucleotide
Title Allele-specific regulation of MTTP expression influences the risk of ischemic heart disease[S]
URI https://dx.doi.org/10.1194/jlr.M900195-JLR200
https://www.ncbi.nlm.nih.gov/pubmed/19546343
https://www.proquest.com/docview/46457421
https://www.proquest.com/docview/734196034
https://pubmed.ncbi.nlm.nih.gov/PMC2789770
https://gup.ub.gu.se/publication/133294
http://kipublications.ki.se/Default.aspx?queryparsed=id:119738298
https://doaj.org/article/80621397cadc4995a25c7794e779b1af
Volume 51
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