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 in | Journal of lipid research Vol. 51; no. 1; pp. 103 - 111 |
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Main Authors | , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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 Access | Get full text |
ISSN | 0022-2275 1539-7262 1539-7262 |
DOI | 10.1194/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. |
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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 |
AuthorAffiliation_xml | – name: Sahlgrenska School of Public Health and Community Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden – name: Division of Clinical Chemistry, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden – name: Sahlgrenska Center for Cardiovascular and Metabolic Research, Wallenberg Laboratory, University of Gothenburg, Gothenburg, Sweden – name: Department of Biostatistics, Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, Oslo, Norway – name: Department of Cardiothoracic Surgery and Anaesthesia, Karolinska University Hospital, Stockholm Sweden – name: Department of Medicine, Division of Diabetes, University of Helsinki, Helsinki, Finland – name: Department of Clinical Biochemistry, Rigshospitalet, and Department of Biomedical Science, University of Copenhagen Copenhagen Denmark – name: Atherosclerosis Research Unit, Department of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden |
Author_xml | – sequence: 1 givenname: Anna surname: Aminoff fullname: Aminoff, Anna organization: Atherosclerosis Research Unit, Department of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden – sequence: 2 givenname: Helena surname: Ledmyr fullname: Ledmyr, Helena organization: Atherosclerosis Research Unit, Department of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden – sequence: 3 givenname: Petra surname: Thulin fullname: Thulin, Petra organization: Atherosclerosis Research Unit, Department of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden – sequence: 4 givenname: Kerstin surname: Lundell fullname: Lundell, Kerstin organization: Atherosclerosis Research Unit, Department of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden – sequence: 5 givenname: Leyla surname: Nunez fullname: Nunez, Leyla organization: Sahlgrenska School of Public Health and Community Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden – sequence: 6 givenname: Elisabeth surname: Strandhagen fullname: Strandhagen, Elisabeth organization: Sahlgrenska School of Public Health and Community Medicine, Institute of Medicine, University of Gothenburg, Gothenburg, Sweden – sequence: 7 givenname: Charlotte surname: Murphy fullname: Murphy, Charlotte organization: Division of Clinical Chemistry, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden – sequence: 8 givenname: Ulf surname: Lidberg fullname: Lidberg, Ulf organization: Sahlgrenska Center for Cardiovascular and Metabolic Research, Wallenberg Laboratory, University of Gothenburg, Gothenburg, Sweden – sequence: 9 givenname: Jukka surname: Westerbacka fullname: Westerbacka, Jukka organization: Department of Medicine, Division of Diabetes, University of Helsinki, Helsinki, Finland – sequence: 10 givenname: Anders surname: Franco-Cereceda fullname: Franco-Cereceda, Anders organization: Department of Cardiothoracic Surgery and Anaesthesia, Karolinska University Hospital, Stockholm Sweden – sequence: 11 givenname: Jan surname: Liska fullname: Liska, Jan organization: Department of Cardiothoracic Surgery and Anaesthesia, Karolinska University Hospital, Stockholm Sweden – sequence: 12 givenname: Lars Bo surname: Nielsen fullname: Nielsen, Lars Bo organization: Department of Clinical Biochemistry, Rigshospitalet, and Department of Biomedical Science, University of Copenhagen Copenhagen Denmark – sequence: 13 givenname: Mats surname: Gåfvels fullname: Gåfvels, Mats organization: Division of Clinical Chemistry, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden – sequence: 14 givenname: Maria Nastase surname: Mannila fullname: Mannila, Maria Nastase organization: Atherosclerosis Research Unit, Department of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden – sequence: 15 givenname: Anders surname: Hamsten fullname: Hamsten, Anders organization: Atherosclerosis Research Unit, Department of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden – sequence: 16 givenname: Hannele surname: Yki-Järvinen fullname: Yki-Järvinen, Hannele organization: Department of Medicine, Division of Diabetes, University of Helsinki, Helsinki, Finland – sequence: 17 givenname: Dag surname: Thelle fullname: Thelle, Dag organization: Department of Biostatistics, Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, Oslo, Norway – sequence: 18 givenname: Per surname: Eriksson fullname: Eriksson, Per organization: Atherosclerosis Research Unit, Department of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden – sequence: 19 givenname: Jan surname: Borén fullname: Borén, Jan organization: Sahlgrenska Center for Cardiovascular and Metabolic Research, Wallenberg Laboratory, University of Gothenburg, Gothenburg, Sweden – sequence: 20 givenname: Ewa surname: Ehrenborg fullname: Ehrenborg, Ewa email: Ewa.Ehrenborg@ki.se organization: Atherosclerosis Research Unit, Department of Medicine, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden |
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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] |
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