HOROVA, Eva, Michal PRAZNY, Kateřina KAŇKOVÁ, K. BRISMAR a H. F. GU. Genetic and Functional Analyses of MRAS and HNF1A Genes in Diabetes and Diabetic Nephropathy. Folia biologica. Praha: Institute of Molecular Genetics, 2012, roč. 58, č. 3, s. 121-127. ISSN 0015-5500.
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Základní údaje
Originální název Genetic and Functional Analyses of MRAS and HNF1A Genes in Diabetes and Diabetic Nephropathy
Název česky Genetic and Functional Analyses of MRAS and HNF1A Genes in Diabetes and Diabetic Nephropathy
Autoři HOROVA, Eva (203 Česká republika), Michal PRAZNY (203 Česká republika), Kateřina KAŇKOVÁ (203 Česká republika, garant, domácí), K. BRISMAR (752 Švédsko) a H. F. GU (752 Švédsko).
Vydání Folia biologica, Praha, Institute of Molecular Genetics, 2012, 0015-5500.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30202 Endocrinology and metabolism
Stát vydavatele Česká republika
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 1.219
Kód RIV RIV/00216224:14110/12:00064926
Organizační jednotka Lékařská fakulta
UT WoS 000306098400005
Klíčová slova česky MRAS; HNF1A; diabetic nephropathy; type 1 and 2 diabetes
Klíčová slova anglicky MRAS; HNF1A; diabetic nephropathy; type 1 and 2 diabetes
Změnil Změnila: prof. MUDr. Kateřina Kaňková, Ph.D., učo 2524. Změněno: 4. 12. 2012 15:30.
Anotace
Evidence has recently indicated that the MRAS and HNF1A genetic polymorphisms are associated with coronary artery disease. The MRAS and HNF1A genes are located on chromosomes 3q and 12q within the regions where associations with diabetes and diabetic nephropathy occur. We thus performed genetic and functional analyses of these two genes to evaluate their impacts on diabetes and diabetic nephropathy. MRAS and HNF1A genetic polymorphisms were genotyped in 1399 Czech subjects including non-diabetic controls (339), type 1 (243) and type 2 (817) diabetic patients with and without diabetic nephropathy using TaqMan allelic discrimination. Gene expression levels in the kidneys of diabetic Goto-Kakizaki and Wistar rats were detected with real-time RT-PCR. Despite no significance in genetic analysis of diabetic subjects, SNP rs2259816 in the HNF1A gene tended to associate with diabetic nephropathy in type 1 diabetic patients. The hnf1a gene expression was significantly decreased in kidney tissues of Goto-Kakizaki rats compared to Wistar and insulin-treated Goto-Kakizaki rats. There was neither significant association in the MRAS genetic polymorphism with diabetic nephropathy nor variation of mras gene expression in the kidneys of Goto-Kakizaki and Wistar rats. Data from the present study have not proved any significant association of the MRAS and HNF1A genetic polymorphisms with diabetes and diabetic nephropathy in a cohort of Czech population. However, the functional analysis and the trend in genetic analysis suggest that the HNF1A gene may have primary genetic impact on the development of diabetic nephropathy.
Anotace česky
Evidence has recently indicated that the MRAS and HNF1A genetic polymorphisms are associated with coronary artery disease. The MRAS and HNF1A genes are located on chromosomes 3q and 12q within the regions where associations with diabetes and diabetic nephropathy occur. We thus performed genetic and functional analyses of these two genes to evaluate their impacts on diabetes and diabetic nephropathy. MRAS and HNF1A genetic polymorphisms were genotyped in 1399 Czech subjects including non-diabetic controls (339), type 1 (243) and type 2 (817) diabetic patients with and without diabetic nephropathy using TaqMan allelic discrimination. Gene expression levels in the kidneys of diabetic Goto-Kakizaki and Wistar rats were detected with real-time RT-PCR. Despite no significance in genetic analysis of diabetic subjects, SNP rs2259816 in the HNF1A gene tended to associate with diabetic nephropathy in type 1 diabetic patients. The hnf1a gene expression was significantly decreased in kidney tissues of Goto-Kakizaki rats compared to Wistar and insulin-treated Goto-Kakizaki rats. There was neither significant association in the MRAS genetic polymorphism with diabetic nephropathy nor variation of mras gene expression in the kidneys of Goto-Kakizaki and Wistar rats. Data from the present study have not proved any significant association of the MRAS and HNF1A genetic polymorphisms with diabetes and diabetic nephropathy in a cohort of Czech population. However, the functional analysis and the trend in genetic analysis suggest that the HNF1A gene may have primary genetic impact on the development of diabetic nephropathy.
Návaznosti
NT11405, projekt VaVNázev: Mikrobiologické a genetické determinanty rozvoje a progrese parodontitidy u diabetiků 1. a 2. typu a jejich reciproční vztah ke kompenzaci diabetu
Investor: Ministerstvo zdravotnictví ČR, Mikrobiologické a genetické determinanty rozvoje a progrese parodontitidy u diabetiků 1. a 2. typu a jejich reciproční vztah ke kompenzaci diabetu
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