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Chin. med. j ; Chin. med. j;(24): 753-758, 2002.
Artigo em Inglês | WPRIM | ID: wpr-340421

RESUMO

<p><b>OBJECTIVE</b>To investigate the role of a potential diabetes-related mitochondrial region, which includes two previously reported mutations, 3243A-->G and 3316G-->A, in Chinese patients with adult-onset type 2 diabetes.</p><p><b>METHODS</b>A total of 277 patients and 241 normal subjects were recruited for the study. Mitochondrial nt 3116 - 3353, which spans the 16S rRNA, tRNA(leu(UUR)) and the NADH dehydrogenase 1 gene, were detected using polymerase chain reaction (PCR), direct DNA sequencing, PCR-restriction fragment length polymorphism and allele-specific PCR. Variants were analyzed by two-tailed Fisher exact test. The function of the variants in 16S rRNA were predicted for minimal free energy secondary structures by RNA folding software mfold version 3.</p><p><b>RESULTS</b>Four homoplasmic nucleotide substitutions were observed, 3200T-->C, 3206C-->T, 3290T-->C and 3316G-->A. Only the 3200T-->C mutation is present in the diabetic population and absent in the control population. No statistically significant associations were found between the other three variants and type 2 diabetes. The 3200T-->C and 3206C-->T nucleotide substitutions located in 16S rRNA are novel variants. The 3200T-->C caused a great alteration in the minimal free energy secondary structure model while the 3206C-->T altered normal 16S rRNA structure little.</p><p><b>CONCLUSIONS</b>The results suggest that the 3200T-->C mutation is linked to the development of type 2 diabetes, but that the other observed mutations are neutral. In contrast to the Japanese studies, the 3316G-->A does not appear to be related to type 2 diabetes.</p>


Assuntos
Idoso , Humanos , Pessoa de Meia-Idade , Idade de Início , Alelos , Sequência de Bases , Análise Mutacional de DNA , DNA Mitocondrial , Química , Genética , Diabetes Mellitus Tipo 2 , Genética , Modelos Moleculares , Conformação de Ácido Nucleico , Mutação Puntual , Reação em Cadeia da Polimerase , Métodos , Polimorfismo de Fragmento de Restrição , RNA Ribossômico 16S , Química , Genética
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