2型糖尿病患者富亮氨酸重复序列和鸟苷酸激酶结构域(LRGUK)基因特异性引物设计

M. Mushlih, Siti Nur Maghfiroh Tis’iyyah, C. S. Rini, Azizah Krismonita Sari
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引用次数: 1

摘要

糖尿病II型(DT2)是由环境和遗传两种因素引起的胰岛素功能紊乱(胰岛素抵抗)。先前的研究已经确定了区分DT2和非DT2患者的特定等位基因的存在。等位基因鉴定为富亮氨酸重复序列和鸟苷酸激酶结构域(LRGUK)基因。本研究的目的是设计一种特异的引物来扩增LRGUK基因。引物设计基于576 bp的核苷酸碱基,利用NCBI-Primer BLAST在5′方向和3′方向分别增加100 bp和100 bp。所产生的引物是根据8个标准来选择的。用6例DT2患者样本验证结果,并用琼脂糖凝胶可视化。分析结果表明,引物Forward 5’-TCCTACTCTGTGTCCTTCCTTG-3’和Reverse 5’-GTGGTGACAAGGAGG TTTGC-3’能够特异性扩增,扩增长度为687 bp。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Specific Primer Design of Leucine Rich Repeats and Guanylate Kinase Domain Containing (LRGUK) Genes in Type II Diabetes Mellitus Patients
Diabetes Mellitus type II (DT2) is a disorder of insulin function (insulin resistance) caused by 2 factors, i.e. environmental and genetic factors. Previous studies have identified the presence of specific alleles that differentiate between DT2 and non-DT2 sufferers. Identification of the allele indicated leucine rich repeats and guanylate kinase domain containing (LRGUK) gene. The aim of this research was to design a specific primer to amplify LRGUK gene. The primer design was based on a 576 bp nucleotide base and added 100 bp in the 5'  and 100 bp in the 3' direction using NCBI-Primer BLAST. The primers produced were selected based on eight criteria’s. The results were validated with 6 samples of DT2 patients and visualized using agarose gel. The results of the analysis showed that the primers Forward 5'-TCCTACTCTGTGTCCTTCCTTG-3' and Reverse 5'-GTGGTGACAAGGAGG TTTGC-3' were able to amplify specifically with a length of 687 bp.
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