Specific Primer Design of Leucine Rich Repeats and Guanylate Kinase Domain Containing (LRGUK) Genes in Type II Diabetes Mellitus Patients

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

Abstract

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.
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
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。
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