Association of Exon 1 Variants of NOEY2 Gene with Poly cystic Ovary Syndrome (PCOS) and Diabetes

Parichehr Karajibani, Abolhasan Rezaei
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Abstract

Methods: This study was conducted on 240 blood samples (1 each) from women in four groups: polycystic, diabetes, polycystic-diabetes, and control. Genomic DNA extraction was performed using the extraction kit, according to the protocol. A primer pair was designed and synthesized for the exon 1 sequence of the NOEY2 gene. After gene amplification by polymerase chain reaction (PCR) and evaluation of band quality, Sanger sequencing was performed on PCR products. Sequencing results were analyzed using Chromas, GeneRunner, and Alignment software, and statistical calculations were performed by SNPAlyze, SPSS, and Web-Assotest program. two and of nucleotides and in the region of a between affect the affinity to bind in certain transcription factors by allelic changes due to its location in the CTCF overlapping promoter region.
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NOEY2基因外显子1变异与多囊卵巢综合征(PCOS)和糖尿病的关系
方法:本研究收集了240份女性血样(各1份),分为四组:多囊、糖尿病、多囊合并糖尿病和对照组。根据方案,使用提取试剂盒进行基因组DNA提取。设计并合成了NOEY2基因外显子1序列的引物对。经聚合酶链反应(PCR)扩增基因并评价条带质量后,对PCR产物进行Sanger测序。测序结果使用Chromas、GeneRunner和Alignment软件进行分析,并使用SNPAlyze、SPSS和Web-Assotest程序进行统计计算。由于其位于CTCF重叠启动子区域,两个核苷酸和a之间的区域通过等位基因变化影响与某些转录因子结合的亲和力。
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