Published in: Third International Private Medical Congress of Iran
COI code: IPMCMED03_067
Paper Language: English
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Authors The identification of Mutations in exon1 of NKX2.6 gene in patients with Congenital Heart DefectsDonya Ghazi - Department of Biology, Faculty of science, Yazd University, Yazd, Iran
Mehri Khatami - Department of Biology, Faculty of science, Yazd University, Yazd, Iran
Mohammad Mehdi Heidari - Department of Biology, Faculty of science, Yazd University, Yazd, Iran
Abstract:Introduction: CHD results from perturbation of the normal program of cardiac development. it is the most common congenital anomaly in newborn babies. CHD is multifactorial, due to both genetic predisposition and environmental influences. NKX2-6 gene encodes a homeobox-containing protein that belongs to the NK-2 homeobox family. This gene plays an important role in the development of the cardiovascular system. Mutations in this gene are associated with CHDs, especially conotruncal defects such as persistent truncus arteriosus. Method: we analyzed the Nucleotide changes in exon 1 of NKX2.6 gene in patients suffering from congenital heart diseases in the province of YAZD. The PCR-SSCP and DNA sequencing methods used to detect the mutation of NKX2.6 gene in 110 pediatric patients with CHDs. We also used Polyphen-2 and Psipred databases and Pymol software to predict the effect of mutation detected on the structure and function of the NKX2.6 protein.Results: One heterozygous nucleotide replacement at c.109A> T position with amino acid change (S37C) were observed in one pediatric patient. Pymol results show that this mutation change the number and length of hydrogen bonds. Polyohen-2 result show that S37C amino acid change is benign and the results obtained from Psipred website illustrate that c.109A> T mutation causes a change in the secondary structure of the protein.Conclusions: Since this heterozygous mutation of the NKX2.6 gene have been observed in conserved region and not detected in any control subjects, and according to the results obtained from bioinformatics, it is expected to affect protein function.
Keywords:NKX2.6, Pymol, Polyphen-2, Psipred, mutation
COI code: IPMCMED03_067
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Ghazi, Donya; Mehri Khatami & Mohammad Mehdi Heidari, 2018, The identification of Mutations in exon1 of NKX2.6 gene in patients with Congenital Heart Defects, Third International Private Medical Congress of Iran, تهران, دانشگاه علوم پزشكي بقيه الله(عج), https://www.civilica.com/Paper-IPMCMED03-IPMCMED03_067.htmlInside the text, wherever referred to or an achievement of this article is mentioned, after mentioning the article, inside the parental, the following specifications are written.
First Time: (Ghazi, Donya; Mehri Khatami & Mohammad Mehdi Heidari, 2018)
Second and more: (Ghazi; Khatami & Heidari, 2018)
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Type: state university
Paper No.: 11280
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