Jamshidi Kandjani Omid, Rahbar-Shahrouziasl Mahdieh, Alizadeh Ali Akbar, Hamzeh-Mivehroud Maryam, Dastmalchi Siavoush
Biotechnology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
School of Pharmacy, Tabriz University of Medical Sciences, Tabriz, Iran.
Adv Pharm Bull. 2021 May;11(3):557-563. doi: 10.34172/apb.2021.064. Epub 2020 May 9.
DOF (DNA-binding with One Finger) proteins are plant-specific transcription factors which mediate numerous biological processes. The purpose of the current study is to report new naturally occurring mutations in the gene encoding for one of the members of DOF proteins named DOF 4.2. The expression of zinc finger domain of DOF 4.2 (DOF 4.2-ZF) was investigated by first synthesis of cDNA library using different parts of plant. Then the coding sequence for zinc finger domain of DOF 4.2 protein was prepared using nested PCR experiment and cloned into pGEX-6P-1 expression vector. Finally, the prepared construct was used for protein expression. Furthermore, molecular dynamics (MD) simulation was carried out to predict DNA binding affinity of DOF 4.2-ZF using AMBER package. For the first time a new variant of DOF 4.2-ZF protein with three mutations was detected. One of the mutations is silent while the other two mutations lead to amino acid replacement (S18G) as well as introduction of a stop codon ultimately resulting in a truncated protein production. In order to investigate whether the truncated form is able to recognize DNA binding motif, MD simulations were carried out and the results showed that the chance of binding of DOF 4.2-ZF protein to cognate DNA in its truncated form is very low. The findings demonstrated that the observed mutations adversely affect the DNA binding ability of the truncated form of DOF4.2 if it is expressed in the mutant variant of used in this study.
单指DNA结合(DOF)蛋白是植物特有的转录因子,介导众多生物学过程。本研究的目的是报告在编码DOF蛋白成员之一DOF 4.2的基因中自然发生的新突变。通过首先使用植物的不同部位合成cDNA文库来研究DOF 4.2的锌指结构域(DOF 4.2-ZF)的表达。然后使用巢式PCR实验制备DOF 4.2蛋白锌指结构域的编码序列,并克隆到pGEX-6P-1表达载体中。最后,将制备的构建体用于蛋白质表达。此外,使用AMBER软件包进行分子动力学(MD)模拟,以预测DOF 4.2-ZF与DNA的结合亲和力。首次检测到具有三个突变的DOF 4.2-ZF蛋白的新变体。其中一个突变是沉默突变,而其他两个突变导致氨基酸替换(S18G)以及引入终止密码子,最终导致截短蛋白的产生。为了研究截短形式是否能够识别DNA结合基序,进行了MD模拟,结果表明截短形式的DOF 4.2-ZF蛋白与同源DNA结合的机会非常低。研究结果表明,如果在本研究中使用的突变变体中表达,观察到的突变会对截短形式的DOF4.2的DNA结合能力产生不利影响。