glr-3基因功能及其同源蛋白的聚类与分化

Yue Ma, Tiantian Guo, Yihe Wang, Xinna Li, Jingyu Zhang
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引用次数: 0

摘要

生物为了适应低温环境,通过热感系统将兴奋传递给中枢系统,这是一种经典的反射反应。冷受体GLR-3通过外周感觉神经元ASER感知冷并产生冷回避行为。为了进一步了解冷感glr-3基因的基因编码及其同源基因群功能和蛋白功能的进化,我们获得了24个物种glr-3基因及其同源基因的核苷酸序列和氨基酸序列并进行了比较。通过与中国林蛙GRIK2基因序列聚类,采用生物信息学方法对其基因变化、进化速率、蛋白质理化性质、糖基化位点、磷酸化位点、蛋白质二级结构和三级结构进行预测和测序分析。分析结果表明,glr-3基因及其同源基因具有明显的正向选择效应。蛋白质预测分析表明,这25种植物的glr-3基因及其同源基因编码的蛋白质均为亲水性蛋白,且脂肪族氨基酸侧链比例较高。跨膜螺旋分布广泛,n -糖基化位点和o -糖基化位点较多。编码的蛋白磷酸化位点为丝氨酸、苏氨酸和酪氨酸磷酸化位点。二级结构预测表明,编码蛋白的二级结构单元为α-螺旋、β-转、随机螺旋和延伸链,其中α-螺旋所占比例最大。本研究为寒感基因glr-3及其同源基因的进化和功能提供了有益的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clustering and Differentiation of glr-3 Gene Function and Its Homologous Proteins
In order to adapt to the low temperature environment, organisms transmitexcitement to the central system through the thermal sensing system, whichis a classic reflex reaction. The cold receptor GLR-3 perceives cold and produces cold avoidance behavior through peripheral sensory neurons ASER.In order to further understand the gene encoding of the cold sensing glr-3gene and the evolution of its homologous gene group function and proteinfunction, the nucleotide sequence and amino acid sequence of the glr-3gene and its homologous gene in 24 species were obtained and compared.By clustering with the GRIK2 gene sequence of Rana chensinensis, the bioinformatics method was used to predict and sequence analyze the change ofgene, evolution rate, physical and chemical properties of protein, glycosylation sites, phosphorylation sites, secondary structure and tertiary structureof protein. The analysis results show that the glr-3 gene and its homologousgene have obvious positive selection effect. The protein prediction analysisshowed that the glr-3 gene and its homologous genes encoded proteinsin these 25 species were hydrophilic proteins, and the proportion of sidechains of aliphatic amino acids was high. The transmembrane helix waswidespread and there were more N-glycosylation sites and O-glycosylationsites. The protein phosphorylation sites encoded were serine, threonine andtyrosine phosphorylation sites. Secondary structure prediction showed thatthe secondary structure units of the encoded protein were α-helix, β-turn,random coil and extended chain, and the proportion of α-helix was the largest. This study provides useful information on the evolution and function ofthe cold sensing gene glr-3 and its homologous genes.
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