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大规模鉴定、计算机模拟分析及小麦 SNARE 和 NPSN 基因家族在囊泡运输中的互作研究。

Genome-Scale Identification, in Silico Characterization and Interaction Study Between Wheat SNARE and NPSN Gene Families Involved in Vesicular Transport.

出版信息

IEEE/ACM Trans Comput Biol Bioinform. 2021 Nov-Dec;18(6):2492-2501. doi: 10.1109/TCBB.2020.2981896. Epub 2021 Dec 8.

Abstract

Wheat is an important cereal crop grown worldwide but it's yield is severely affected by various biotic and abiotic stresses. SNAREs are key regulators of vesicle trafficking and are present in abundance in higher plant species suggesting their prominence in growth and development. Novel Plant SNAREs (NPSN) are found exclusively in plants. Hence, a comprehensive analysis of these two gene families in wheat genome was accomplished in this study. We report here 27 SNAREs and eight NPSN genes. These genes and their respective proteins were investigated for gene structure, physiochemical properties, domain and motif architecture, phylogeny, chromosomal localization and possible interactions. Phylogenetic and motif analysis confirmed SNARE domain in all the proteins. Functional annotation revealed participation in biological process like vesicle fusion, exocytosis, protein targeting to vacuole and SNAP receptor activity. At subcellular level, SNAREs were localized in multiple organelles whereas NPSN proteins were localized in cytoplasm where they regulate vesicle fusion. The 3-D structures built with Modeller proved the presence of SNARE motifs in the identified proteins. Possible protein-protein interactions between SNARE and NPSN proteins were determined and docking was performed. The results augmented our understanding about molecular function, evolutionary relation, location inside the cell and their interactions.

摘要

小麦是全球广泛种植的重要粮食作物,但它的产量受到各种生物和非生物胁迫的严重影响。SNAREs 是囊泡运输的关键调节剂,在高等植物物种中大量存在,表明它们在生长和发育中具有重要作用。新型植物 SNAREs(NPSN)仅存在于植物中。因此,本研究对小麦基因组中的这两个基因家族进行了全面分析。我们在此报告了 27 个 SNAREs 和 8 个 NPSN 基因。这些基因及其相应的蛋白质在基因结构、理化性质、结构域和基序结构、系统发育、染色体定位和可能的相互作用方面进行了研究。系统发育和基序分析证实了所有蛋白质中的 SNARE 结构域。功能注释表明它们参与了生物过程,如囊泡融合、胞吐作用、蛋白靶向液泡和 SNAP 受体活性。在亚细胞水平上,SNAREs 定位于多种细胞器,而 NPSN 蛋白定位于细胞质,在细胞质中它们调节囊泡融合。使用 Modeller 构建的 3-D 结构证明了鉴定出的蛋白质中存在 SNARE 基序。确定了 SNARE 和 NPSN 蛋白之间可能的蛋白质-蛋白质相互作用,并进行了对接。结果增强了我们对分子功能、进化关系、细胞内位置及其相互作用的理解。

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