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人类 Bcl2 相关抗凋亡基因-1(BAG-1)的起源与进化。

Origin and Evolution of the Human Bcl2-Associated Athanogene-1 (BAG-1).

机构信息

Department of Biological Science, Center for Applied Biotechnology Studies, and Center for Computational and Applied Mathematics, College of Natural Sciences and Mathematics, California State University Fullerton, Fullerton, CA 92834-6850, USA.

Department of Genome Sciences, Molecular and Cellular Biology Graduate Program, University of Washington, Seattle, WA 98195, USA.

出版信息

Int J Mol Sci. 2020 Dec 18;21(24):9701. doi: 10.3390/ijms21249701.

Abstract

Molecular chaperones, particularly the 70-kDa heat shock proteins (Hsp70s), are key orchestrators of the cellular stress response. To perform their critical functions, Hsp70s require the presence of specific co-chaperones, which include nucleotide exchange factors containing the BCL2-associated athanogene (BAG) domain. BAG-1 is one of these proteins that function in a wide range of cellular processes, including apoptosis, protein refolding, and degradation, as well as tumorigenesis. However, the origin of BAG-1 proteins and their evolution between and within species are mostly uncharacterized. This report investigated the macro- and micro-evolution of BAG-1 using orthologous sequences and single nucleotide polymorphisms (SNPs) to elucidate the evolution and understand how natural variation affects the cellular stress response. We first collected and analyzed several BAG-1 sequences across animals, plants, and fungi; mapped intron positions and phases; reconstructed phylogeny; and analyzed protein characteristics. These data indicated that BAG-1 originated before the animals, plants, and fungi split, yet most extant fungal species have lost BAG-1. Furthermore, although BAG-1's structure has remained relatively conserved, kingdom-specific conserved differences exist at sites of known function, suggesting functional specialization within each kingdom. We then analyzed SNPs from the 1000 genomes database to determine the evolutionary patterns within humans. These analyses revealed that the SNP density is unequally distributed within the gene, and the ratio of non-synonymous/synonymous SNPs is significantly higher than 1 in the BAG domain region, which is an indication of positive selection. To further explore this notion, we performed several biochemical assays and found that only one out of five mutations tested altered the major co-chaperone properties of BAG-1. These data collectively suggest that although the co-chaperone functions of BAG-1 are highly conserved and can probably tolerate several radical mutations, BAG-1 might have acquired specialized and potentially unexplored functions during the evolutionary process.

摘要

分子伴侣,特别是 70kDa 热休克蛋白(Hsp70s),是细胞应激反应的关键协调者。为了发挥其关键功能,Hsp70s 需要特定的共伴侣存在,其中包括含有 BCL2 相关抗凋亡基因(BAG)结构域的核苷酸交换因子。BAG-1 是这些蛋白质之一,在多种细胞过程中发挥作用,包括细胞凋亡、蛋白质重折叠和降解以及肿瘤发生。然而,BAG-1 蛋白的起源及其在物种之间和内部的进化大多尚未确定。本报告使用同源序列和单核苷酸多态性(SNP)研究了 BAG-1 的宏观和微观进化,以阐明进化并了解自然变异如何影响细胞应激反应。我们首先收集并分析了动物、植物和真菌中的几个 BAG-1 序列;映射了内含子位置和相位;重建了系统发育;并分析了蛋白质特征。这些数据表明,BAG-1 起源于动物、植物和真菌分化之前,但大多数现存的真菌物种已经失去了 BAG-1。此外,尽管 BAG-1 的结构相对保守,但在已知功能的位点存在特定于王国的保守差异,表明每个王国都有功能专业化。然后,我们分析了来自 1000 基因组数据库的 SNP,以确定人类内部的进化模式。这些分析表明,SNP 密度在基因内不均匀分布,BAG 结构域区域的非同义/同义 SNP 比值明显高于 1,这表明存在正选择。为了进一步探讨这一观点,我们进行了几项生化测定,发现只有五个测试突变中的一个改变了 BAG-1 的主要共伴侣特性。这些数据共同表明,尽管 BAG-1 的共伴侣功能高度保守,可能可以耐受几种激进突变,但 BAG-1 在进化过程中可能获得了专门的、可能尚未被探索的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2f0/7766421/78b475864396/ijms-21-09701-g001.jpg

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