Suppr超能文献

一种化学排斥受体基因敲除突变的行为学效应 于……

Behavioral Effects of a Chemorepellent Receptor Knockout Mutation in .

作者信息

Zou Dianxiong, Hennessey Todd M

机构信息

Department of Biological Sciences, University at Buffalo, Amherst, New York, USA.

出版信息

mSphere. 2017 Jul 5;2(4). doi: 10.1128/mSphere.00182-17. eCollection 2017 Jul-Aug.

Abstract

A conditioned supernatant from contains a powerful chemorepellent for wild-type cells, and a gene called is required for this response. This is the first genomic identification of a chemorepellent receptor in any eukaryotic unicellular organism. This conditioned supernatant factor (CSF) is small (<1 kDa), and its repellent effect is resistant to boiling, protease treatment, and nuclease digestion. External BAPTA eliminated the CSF response, suggesting that Ca entry is required for the classical avoiding reactions (AR) used for chemorepulsion. A macronuclear gene knockout (G37-KO) mutant is both nonresponsive to the CSF and overresponsive to other repellents such as quinine, lysozyme, GTP, and high potassium concentrations. All of these mutant phenotypes were reversed by overexpression of the wild-type gene in a overexpression mutant. Overexpression of in the wild type caused increased responsiveness to the CSF and underresponsiveness to high K concentrations. Behavioral adaptation (by prolonged exposure to the CSF) caused decreases in responsiveness to all of the stimuli used in the wild type and the overexpression mutant but not in the G37-KO mutant. We propose that the constant presence of the CSF causes a decreased basal excitability of the wild type due to chemosensory adaptation through and that all of the G37-KO phenotypes are due to an inability to detect the CSF. Therefore, the G37 protein may be the CSF receptor. The physiological role of these G37-mediated responses may be to both moderate basal excitability and detect the CSF as an indicator of high cell density growth. Although many single-cell eukaryotes have served as classical model systems for chemosensory studies for decades, the major emphasis has been on chemoattraction and no chemorepellent receptor gene has been identified in any unicellular eukaryote. This is the first description of a gene that codes for a chemorepellent receptor in any protozoan. Integration of both depolarizing chemorepellent pathways and hyperpolarizing chemoattractant pathways is as important to chemoresponses of motile unicells as excitatory and inhibitory neurotransmitter pathways are to neurons. Therefore, both chemoattractant and chemorepellent pathways should be represented in a useful unicellular model system. cells provide such a model system because simple behavioral bioassays, gene knockouts, biochemical analysis, and other approaches can be used with these eukaryotic model cells. This work can contribute to the basic understanding of unicellular sensory responses and provide insights into the evolution of chemoreceptors and possible chemorepellent approaches for preventing infections by some pathogenic protozoa.

摘要

来自[具体来源未提及]的条件培养基上清液含有一种对野生型细胞具有强大化学排斥作用的物质,并且一种名为[具体基因未提及]的基因参与了这一反应。这是在任何真核单细胞生物中首次对化学排斥受体进行的基因组鉴定。这种条件培养基上清液因子(CSF)很小(<1 kDa),其排斥作用对煮沸、蛋白酶处理和核酸酶消化具有抗性。细胞外BAPTA消除了CSF反应,表明钙离子内流是化学排斥所使用的经典回避反应(AR)所必需的。一个大核[具体基因未提及]基因敲除(G37-KO)突变体对CSF无反应,而对其他排斥剂如奎宁、溶菌酶、GTP和高钾浓度反应过度。在一个[具体基因未提及]过表达突变体中,野生型[具体基因未提及]基因的过表达逆转了所有这些突变表型。在野生型中过表达[具体基因未提及]导致对CSF的反应性增加,而对高钾浓度的反应性降低。行为适应(通过长时间暴露于CSF)导致野生型和过表达突变体中对所有使用的刺激的反应性降低,但G37-KO突变体中没有。我们提出,CSF的持续存在由于通过[具体基因未提及]的化学感觉适应而导致野生型的基础兴奋性降低,并且所有G37-KO表型是由于无法检测到CSF。因此,G37蛋白可能是CSF受体。这些由G37介导的反应的生理作用可能是调节基础兴奋性并检测CSF作为高细胞密度生长的指标。尽管几十年来许多单细胞真核生物一直作为化学感觉研究的经典模型系统,但主要重点一直是化学吸引,并且在任何单细胞真核生物中都未鉴定出化学排斥受体基因。这是首次描述在任何原生动物中编码化学排斥受体的基因。去极化化学排斥途径和超极化化学吸引途径两者的整合对于运动单细胞的化学反应与兴奋性和抑制性神经递质途径对于神经元一样重要。因此,化学吸引和化学排斥途径都应在一个有用的单细胞模型系统中有所体现。[具体细胞名称未提及]细胞提供了这样一个模型系统,因为可以对这些真核模型细胞使用简单的行为生物测定、基因敲除、生化分析和其他方法。这项工作有助于对单细胞感觉反应的基本理解,并为化学感受器的进化以及预防某些致病原生动物感染的可能化学排斥方法提供见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f2/5497023/87327409af3a/sph0041723160001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验