从液泡gs-x泵到多特异性ABC转运体。

Philip A. Rea, Ze-Sheng Li, Yu-Ping Lu, Yolanda M. Drozdowicz, Enrico Martinoia
{"title":"从液泡gs-x泵到多特异性ABC转运体。","authors":"Philip A. Rea,&nbsp;Ze-Sheng Li,&nbsp;Yu-Ping Lu,&nbsp;Yolanda M. Drozdowicz,&nbsp;Enrico Martinoia","doi":"10.1146/annurev.arplant.49.1.727","DOIUrl":null,"url":null,"abstract":"<p><p>While the concept of H+-coupling has dominated studies of energy-dependent organic solute transport in plants for over two decades, recent studies have demonstrated the existence of a group of organic solute transporters, belonging to the ATP-binding cassette (ABC) superfamily, that are directly energized by MgATP rather than by a transmembrane H+-electrochemical potential difference. Originally identified in microbial and animal cells, the ABC superfamily is one of the largest and most widespread protein families known. Competent in the transport of a broad range of substances including sugars, peptides, alkaloids, inorganic anions, and lipids, all ABC transporters are constituted of one or two copies each of an integral membrane sector and cytosolically oriented ATP-binding domain. To date, two major subclasses, the multidrug resistance-associated proteins (MRPs) and multidrug resistance proteins (MDRs) (so named because of the phenotypes conferred by their animal prototypes), have been identified molecularly in plants. However, only the MRPs have been defined functionally. This review therefore focuses on the functional capabilities, energetics, organization, and regulation of the plant MRPs. Otherwise known as GS-X pumps, or glutathione-conjugate or multispecific organic anion Mg2+-ATPases, the MRPs are considered to participate in the transport of exogenous and endogenous amphipathic anions and glutathionated compounds from the cytosol into the vacuole. Encoded by a multigene family and possessing a unique domain organization, the types of processes that likely converge and depend on plant MRPs include herbicide detoxification, cell pigmentation, the alleviation of oxidative damage, and the storage of antimicrobial compounds. Additional functional capabilities might include channel regulation or activity, and/or the transport of heavy metal chelates. The identification of the MRPs, in particular, and the demonstration of a central role for ABC transporters, in general, in plant function not only provide fresh insights into the molecular basis of energy-dependent solute transport but also offer the prospect for manipulating and investigating many fundamental processes that have hitherto evaded analysis at the transport level.</p>","PeriodicalId":80493,"journal":{"name":"Annual review of plant physiology and plant molecular biology","volume":"49 ","pages":"727-760"},"PeriodicalIF":0.0000,"publicationDate":"1998-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1146/annurev.arplant.49.1.727","citationCount":"320","resultStr":"{\"title\":\"FROM VACUOLAR GS-X PUMPS TO MULTISPECIFIC ABC TRANSPORTERS.\",\"authors\":\"Philip A. Rea,&nbsp;Ze-Sheng Li,&nbsp;Yu-Ping Lu,&nbsp;Yolanda M. Drozdowicz,&nbsp;Enrico Martinoia\",\"doi\":\"10.1146/annurev.arplant.49.1.727\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>While the concept of H+-coupling has dominated studies of energy-dependent organic solute transport in plants for over two decades, recent studies have demonstrated the existence of a group of organic solute transporters, belonging to the ATP-binding cassette (ABC) superfamily, that are directly energized by MgATP rather than by a transmembrane H+-electrochemical potential difference. Originally identified in microbial and animal cells, the ABC superfamily is one of the largest and most widespread protein families known. Competent in the transport of a broad range of substances including sugars, peptides, alkaloids, inorganic anions, and lipids, all ABC transporters are constituted of one or two copies each of an integral membrane sector and cytosolically oriented ATP-binding domain. To date, two major subclasses, the multidrug resistance-associated proteins (MRPs) and multidrug resistance proteins (MDRs) (so named because of the phenotypes conferred by their animal prototypes), have been identified molecularly in plants. However, only the MRPs have been defined functionally. This review therefore focuses on the functional capabilities, energetics, organization, and regulation of the plant MRPs. Otherwise known as GS-X pumps, or glutathione-conjugate or multispecific organic anion Mg2+-ATPases, the MRPs are considered to participate in the transport of exogenous and endogenous amphipathic anions and glutathionated compounds from the cytosol into the vacuole. Encoded by a multigene family and possessing a unique domain organization, the types of processes that likely converge and depend on plant MRPs include herbicide detoxification, cell pigmentation, the alleviation of oxidative damage, and the storage of antimicrobial compounds. Additional functional capabilities might include channel regulation or activity, and/or the transport of heavy metal chelates. The identification of the MRPs, in particular, and the demonstration of a central role for ABC transporters, in general, in plant function not only provide fresh insights into the molecular basis of energy-dependent solute transport but also offer the prospect for manipulating and investigating many fundamental processes that have hitherto evaded analysis at the transport level.</p>\",\"PeriodicalId\":80493,\"journal\":{\"name\":\"Annual review of plant physiology and plant molecular biology\",\"volume\":\"49 \",\"pages\":\"727-760\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1998-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1146/annurev.arplant.49.1.727\",\"citationCount\":\"320\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annual review of plant physiology and plant molecular biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1146/annurev.arplant.49.1.727\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annual review of plant physiology and plant molecular biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1146/annurev.arplant.49.1.727","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 320

摘要

虽然氢离子偶联的概念已经主导了植物中能量依赖性有机溶质运输的研究超过二十年,但最近的研究表明,存在一组有机溶质转运体,属于atp结合盒(ABC)超家族,它们直接由MgATP而不是通过跨膜H+电化学电位差供电。最初在微生物和动物细胞中发现,ABC超家族是已知的最大和最广泛的蛋白质家族之一。所有ABC转运蛋白都能运输多种物质,包括糖、多肽、生物碱、无机阴离子和脂质,它们由一个或两个完整的膜区和细胞质导向的atp结合域组成。迄今为止,已经在植物分子中确定了两个主要亚类,即多药耐药相关蛋白(MRPs)和多药耐药蛋白(mdr)(因其动物原型所赋予的表型而得名)。然而,只有mrp在功能上被定义。本文就植物MRPs的功能、能量学、组织和调控等方面进行综述。也被称为GS-X泵,或谷胱甘肽偶联或多特异性有机阴离子Mg2+- atp酶,MRPs被认为参与外源性和内源性两亲性阴离子和谷胱甘肽化合物从细胞质转运到液泡。MRPs由一个多基因家族编码,具有独特的结构域组织,可能集中并依赖于植物MRPs的过程类型包括除草剂解毒、细胞色素沉着、氧化损伤减轻和抗菌化合物的储存。其他功能可能包括通道调节或活性,和/或重金属螯合物的运输。特别是mrp的鉴定,以及ABC转运蛋白在植物功能中的核心作用的证明,不仅为能量依赖的溶质运输的分子基础提供了新的见解,而且为操纵和研究迄今为止在运输水平上逃避分析的许多基本过程提供了前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
FROM VACUOLAR GS-X PUMPS TO MULTISPECIFIC ABC TRANSPORTERS.

While the concept of H+-coupling has dominated studies of energy-dependent organic solute transport in plants for over two decades, recent studies have demonstrated the existence of a group of organic solute transporters, belonging to the ATP-binding cassette (ABC) superfamily, that are directly energized by MgATP rather than by a transmembrane H+-electrochemical potential difference. Originally identified in microbial and animal cells, the ABC superfamily is one of the largest and most widespread protein families known. Competent in the transport of a broad range of substances including sugars, peptides, alkaloids, inorganic anions, and lipids, all ABC transporters are constituted of one or two copies each of an integral membrane sector and cytosolically oriented ATP-binding domain. To date, two major subclasses, the multidrug resistance-associated proteins (MRPs) and multidrug resistance proteins (MDRs) (so named because of the phenotypes conferred by their animal prototypes), have been identified molecularly in plants. However, only the MRPs have been defined functionally. This review therefore focuses on the functional capabilities, energetics, organization, and regulation of the plant MRPs. Otherwise known as GS-X pumps, or glutathione-conjugate or multispecific organic anion Mg2+-ATPases, the MRPs are considered to participate in the transport of exogenous and endogenous amphipathic anions and glutathionated compounds from the cytosol into the vacuole. Encoded by a multigene family and possessing a unique domain organization, the types of processes that likely converge and depend on plant MRPs include herbicide detoxification, cell pigmentation, the alleviation of oxidative damage, and the storage of antimicrobial compounds. Additional functional capabilities might include channel regulation or activity, and/or the transport of heavy metal chelates. The identification of the MRPs, in particular, and the demonstration of a central role for ABC transporters, in general, in plant function not only provide fresh insights into the molecular basis of energy-dependent solute transport but also offer the prospect for manipulating and investigating many fundamental processes that have hitherto evaded analysis at the transport level.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信