• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

酵母FRE基因在转基因烟草中的表达。

Expression of the yeast FRE genes in transgenic tobacco.

作者信息

Samuelsen A I, Martin R C, Mok D W, Mok M C

机构信息

Department of Horticulture and Center for Gene Research and Biotechnology, Oregon State University, Corvallis, Oregon 97331-7304, USA.

出版信息

Plant Physiol. 1998 Sep;118(1):51-8. doi: 10.1104/pp.118.1.51.

DOI:10.1104/pp.118.1.51
PMID:9733525
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC34873/
Abstract

Two yeast genes, FRE1 and FRE2 (encoding Fe(III) reductases) were placed under the control of the cauliflower mosaic virus 35S promoter and introduced into tobacco (Nicotiana tabacum L.) via Agrobacterium tumefaciens-mediated transformation. Homozygous lines containing FRE1, FRE2, or FRE1 plus FRE2 were generated. Northern-blot analyses revealed mRNA of two different sizes in FRE1 lines, whereas all FRE2 lines had mRNA only of the expected length. Fe(III) reduction, chlorophyll contents, and Fe levels were determined in transgenic and control plants under Fe-sufficient and Fe-deficient conditions. In a normal growth environment, the highest root Fe(III) reduction, 4-fold higher than in controls, occurred in the double transformant (FRE1 + FRE2). Elevated Fe(III) reduction was also observed in all FRE2 and some FRE1 lines. The increased Fe(III) reduction occurred along the entire length of the roots and on shoot sections. FRE2 and double transformants were more tolerant to Fe deficiency in hydroponic culture, as shown by higher chlorophyll and Fe concentrations in younger leaves, whereas FRE1 transformants did not differ from the controls. Overall, the beneficial effects of FRE2 were consistent, suggesting that FRE2 may be used to improve Fe efficiency in crop plants.

摘要

将两个酵母基因FRE1和FRE2(编码铁(III)还原酶)置于花椰菜花叶病毒35S启动子的控制之下,并通过根癌农杆菌介导的转化导入烟草(Nicotiana tabacum L.)。产生了含有FRE1、FRE2或FRE1加FRE2的纯合株系。Northern杂交分析显示,FRE1株系中有两种不同大小的mRNA,而所有FRE2株系仅具有预期长度的mRNA。在铁充足和铁缺乏条件下,测定了转基因植物和对照植物中的铁(III)还原、叶绿素含量和铁水平。在正常生长环境中,双转化体(FRE1 + FRE2)的根中铁(III)还原最高,比对照高4倍。在所有FRE2和一些FRE1株系中也观察到铁(III)还原升高。铁(III)还原增加发生在根的整个长度和茎段上。FRE2和双转化体在水培中对缺铁更耐受,幼叶中的叶绿素和铁浓度更高表明了这一点,而FRE1转化体与对照没有差异。总体而言,FRE2的有益作用是一致的,表明FRE2可用于提高作物植物的铁效率。

相似文献

1
Expression of the yeast FRE genes in transgenic tobacco.酵母FRE基因在转基因烟草中的表达。
Plant Physiol. 1998 Sep;118(1):51-8. doi: 10.1104/pp.118.1.51.
2
Metalloregulation of FRE1 and FRE2 homologs in Saccharomyces cerevisiae.酿酒酵母中FRE1和FRE2同源物的金属调控
J Biol Chem. 1998 Sep 11;273(37):23716-21. doi: 10.1074/jbc.273.37.23716.
3
Regulated expression of the Saccharomyces cerevisiae Fre1p/Fre2p Fe/Cu reductase related genes.酿酒酵母Fre1p/Fre2p铁/铜还原酶相关基因的调控表达。
Yeast. 1999 May;15(7):573-84. doi: 10.1002/(SICI)1097-0061(199905)15:7<573::AID-YEA404>3.0.CO;2-7.
4
The AFT1 transcriptional factor is differentially required for expression of high-affinity iron uptake genes in Saccharomyces cerevisiae.AFT1转录因子对于酿酒酵母中高亲和力铁摄取基因的表达有不同的需求。
Yeast. 1997 Jun 15;13(7):621-37. doi: 10.1002/(SICI)1097-0061(19970615)13:7<621::AID-YEA121>3.0.CO;2-U.
5
Nonsense-mediated mRNA decay of the ferric and cupric reductase mRNAs FRE1 and FRE2 in Saccharomyces cerevisiae.酵母中 ferric 和 cupric reductase mRNAs FRE1 和 FRE2 的无意义介导的 mRNA 衰变。
FEBS Lett. 2019 Nov;593(22):3228-3238. doi: 10.1002/1873-3468.13545. Epub 2019 Jul 30.
6
Cytochrome P-450 reductase is responsible for the ferrireductase activity associated with isolated plasma membranes of Saccharomyces cerevisiae.细胞色素P-450还原酶负责与酿酒酵母分离的质膜相关的铁还原酶活性。
FEMS Microbiol Lett. 1997 Nov 1;156(1):147-52. doi: 10.1111/j.1574-6968.1997.tb12720.x.
7
Ferric reductase of Saccharomyces cerevisiae: molecular characterization, role in iron uptake, and transcriptional control by iron.酿酒酵母的铁还原酶:分子特征、在铁摄取中的作用以及铁对其转录的调控
Proc Natl Acad Sci U S A. 1992 May 1;89(9):3869-73. doi: 10.1073/pnas.89.9.3869.
8
Two distinctly regulated genes are required for ferric reduction, the first step of iron uptake in Saccharomyces cerevisiae.在酿酒酵母中,铁摄取的第一步即铁还原需要两个调控方式截然不同的基因。
Mol Cell Biol. 1994 May;14(5):3065-73. doi: 10.1128/mcb.14.5.3065-3073.1994.
9
AFT1: a mediator of iron regulated transcriptional control in Saccharomyces cerevisiae.AFT1:酿酒酵母中铁调节转录控制的一种介导因子。
EMBO J. 1995 Mar 15;14(6):1231-9. doi: 10.1002/j.1460-2075.1995.tb07106.x.
10
Evidence for Cu(II) reduction as a component of copper uptake by Saccharomyces cerevisiae.铜(II)还原作为酿酒酵母摄取铜的一个组成部分的证据。
J Biol Chem. 1995 Jan 6;270(1):128-34. doi: 10.1074/jbc.270.1.128.

引用本文的文献

1
Genome-wide association studies identifies seven major regions responsible for iron deficiency chlorosis in soybean (Glycine max).全基因组关联研究确定了大豆缺铁黄化的七个主要区域。
PLoS One. 2014 Sep 16;9(9):e107469. doi: 10.1371/journal.pone.0107469. eCollection 2014.
2
Differential gene expression analysis provides new insights into the molecular basis of iron deficiency stress response in the citrus rootstock Poncirus trifoliata (L.) Raf.差异基因表达分析为研究枳砧铁亏缺胁迫响应的分子基础提供了新的见解。
J Exp Bot. 2010;61(2):483-90. doi: 10.1093/jxb/erp328. Epub 2009 Nov 13.
3
Iron deficiency in pregnancy and the rationality of iron supplements prescribed during pregnancy.孕期缺铁及孕期补铁处方的合理性。
Medscape J Med. 2008;10(12):283. Epub 2008 Dec 16.
4
Molecular and phenotypic characterization of transgenic soybean expressing the Arabidopsis ferric chelate reductase gene, FRO2.表达拟南芥铁螯合还原酶基因FRO2的转基因大豆的分子与表型特征分析
Planta. 2006 Oct;224(5):1116-28. doi: 10.1007/s00425-006-0293-1. Epub 2006 Jun 2.
5
Phytoremediation of toxic trace elements in soil and water.土壤和水中有毒微量元素的植物修复
J Ind Microbiol Biotechnol. 2005 Dec;32(11-12):514-20. doi: 10.1007/s10295-005-0227-0. Epub 2005 May 10.

本文引用的文献

1
Mechanism of iron uptake by peanut plants : I. Fe reduction, chelate splitting, and release of phenolics.花生植株吸收铁的机制:I. 铁还原、螯合物分解及酚类物质的释放
Plant Physiol. 1983 Apr;71(4):949-54. doi: 10.1104/pp.71.4.949.
2
Iron: Nutritious, Noxious, and Not Readily Available.铁:营养丰富、有害且难以获取。
Plant Physiol. 1994 Mar;104(3):815-820. doi: 10.1104/pp.104.3.815.
3
Shoot-to-Root Signal Transmission Regulates Root Fe(III) Reductase Activity in the dgl Mutant of Pea.地上部到根部的信号传递调控豌豆dgl突变体中根铁(III)还原酶活性
Plant Physiol. 1996 Jan;110(1):329-334. doi: 10.1104/pp.110.1.329.
4
The FRE1 ferric reductase of Saccharomyces cerevisiae is a cytochrome b similar to that of NADPH oxidase.酿酒酵母的FRE1铁还原酶是一种与NADPH氧化酶相似的细胞色素b。
J Biol Chem. 1996 Jun 14;271(24):14240-4. doi: 10.1074/jbc.271.24.14240.
5
Evidence for the Saccharomyces cerevisiae ferrireductase system being a multicomponent electron transport chain.酿酒酵母铁还原酶系统作为多组分电子传递链的证据。
J Biol Chem. 1996 Jun 7;271(23):13578-83. doi: 10.1074/jbc.271.23.13578.
6
The fission yeast ferric reductase gene frp1+ is required for ferric iron uptake and encodes a protein that is homologous to the gp91-phox subunit of the human NADPH phagocyte oxidoreductase.裂殖酵母铁还原酶基因frp1+是摄取三价铁所必需的,它编码一种与人类NADPH吞噬细胞氧化还原酶的gp91-phox亚基同源的蛋白质。
Mol Cell Biol. 1993 Jul;13(7):4342-50. doi: 10.1128/mcb.13.7.4342-4350.1993.
7
Two distinctly regulated genes are required for ferric reduction, the first step of iron uptake in Saccharomyces cerevisiae.在酿酒酵母中,铁摄取的第一步即铁还原需要两个调控方式截然不同的基因。
Mol Cell Biol. 1994 May;14(5):3065-73. doi: 10.1128/mcb.14.5.3065-3073.1994.
8
Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes.点突变确定了AUG起始密码子侧翼的一个序列,该序列可调节真核生物核糖体的翻译。
Cell. 1986 Jan 31;44(2):283-92. doi: 10.1016/0092-8674(86)90762-2.
9
Vectors for cell-free expression and mutagenesis of protein-coding sequences.用于无细胞表达和蛋白质编码序列诱变的载体。
Nucleic Acids Res. 1987 Dec 10;15(23):10066. doi: 10.1093/nar/15.23.10066.
10
Iron uptake by the yeast Saccharomyces cerevisiae: involvement of a reduction step.酿酒酵母对铁的摄取:还原步骤的参与
J Gen Microbiol. 1987 Nov;133(11):3229-36. doi: 10.1099/00221287-133-11-3229.