• 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

转基因水稻植株中水稻Act1基因5'区域活性分析

Analysis of rice Act1 5' region activity in transgenic rice plants.

作者信息

Zhang W, McElroy D, Wu R

机构信息

Cornell University, Ithaca, New York 14853.

出版信息

Plant Cell. 1991 Nov;3(11):1155-65. doi: 10.1105/tpc.3.11.1155.

DOI:10.1105/tpc.3.11.1155
PMID:1821763
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC160082/
Abstract

The 5' region of the rice actin 1 gene (Act1) has been developed as an efficient regulator of foreign gene expression in transgenic rice plants. To determine the pattern and level of rice Act1 5' region activity, transgenic rice plants containing the Act1 5' region fused to a bacterial beta-glucuronidase (Gus) coding sequence were generated. Two independent clonal lines of transgenic rice plants were analyzed in detail. Quantitative analysis showed that tissue from these transgenic rice plants have a level of GUS protein that represents as much as 3% of total soluble protein. We were able to demonstrate that Act1-Gus gene expression is constitutive throughout the sporophytic and gametophytic tissues of these transgenic rice plants. Plants from one transgenic line were analyzed for the segregation of GUS activity in pollen by in situ histochemical staining, and the inheritance and stability of Act1-Gus expression were assayed in subsequently derived progeny plants.

摘要

水稻肌动蛋白1基因(Act1)的5'区域已被开发为转基因水稻植株中外源基因表达的有效调控元件。为了确定水稻Act1 5'区域活性的模式和水平,构建了含有与细菌β-葡萄糖醛酸酶(Gus)编码序列融合的Act1 5'区域的转基因水稻植株。对两个独立的转基因水稻克隆系进行了详细分析。定量分析表明,这些转基因水稻植株的组织中GUS蛋白水平高达总可溶性蛋白的3%。我们能够证明,Act1-Gus基因在这些转基因水稻植株的孢子体和配子体组织中均组成型表达。通过原位组织化学染色分析了一个转基因系植株花粉中GUS活性的分离情况,并在随后衍生的后代植株中检测了Act1-Gus表达的遗传和稳定性。

相似文献

1
Analysis of rice Act1 5' region activity in transgenic rice plants.转基因水稻植株中水稻Act1基因5'区域活性分析
Plant Cell. 1991 Nov;3(11):1155-65. doi: 10.1105/tpc.3.11.1155.
2
Systemic induction of a potato pin2 promoter by wounding, methyl jasmonate, and abscisic acid in transgenic rice plants.在转基因水稻植株中,创伤、茉莉酸甲酯和脱落酸对马铃薯pin2启动子的系统诱导。
Plant Mol Biol. 1993 Jul;22(4):573-88. doi: 10.1007/BF00047399.
3
Construction of expression vectors based on the rice actin 1 (Act1) 5' region for use in monocot transformation.基于水稻肌动蛋白1(Act1)5'区域构建用于单子叶植物转化的表达载体。
Mol Gen Genet. 1991 Dec;231(1):150-60. doi: 10.1007/BF00293832.
4
Isolation of an efficient actin promoter for use in rice transformation.用于水稻转化的高效肌动蛋白启动子的分离
Plant Cell. 1990 Feb;2(2):163-71. doi: 10.1105/tpc.2.2.163.
5
Characterization of cis-acting elements regulating transcription from the promoter of a constitutively active rice actin gene.调控组成型活性水稻肌动蛋白基因启动子转录的顺式作用元件的表征
Mol Cell Biol. 1992 Aug;12(8):3399-406. doi: 10.1128/mcb.12.8.3399-3406.1992.
6
Identification of a rice actin2 gene regulatory region for high-level expression of transgenes in monocots.单子叶植物中转基因高水平表达的水稻肌动蛋白2基因调控区的鉴定
Plant Biotechnol J. 2009 Apr;7(3):227-39. doi: 10.1111/j.1467-7652.2008.00393.x.
7
[Specific expression of the foreign gene regulated by the rice rbcS promoter in transgenic rice].[水稻rbcS启动子调控外源基因在转基因水稻中的特异性表达]
Zhi Wu Sheng Li Yu Fen Zi Sheng Wu Xue Xue Bao. 2005 Jun;31(3):247-53.
8
[Expression of the GUS fusion gene controlled by the tomato rbcS3A promoter in transgenic rice].[番茄rbcS3A启动子控制的GUS融合基因在转基因水稻中的表达]
Zhi Wu Sheng Li Yu Fen Zi Sheng Wu Xue Xue Bao. 2007 Jun;33(3):251-7.
9
The rice metallothionein gene promoter does not direct foreign gene expression in seed endosperm.水稻金属硫蛋白基因启动子不能指导外源基因在种子胚乳中表达。
Plant Cell Rep. 2004 Oct;23(4):231-5. doi: 10.1007/s00299-004-0813-z. Epub 2004 Jul 20.
10
Expression of the rice Osgrp1 promoter-Gus reporter gene is specifically associated with cell elongation/expansion and differentiation.水稻Osgrp1启动子-Gus报告基因的表达与细胞伸长/扩张及分化特异性相关。
Plant Mol Biol. 1995 Jun;28(3):455-71. doi: 10.1007/BF00020394.

引用本文的文献

1
Varying the expression pattern of the strigolactone receptor gene results in phenotypes distinct from both wild type and knockout mutants.改变独脚金内酯受体基因的表达模式会导致与野生型和基因敲除突变体都不同的表型。
Front Plant Sci. 2023 Oct 11;14:1277617. doi: 10.3389/fpls.2023.1277617. eCollection 2023.
2
Target Lines for Gene Stacking in Rice.水稻基因叠加的目标线。
Int J Mol Sci. 2022 Aug 20;23(16):9385. doi: 10.3390/ijms23169385.
3
Transgenic rice plants expressing the α-L-arabinofuranosidase of exhibit strong dwarfism and markedly enhanced tillering.表达 的α-L-阿拉伯呋喃糖苷酶的转基因水稻植株表现出强烈的矮化和显著增强的分蘖。 (注:原文中“of ”后面内容缺失)
Plant Biotechnol (Tokyo). 2021 Sep 25;38(3):379-386. doi: 10.5511/plantbiotechnology.21.0616a.
4
A 100 bp GAGA motif-containing sequence in AGAMOUS second intron is able to suppress the activity of CaMV35S enhancer in vegetative tissues.AGAMOUS 第二内含子中含有 100 bp GAGA 基序的序列能够抑制 CaMV35S 增强子在营养组织中的活性。
PLoS One. 2020 Mar 5;15(3):e0230203. doi: 10.1371/journal.pone.0230203. eCollection 2020.
5
A Plant-Specific Homolog Influences Gametophyte Development in Sexual Tetraploid Ovules.一种植物特有的同源物影响有性四倍体胚珠中的配子体发育。
Front Plant Sci. 2019 Nov 29;10:1566. doi: 10.3389/fpls.2019.01566. eCollection 2019.
6
A Fruitful Decade Using Synthetic Promoters in the Improvement of Transgenic Plants.利用合成启动子改良转基因植物的丰硕十年。
Front Plant Sci. 2019 Nov 1;10:1433. doi: 10.3389/fpls.2019.01433. eCollection 2019.
7
Development of gene expression system in egg cells and zygotes isolated from rice and maize.从水稻和玉米中分离的卵细胞和受精卵中基因表达系统的开发。
Plant Direct. 2017 Sep 6;1(3):e00010. doi: 10.1002/pld3.10. eCollection 2017 Sep.
8
Evaluation of five promoters for use in transformation of oil palm (Elaeis guineensis Jacq.).用于油棕(Elaeis guineensis Jacq.)转化的五种启动子的评估。
Plant Cell Rep. 1997 Feb;16(5):277-281. doi: 10.1007/BF01088280.
9
The MAP3K-Coding () Gene Is Essential to the Formation of Unreduced Embryo Sacs in .丝裂原活化蛋白激酶激酶激酶编码()基因对[物种名称]中未减数胚囊的形成至关重要。
Front Plant Sci. 2018 Oct 24;9:1547. doi: 10.3389/fpls.2018.01547. eCollection 2018.
10
Characterization of a strong and constitutive promoter from the Arabidopsis serine carboxypeptidase-like gene AtSCPL30 as a potential tool for crop transgenic breeding.拟南芥丝氨酸羧肽酶样基因 AtSCPL30 强启动子的特性及其在作物转基因育种中的应用。
BMC Biotechnol. 2018 Sep 21;18(1):59. doi: 10.1186/s12896-018-0470-x.

本文引用的文献

1
A polyethylene glycol-mediated protoplast transformation system for production of fertile transgenic rice plants.一种用于生产可育转基因水稻植株的聚乙二醇介导的原生质体转化系统。
Plant Physiol. 1990 Jul;93(3):857-63. doi: 10.1104/pp.93.3.857.
2
Transformation of Maize Cells and Regeneration of Fertile Transgenic Plants.玉米细胞的转化与可育转基因植株的再生
Plant Cell. 1990 Jul;2(7):603-618. doi: 10.1105/tpc.2.7.603.
3
A Drosophila RNA polymerase II transcription factor contains a promoter-region-specific DNA-binding activity.一种果蝇RNA聚合酶II转录因子含有启动子区域特异性DNA结合活性。
Cell. 1984 Feb;36(2):357-69. doi: 10.1016/0092-8674(84)90229-0.
4
Transcripts of the six Drosophila actin genes accumulate in a stage- and tissue-specific manner.六种果蝇肌动蛋白基因的转录本以阶段和组织特异性的方式积累。
Cell. 1983 May;33(1):115-23. doi: 10.1016/0092-8674(83)90340-9.
5
Two Drosophila actin genes in detail. Gene structure, protein structure and transcription during development.详细介绍两个果蝇肌动蛋白基因。基因结构、蛋白质结构及发育过程中的转录。
J Mol Biol. 1983 Feb 5;163(4):533-51. doi: 10.1016/0022-2836(83)90111-0.
6
Cytochrome oxidase subunit II gene of rice has an insertion sequence within the intron.水稻细胞色素氧化酶亚基II基因在内含子中有一个插入序列。
Nucleic Acids Res. 1984 Oct 11;12(19):7305-15. doi: 10.1093/nar/12.19.7305.
7
beta-Glucuronidase from Escherichia coli as a gene-fusion marker.来自大肠杆菌的β-葡萄糖醛酸酶作为一种基因融合标记物。
Proc Natl Acad Sci U S A. 1986 Nov;83(22):8447-51. doi: 10.1073/pnas.83.22.8447.
8
Activating elements in the promoter region of the chicken beta-actin gene.鸡β-肌动蛋白基因启动子区域中的激活元件。
Gene. 1986;48(1):1-11. doi: 10.1016/0378-1119(86)90346-x.
9
Evidence that the functional beta-actin gene is single copy in most mice and is associated with 5' sequences capable of conferring serum- and cycloheximide-dependent regulation.有证据表明,功能性β-肌动蛋白基因在大多数小鼠中是单拷贝的,并且与能够赋予血清和环己酰亚胺依赖性调控的5'序列相关。
Mol Cell Biol. 1988 Jan;8(1):480-5. doi: 10.1128/mcb.8.1.480-485.1988.
10
Development of retrovirus vectors useful for expressing genes in cultured murine embryonal cells and hematopoietic cells in vivo.用于在培养的小鼠胚胎细胞和体内造血细胞中表达基因的逆转录病毒载体的开发。
J Virol. 1988 Oct;62(10):3795-801. doi: 10.1128/JVI.62.10.3795-3801.1988.