A Series of TA-Based and Zero-Background Vectors for Plant Functional Genomics
Wang, Chuntao1,2; Yin, Xianlun1,2; Kong, Xiangxiang1,3; Li, Wansha1,2; Ma, Lan1,3; Sun, Xudong1,2; Guan, Yanlong1,3; Todd, Christopher D.4; Yang, Yongping1,2; Hu, Xiangyang1,2
刊名PLOS ONE
2013-03-29
卷号8期号:3页码:e59576
关键词PROTEIN-KINASE SALT TOLERANCE ARABIDOPSIS VERSATILE CLONING EXPRESSION SYSTEM GENES TRANSFORMATION ENCODES
ISSN号1932-6203
通讯作者Hu, XY (reprint author), Chinese Acad Sci, Kunming Inst Bot, Key Lab Biodivers & Biogeog, Kunming, Yunna, Peoples R China. ; huxiangyang@mail.kib.ac.cn
英文摘要With the sequencing of genomes from many organisms now complete and the development of high-throughput sequencing, life science research has entered the functional post-genome era. Therefore, deciphering the function of genes and how they interact is in greater demand. To study an unknown gene, the basic methods are either overexpression or gene knockout by creating transgenic plants, and gene construction is usually the first step. Although traditional cloning techniques using restriction enzymes or a site-specific recombination system (Gateway or Clontech cloning technology) are highly useful for efficiently transferring DNA fragments into destination plasmids, the process is time consuming and expensive. To facilitate the procedure of gene construction, we designed a TA-based cloning system in which only one step was needed to subclone a DNA fragment into vectors. Such a cloning system was developed from the pGreen binary vector, which has a minimal size and facilitates construction manipulation, combined with the negative selection marker gene ccdB, which has the advantages of eliminating the self-ligation background and directly enabling high-efficiency TA cloning technology. We previously developed a set of transient and stable transformation vectors for constitutive gene expression, gene silencing, protein tagging, subcellular localization analysis and promoter activity detection. Our results show that such a system is highly efficient and serves as a high-throughput platform for transient or stable transformation in plants for functional genome research.
学科主题Science & Technology - Other Topics
WOS标题词Science & Technology
类目[WOS]Multidisciplinary Sciences
研究领域[WOS]Science & Technology - Other Topics
关键词[WOS]PROTEIN-KINASE ; SALT TOLERANCE ; ARABIDOPSIS ; VERSATILE ; CLONING ; EXPRESSION ; SYSTEM ; GENES ; TRANSFORMATION ; ENCODES
收录类别SCI
资助信息National Sciences Foundation of China [30971452, 31170256]; Major Sciences and Technology Program [110201101003-TS-03]; Young Academic and Technical Leader Raising Foundation of Yunnan Province [2012HB041]; State Education Ministry
语种英语
WOS记录号WOS:000317263900018
公开日期2013-06-08
内容类型期刊论文
源URL[http://ir.kib.ac.cn/handle/151853/16513]  
专题昆明植物研究所_中国科学院青藏高原研究所昆明部
作者单位1.Chinese Acad Sci, Kunming Inst Bot, Key Lab Biodivers & Biogeog, Kunming, Yunna, Peoples R China
2.Chinese Acad Sci, Kunming Inst Bot, Plant Germplasm & Genom Ctr, Germplasm Bank Wild Species, Kunming, Yunna, Peoples R China
3.Univ Chinese Acad Sci, Beijing, Peoples R China
4.Univ Saskatchewan, Dept Biol, Saskatoon, SK S7N 0W0, Canada
推荐引用方式
GB/T 7714
Wang, Chuntao,Yin, Xianlun,Kong, Xiangxiang,et al. A Series of TA-Based and Zero-Background Vectors for Plant Functional Genomics[J]. PLOS ONE,2013,8(3):e59576.
APA Wang, Chuntao.,Yin, Xianlun.,Kong, Xiangxiang.,Li, Wansha.,Ma, Lan.,...&Hu, Xiangyang.(2013).A Series of TA-Based and Zero-Background Vectors for Plant Functional Genomics.PLOS ONE,8(3),e59576.
MLA Wang, Chuntao,et al."A Series of TA-Based and Zero-Background Vectors for Plant Functional Genomics".PLOS ONE 8.3(2013):e59576.
个性服务
查看访问统计
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。


©版权所有 ©2017 CSpace - Powered by CSpace