Knowledge Management System of Kunming Institute of Botany,CAS
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 | |
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 |
2013-03-29 | |
发表期刊 | PLOS ONE |
ISSN | 1932-6203 |
卷号 | 8期号:3页码:e59576 |
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. |
关键词 | Protein-kinase Salt Tolerance Arabidopsis Versatile Cloning Expression System Genes Transformation Encodes |
学科领域 | Science & Technology - Other Topics |
收录类别 | SCI |
语种 | 英语 |
WOS记录号 | WOS:000317263900018 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | http://ir.kib.ac.cn/handle/151853/16513 |
专题 | 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. |
条目包含的文件 | 下载所有文件 | |||||
文件名称/大小 | 文献类型 | 版本类型 | 开放类型 | 使用许可 | ||
Wang-2013-A Series o(2267KB) | 开放获取 | -- | 浏览 下载 |
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。
修改评论