VP16 fusion efficiently reveals the function of transcriptional repressors in Arabidopsis

抑制因子 生物 GATAD2B型 基因 抄写(语言学) 转录因子 YY1年 遗传学 融合蛋白 拟南芥 转录调控 心理压抑 激活剂(遗传学) 表型 功能(生物学) 细胞生物学 基因表达 发起人 突变体 重组DNA 语言学 哲学
作者
Sumire Fujiwara,Keiko Kigoshi,Nobutaka Mitsuda,Kaoru Suzuki,Masaru Ohme‐Takagi
出处
期刊:Plant Biotechnology [Japanese Society for Plant Biotechnology]
卷期号:31 (2): 123-132 被引量:10
标识
DOI:10.5511/plantbiotechnology.14.0121a
摘要

Proper gene expression regulated by transcription factors is essential for plants to achieve proper growth and development. However, the biological functions of many transcription factors remain largely unknown. Furthermore, although there are transcription factors which possess a plant-specific repression domain(s), their biological functions and whether such transcription factors function as transcriptional repressors are unclear. Thus, aiming for searching clues to understand their functions, we generated transgenic plants in which a putative transcriptional repressor fused with a VP16 viral trans-activation domain was expressed constitutively. Several plants with strong morphological phenotypes such as leaf and flower development defects were isolated from those lines expressing potential transcriptional repressors with unknown functions, giving the clue to reveal the yet-to-be analyzed functions of each protein. Reversal of function of the well-known transcriptional and floral repressor SHORT VEGETATIVE PHASE by VP16 fusion was observed, exemplifying successful functional reversion by this system. Plants constitutively expressing VP16 fused WUSCHEL, which is known to function both as a transcriptional activator and repressor, showed both phenotypes reported in its overexpression and loss-of-function lines. Taken together, our data provide examples showing the efficacy of VP16 fusion to provide helpful information to uncover the unknown functions of potential transcriptional repressors. This technique could also be effective to produce "super plants" which obtained strong and useful traits for application by strongly activating genes which are usually silent.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
所所的应助被科研通管家采纳,获得10
刚刚
酷波er的应助被科研通管家采纳,获得10
1秒前
李健的应助被科研通管家采纳,获得10
1秒前
1秒前
1秒前
啄米鸡完成签到,获得积分10
1秒前
1秒前
桐桐的应助被科研通管家采纳,获得10
1秒前
1秒前
酷波er的应助被科研通管家采纳,获得10
1秒前
2秒前
HIbiscusqian完成签到 ,获得积分10
2秒前
3秒前
aaaa发布了新的文献求助10
4秒前
梧桐树完成签到,获得积分20
4秒前
对手发布了新的文献求助10
5秒前
6秒前
热情的巧曼完成签到,获得积分10
6秒前
涛器发布了新的文献求助10
9秒前
栋栋完成签到 ,获得积分10
10秒前
科研通AI6.2的应助被坦率帅哥采纳,获得10
10秒前
11秒前
我不是马铃薯头完成签到,获得积分10
12秒前
RAN18发布了新的文献求助10
12秒前
大模型的应助被qqq采纳,获得10
12秒前
add完成签到,获得积分20
13秒前
科研通AI6.4的应助被坦率采纳,获得10
13秒前
15秒前
情怀的应助被aaaa采纳,获得10
16秒前
可乐冰红茶完成签到,获得积分10
16秒前
李洪卓发布了新的文献求助20
17秒前
春秋完成签到,获得积分10
17秒前
bkagyin的应助被GRY采纳,获得10
17秒前
渡人舟的应助被积极的尔岚采纳,获得10
18秒前
18秒前
19秒前
molihuakai的应助被叶武林采纳,获得10
19秒前
lixiang完成签到,获得积分10
19秒前
wpx驳回了ding的应助
19秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
自動車の空力技術 800
Essentials of Carbohydrate Chemistry and Biochemistry, 4th Edition 800
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Issues in Task-Based Language Teaching 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7784000
求助须知:如何正确求助?哪些是违规求助? 9323286
关于积分的说明 20393855
捐赠科研通 7372632
什么是DOI,文献DOI怎么找? 3320849
关于科研通互助平台的介绍 2468807
邀请新用户注册赠送积分活动 2337082