Dissection of the AtNRT2.1:AtNRT2.2 Inducible High-Affinity Nitrate Transporter Gene Cluster

基因 基因簇 化学 转录因子 基因表达 细胞生物学 基因家族
作者
Wenbin Li,Ye Wang,Mamoru Okamoto,Nigel M. Crawford,M. Yaeesh Siddiqi,Anthony D. M. Glass
出处
期刊:Plant Physiology [Oxford University Press]
卷期号:143 (1): 425-433 被引量:244
标识
DOI:10.1104/pp.106.091223
摘要

Using a new Arabidopsis (Arabidopsis thaliana) mutant (Atnrt2.1-nrt2.2) we confirm that concomitant disruption of NRT2.1 and NRT2.2 reduces inducible high-affinity transport system (IHATS) by up to 80%, whereas the constitutive high-affinity transport system (CHATS) was reduced by 30%. Nitrate influx via the low-affinity transport system (LATS) was unaffected. Shoot-to-root ratios were significantly reduced compared to wild-type plants, the major effect being upon shoot growth. In another mutant uniquely disrupted in NRT2.1 (Atnrt2.1), IHATS was reduced by up to 72%, whereas neither the CHATS nor the LATS fluxes were significantly reduced. Disruption of NRT2.1 in Atnrt2.1 caused a consistent and significant reduction of shoot-to-root ratios. IHATS influx and shoot-to-root ratios were restored to wild-type values when Atnrt2.1-nrt2.2 was transformed with a NRT2.1 cDNA isolated from Arabidopsis. Disruption of NRT2.2 in Atnrt2.2 reduced IHATS by 19% and this reduction was statistically significant only at 6 h after resupply of nitrate to nitrogen-deprived plants. Atnrt2.2 showed no significant reduction of CHATS, LATS, or shoot-to-root ratios. These results define NRT2.1 as the major contributor to IHATS. Nevertheless, when maintained on agar containing 0.25 mm KNO3 as the sole nitrogen source, Atnrt2.1-nrt2.2 consistently exhibited greater stress and growth reduction than Atnrt2.1. Evidence from real-time PCR revealed that NRT2.2 transcript abundance was increased almost 3-fold in Atnrt2.1. These findings suggest that NRT2.2 normally makes only a small contribution to IHATS, but when NRT2.1 is lost, this contribution increases, resulting in a partial compensation.

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
研友_VZG7GZ应助科研通管家采纳,获得10
刚刚
1秒前
科研通AI2S应助科研通管家采纳,获得10
1秒前
852应助科研通管家采纳,获得10
1秒前
Copyright应助科研通管家采纳,获得10
1秒前
SciGPT应助科研通管家采纳,获得200
1秒前
weiwei发布了新的文献求助10
2秒前
orixero应助科研通管家采纳,获得10
2秒前
CodeCraft应助科研通管家采纳,获得10
2秒前
2秒前
寒冷的桐完成签到,获得积分10
2秒前
小二郎应助科研通管家采纳,获得100
2秒前
2秒前
JamesPei应助科研通管家采纳,获得10
3秒前
Hello应助科研通管家采纳,获得10
3秒前
小马甲应助科研通管家采纳,获得10
3秒前
张文乐完成签到,获得积分10
5秒前
英俊的铭应助yyd采纳,获得200
7秒前
weiwei完成签到,获得积分10
13秒前
小二郎应助Yjh采纳,获得10
13秒前
Kitty完成签到,获得积分10
17秒前
xzy998发布了新的文献求助30
19秒前
19秒前
Zero发布了新的文献求助10
19秒前
机灵曼荷完成签到,获得积分10
19秒前
七yy完成签到 ,获得积分10
21秒前
77完成签到,获得积分10
23秒前
Liuruijia完成签到 ,获得积分10
23秒前
易槐完成签到 ,获得积分10
24秒前
等待冰之完成签到 ,获得积分10
24秒前
能干的新筠完成签到,获得积分10
25秒前
NeoWu完成签到,获得积分10
25秒前
呵呵哒发布了新的文献求助10
26秒前
nojivv完成签到,获得积分10
27秒前
echo完成签到,获得积分10
27秒前
11完成签到,获得积分10
29秒前
阿苗完成签到 ,获得积分10
30秒前
zhh完成签到,获得积分10
30秒前
31秒前
高分求助中
液晶指向矢仿真分析数据集 8888
Invited Discussant 63O and 64O 1000
Ideology and Meaning-Making under the Putin Regime 750
Thermal effects on behaviour of clay–structure interface under partial drainage 500
Petrology and Plate Tectonics 500
Writing Systems 500
A Handbook of User Experience Research & Design in Libraries 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6895521
求助须知:如何正确求助?哪些是违规求助? 8591375
关于积分的说明 18242840
捐赠科研通 6291146
什么是DOI,文献DOI怎么找? 3060287
关于科研通互助平台的介绍 2078642
邀请新用户注册赠送积分活动 2038149