CLE3 and its homologs share overlapping functions in the modulation of lateral root formation through CLV1 and BAM1 in Arabidopsis thaliana

侧根 生物 分生组织 突变体 原基 拟南芥 拟南芥 细胞生物学 遗传学 基因
作者
Satoru Nakagami,Tsuyoshi Aoyama,Yoshikatsu Sato,Taiki Kajiwara,Takashi Ishida,Shinichiro Sawa
出处
期刊:Plant Journal [Wiley]
卷期号:113 (6): 1176-1191 被引量:1
标识
DOI:10.1111/tpj.16103
摘要

Lateral roots are important for a wide range of processes, including uptake of water and nutrients. The CLAVATA3 (CLV3)/EMBRYO SURROUNDING REGION-RELATED (CLE) 1 ~ 7 peptide family and their cognate receptor CLV1 have been shown to negatively regulate lateral root formation under low-nitrate conditions. However, little is known about how CLE signaling regulates lateral root formation. A persistent obstacle in CLE peptide research is their functional redundancies, which makes functional analyses difficult. To address this problem, we generate the cle1 ~ 7 septuple mutant (cle1 ~ 7-cr1, cr stands for mutant allele generated with CRISPR/Cas9). cle1 ~ 7-cr1 exhibits longer lateral roots under normal conditions. Specifically, in cle1 ~ 7-cr1, the lateral root density is increased, and lateral root primordia initiation is found to be accelerated. Further analysis shows that cle3 single mutant exhibits slightly longer lateral roots. On the other hand, plants that overexpress CLE2 and CLE3 exhibit decreased lateral root lengths. To explore cognate receptor(s) of CLE2 and CLE3, we analyze lateral root lengths in clv1 barely any meristem 1(bam1) double mutant. Mutating both the CLV1 and BAM1 causes longer lateral roots, but not in each single mutant. In addition, genetic analysis reveals that CLV1 and BAM1 are epistatic to CLE2 and CLE3. Furthermore, gene expression analysis shows that the LATERAL ORGAN BOUNDARIES DOMAIN/ASYMMETRIC LEAVES2-LIKE (LBD/ASL) genes, which promote lateral root formation, are upregulated in cle1 ~ 7-cr1 and clv1 bam1. We therefore propose that CLE2 and CLE3 peptides are perceived by CLV1 and BAM1 to mediate lateral root formation through LBDs regulation.
最长约 10秒,即可获得该文献文件

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
1秒前
汉堡包应助一只盒子采纳,获得10
3秒前
冷静的棒棒糖完成签到,获得积分10
3秒前
sparks发布了新的文献求助10
4秒前
lyyyy完成签到,获得积分10
4秒前
5秒前
寒冷的机器猫完成签到,获得积分10
6秒前
领导范儿应助aann采纳,获得10
6秒前
XHX完成签到,获得积分10
7秒前
哇卡哇卡完成签到,获得积分10
7秒前
NexusExplorer应助冯小Q采纳,获得10
7秒前
echo完成签到 ,获得积分10
8秒前
现代书雪发布了新的文献求助10
9秒前
15秒前
CipherSage应助liuyulu615采纳,获得10
17秒前
17秒前
一只盒子发布了新的文献求助10
20秒前
冯小Q发布了新的文献求助10
21秒前
瘦瘦谷槐完成签到,获得积分10
28秒前
科研小民工应助Tayzon采纳,获得50
29秒前
雨木目完成签到,获得积分10
32秒前
大个应助橘猫采纳,获得10
36秒前
烂漫剑发布了新的文献求助10
37秒前
李爱国应助caihong1采纳,获得10
44秒前
46秒前
xxvvxx发布了新的文献求助20
47秒前
快乐慕灵完成签到,获得积分10
49秒前
斯文的傲珊完成签到,获得积分10
49秒前
52秒前
欣喜豁发布了新的文献求助10
52秒前
无情鼠标完成签到,获得积分10
53秒前
caihong1发布了新的文献求助10
56秒前
yanjiuhuzu完成签到,获得积分10
1分钟前
楼祥完成签到 ,获得积分20
1分钟前
Jason完成签到,获得积分10
1分钟前
1分钟前
靓丽珩发布了新的文献求助10
1分钟前
害怕的听筠完成签到,获得积分10
1分钟前
高高的坤完成签到 ,获得积分10
1分钟前
酥瓜完成签到 ,获得积分10
1分钟前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024) 3000
Continuum Thermodynamics and Material Modelling 2000
Encyclopedia of Geology (2nd Edition) 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
Maneuvering of a Damaged Navy Combatant 650
China—Art—Modernity: A Critical Introduction to Chinese Visual Expression from the Beginning of the Twentieth Century to the Present Day 360
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3776915
求助须知:如何正确求助?哪些是违规求助? 3322325
关于积分的说明 10209854
捐赠科研通 3037674
什么是DOI,文献DOI怎么找? 1666792
邀请新用户注册赠送积分活动 797658
科研通“疑难数据库(出版商)”最低求助积分说明 757998