miR156-targeted SPL10 controls Arabidopsis root meristem activity and root-derived de novo shoot regeneration via cytokinin responses

被引:77
作者
Barrera-Rojas, Carlos Hernan [1 ,2 ]
Braga Rocha, Gabriel Henrique [1 ]
Polverari, Laura [3 ]
Pinheiro Brito, Diego Armando [1 ]
Batista, Diego Silva [4 ]
Notini, Marcela M. [1 ]
Ferreira da Cruz, Ana Claudia [4 ]
Ortiz Morea, Edna Gicela [1 ,2 ]
Sabatini, Sabrina [3 ]
Otoni, Wagner Campos [4 ]
Silveira Nogueira, Fabio Tebaldi [1 ]
机构
[1] Univ Sao Paulo, Dept Biol Sci, Lab Mol Genet Plant Dev, Escola Super Agr Luiz de Queiroz, BR-13418900 Piracicaba, SP, Brazil
[2] State Univ Sao Paulo, Biosci Inst, BR-18618970 Botucatu, SP, Brazil
[3] Univ Roma La Sapienza, Lab Funct Genom & Prote Model Syst, Dipartimento Biol & Biotecnol, I-00185 Rome, Italy
[4] Univ Fed Vicosa, Dept Plant Biol, Plant Tissue Culture Lab BIOAGRO, BR-36570900 Vicosa, MG, Brazil
基金
巴西圣保罗研究基金会;
关键词
Arabidopsis thaliana; de novo shoot regeneration; meristem; microRNA156; root; SPLs; GENOME-WIDE IDENTIFICATION; CELL-DIVISION; TRANSCRIPTION FACTOR; GENE-EXPRESSION; MEDIATED TRANSFORMATION; STEM-CELLS; THALIANA; MIR156; GROWTH; DIFFERENTIATION;
D O I
10.1093/jxb/erz475
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Root growth is modulated by different factors, including phytohormones, transcription factors, and microRNAs (miRNAs). MicroRNA156 and its targets, the SQUAMOSA PROMOTER BINDING PROTEIN-LIKE (SPL) genes, define an age-dependent pathway that controls several developmental processes, including lateral root emergence. However, it remains unclear whether miR156-regulated SPLs control root meristem activity and root-derived de novo shoot regeneration. Here, we show that MIR156 and SPL genes have opposing expression patterns during the progression of primary root (PR) growth in Arabidopsis, suggesting that age cues may modulate root development. Plants with high miR156 levels display reduced meristem size, resulting in shorter primary root (PRs). Conversely, plants with reduced miR156 levels show higher meristem activity. Importantly, loss of function of SPL10 decreases meristem activity, while SPL10 de-repression increases it. Meristem activity is regulated by SPL10 probably through the reduction of cytokinin responses, via the modulation of type-B ARABIDOPSIS RESPONSE REGULATOR1(ARR1) expression. We also show that SPL10 de-repression in the PRs abolishes de novo shoot regenerative capacity by attenuating cytokinin responses. Our results reveal a cooperative regulation of root meristem activity and root-derived de novo shoot regeneration by integrating age cues with cytokinin responses via miR156-targeted SPL10.
引用
收藏
页码:934 / 950
页数:17
相关论文
共 85 条
[61]   Auxin gradients trigger de novo formation of stem cells during somatic embryogenesis [J].
Su, Ying Hua ;
Zhang, Xian Sheng .
PLANT SIGNALING & BEHAVIOR, 2009, 4 (07) :574-576
[62]   Arabidopsis Regeneration from Multiple Tissues Occurs via a Root Development Pathway [J].
Sugimoto, Kaoru ;
Jiao, Yuling ;
Meyerowitz, Elliot M. .
DEVELOPMENTAL CELL, 2010, 18 (03) :463-471
[63]   Hormonal control of cell division and elongation along differentiation trajectories in roots [J].
Takatsuka, Hirotomo ;
Umeda, Masaaki .
JOURNAL OF EXPERIMENTAL BOTANY, 2014, 65 (10) :2633-2643
[64]   Root growth in Arabidopsis requires gibberellin/DELLA signalling in the endodermis [J].
Ubeda-Tomas, Susana ;
Swarup, Ranjan ;
Coates, Juliet ;
Swarup, Kamal ;
Laplaze, Laurent ;
Beemster, Gerrit T. S. ;
Hedden, Peter ;
Bhalerao, Rishikesh ;
Bennett, Malcolm J. .
NATURE CELL BIOLOGY, 2008, 10 (05) :625-628
[65]   Aux/IAA proteins repress expression of reporter genes containing natural and highly active synthetic auxin response elements [J].
Ulmasov, T ;
Murfett, J ;
Hagen, G ;
Guilfoyle, TJ .
PLANT CELL, 1997, 9 (11) :1963-1971
[66]   The more and smaller cells mutants of Arabidopsis thaliana identify novel roles for SQUAMOSA PROMOTER BINDING PROTEIN-LIKE genes in the control of heteroblasty [J].
Usami, Takeshi ;
Horiguchi, Gorou ;
Yano, Satoshi ;
Tsukaya, Hirokazu .
DEVELOPMENT, 2009, 136 (06) :955-964
[67]   AGROBACTERIUM-TUMEFACIENS-MEDIATED TRANSFORMATION OF ARABIDOPSIS-THALIANA ROOT EXPLANTS BY USING KANAMYCIN SELECTION [J].
VALVEKENS, D ;
VANMONTAGU, M ;
VANLIJSEBETTENS, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (15) :5536-5540
[68]   Protocol: a highly sensitive RT-PCR method for detection and quantification of microRNAs [J].
Varkonyi-Gasic, Erika ;
Wu, Rongmei ;
Wood, Marion ;
Walton, Eric F. ;
Hellens, Roger P. .
PLANT METHODS, 2007, 3 (1)
[69]   Functional redundancy of PIN proteins is accompanied by auxindependent cross-regulation of PIN expression [J].
Vieten, A ;
Vanneste, S ;
Wisniewska, J ;
Benková, E ;
Benjamins, R ;
Beeckman, T ;
Luschnig, C ;
Friml, J .
DEVELOPMENT, 2005, 132 (20) :4521-4531
[70]   Dual effects of miR156-targeted SPL genes and CYP78A5/KLUH on plastochron length and organ size in Arabidopsis thaliana [J].
Wang, Jia-Wei ;
Schwab, Rebecca ;
Czech, Benjamin ;
Mica, Erica ;
Weigel, Detlef .
PLANT CELL, 2008, 20 (05) :1231-1243