LATERAL ORGAN BOUNDARIES DOMAIN transcription factors direct callus formation in Arabidopsis regeneration

被引:297
作者
Fan, Mingzhu [1 ]
Xu, Chongyi [1 ]
Xu, Ke [1 ]
Hu, Yuxin [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Bot, Key Lab Plant Mol Physiol, Beijing 100093, Peoples R China
[2] Natl Ctr Plant Gene Res, Beijing 100101, Peoples R China
基金
中国国家自然科学基金;
关键词
LBD; callus formation; auxin; regeneration; Arabidopsis; AUXIN-RESPONSE-FACTOR; ROOT-FORMATION; SHOOT DEVELOPMENT; GENE FAMILY; MEDIATED TRANSFORMATION; CELL DEDIFFERENTIATION; TISSUE-CULTURE; IN-VITRO; THALIANA; EXPRESSION;
D O I
10.1038/cr.2012.63
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The remarkable regeneration capability of plant tissues or organs under culture conditions has underlain an extensive practice for decades. The initial step in plant in vitro regeneration often involves the induction of a pluripotent cell mass termed callus, which is driven by the phytohormone auxin and occurs via a root development pathway. However, the key molecules governing callus formation remain unknown. Here we demonstrate that Arabidopsis LATERAL ORGAN BOUNDARIES DOMAIN (LBD)/ASYMMETRIC LEAVES2-LIKE (ASL) transcription factors are involved in the control of callus formation program. The four LBD genes downstream of AUXIN RESPONSE FACTORs (ARFs), LBD16, LBD17, LBD18 and LBD29, are rapidly and dramatically induced by callus-inducing medium (CIM) in multiple organs. Ectopic expression of each of the four LBD genes in Arabidopsis is sufficient to trigger spontaneous callus formation without exogenous phytohormones, whereas suppression of LBD function inhibits the callus formation induced by CIM. Moreover, the callus triggered by LBD resembles that induced by CIM by characteristics of ectopically activated root meristem genes and efficient regeneration capacity. These findings define LBD transcription factors as key regulators in the callus induction process, thereby establishing a molecular link between auxin signaling and the plant regeneration program.
引用
收藏
页码:1169 / 1180
页数:12
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