De novo shoot organogenesis during plant regeneration

被引:62
|
作者
Shin, Jinwoo [1 ,3 ,4 ,5 ]
Bae, Soonhyung [1 ]
Seo, Pil Joon [1 ,2 ]
机构
[1] Seoul Natl Univ, Dept Chem, Seoul 08826, South Korea
[2] Seoul Natl Univ, Plant Genom & Breeding Inst, Seoul 08826, South Korea
[3] Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Ctr Computat & Integrat Biol, Boston, MA 02114 USA
[5] Harvard Med Sch, Dept Genet, Boston, MA 02114 USA
基金
新加坡国家研究基金会;
关键词
Callus; de novo shoot organogenesis; in vitro tissue culture; meristem; plant regeneration; pluripotency; CYTOKININ SIGNAL-TRANSDUCTION; B RESPONSE REGULATORS; CUP-SHAPED-COTYLEDON; CELL-CYCLE; ARABIDOPSIS-THALIANA; APICAL MERISTEM; ELECTRICAL CONTROL; HISTIDINE KINASE; GENE-EXPRESSION; IN-VIVO;
D O I
10.1093/jxb/erz395
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Plants exhibit remarkable regeneration capacity, ensuring developmental plasticity. In vitro tissue culture techniques are based on plant regeneration ability and facilitate production of new organs and even the whole plant from explants. Plant somatic cells can be reprogrammed to form a pluripotent cell mass called the callus. A portion of pluripotent callus cells gives rise to a fertile shoot via de novo shoot organogenesis (DNSO). Here, we reconstitute the shoot regeneration process with four phases, namely pluripotency acquisition, shoot promeristem formation, establishment of the confined shoot progenitor, and shoot outgrowth. Additionally, other biological processes, including cell cycle progression and reactive oxygen species metabolism, which further contribute to successful completion of DNSO, are also summarized. Overall, this study highlights recent advances in the molecular and cellular events involved in DNSO, as well as the regulatory mechanisms behind key steps of DNSO.
引用
收藏
页码:63 / 72
页数:10
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