Adenosine monophosphate enhances callus regeneration competence for de novo plant organogenesis
作者机构:Department of ChemistrySeoul National UniversitySeoul 08826Korea Plant Genomics and Breeding InstituteSeoul National UniversitySeoul 08826Korea Integrated Metabolomics Research GroupWestern Seoul CenterKorea Basic Science InstituteSeoul 03759Korea Biological Resource CenterKorea Research Institute of Bioscience and BiotechnologyJeongeup56212Korea Plant Systems Engineering Research CenterKorea Research Institute of Bioscience and BiotechnologyDaejeon 34141Korea College of PharmacyChung-Ang UniversitySeoul 06974Korea
出 版 物:《Molecular Plant》 (分子植物(英文版))
年 卷 期:2023年第16卷第12期
页 面:1867-1870页
核心收录:
学科分类:0710[理学-生物学] 071001[理学-植物学] 07[理学]
基 金:Basic Science Research(NRF-2022R1A2 B5B02001266 to P.J.S.) the New breeding technologies development Program(PJ01653002 to P.J.S.)provided by the Rural Development Administration This work was also supported by Korea Basic Science Institute(C370000 to G.S.H) the Korea Research Institute of Bioscience and Biotechnology(KRIBB)Research Initiative Program(KGM 5282331 to S.W.K.)
摘 要:Dear Editor,Plant tissue culture involves callus formation and de novo shoot ***,explants from differentiated tissues are used to generate a pluripotent cell mass,called callus,on auxin-rich callus-inducing medium(CIM),followed by shoot regeneration on cytokinin-rich shoot-inducing medium(SiM).Callus results from division of pericycle-like cells(Atta et al.,2009;Sugimoto et al.,2010);its cellular identity resembles that of lateral root primordia(Atta et al.,2009;Sugimoto et al.,2010).Callus acquires cellular pluripotency by forming root stem cell niches on CIM(Sugimoto et al.,2010)。