Fukuoka H, Kawata M, Takaiwa F
National Institute of Agrobiological Resources, Ibaraki, Japan.
Plant Mol Biol. 1994 Nov;26(3):899-907. doi: 10.1007/BF00028857.
Callus-specific rearranged DNA in rice (Oryza sativa L.) was isolated by in-gel reassociation procedure. Southern hybridization experiments revealed that some clones were amplified significantly in primary callus induced from scutellum tissue. Rapid amplification of these clones was observed within 2 days after plating seeds onto callus-induction medium containing 2,4-D. NAA gave no significant effect on DNA amplification event. Colony formation process from isolated protoplasts and plant regeneration process from callus showed clone-specific and process-specific fluctuation patterns of copy number. Sequence analysis of the clones suggested that most of the clones were originated from organelle DNA. Comparison of copy number fluctuation pattern of organelle functional genes with that of the clones suggested multiformity and/or construction-specific amplification of organelle DNA.
通过凝胶内重缔合程序分离出水稻(Oryza sativa L.)愈伤组织特异性重排DNA。Southern杂交实验表明,一些克隆在盾片组织诱导的初代愈伤组织中显著扩增。将种子接种到含有2,4-D的愈伤组织诱导培养基上后2天内观察到这些克隆的快速扩增。NAA对DNA扩增事件没有显著影响。分离原生质体的菌落形成过程和愈伤组织的植株再生过程显示出克隆特异性和过程特异性的拷贝数波动模式。对这些克隆的序列分析表明,大多数克隆起源于细胞器DNA。细胞器功能基因与这些克隆的拷贝数波动模式比较表明细胞器DNA具有多样性和/或结构特异性扩增。