期刊论文

中文

华北农学报

1000-7091

2008

23

5

73-75

国家“863”项目（2006AA10A108）

本校为其他机构

运用农杆菌介导法将肌动蛋白RNAi表达载体PBI121-GhACT1转化棉花,经胚胎发生获得再生植株。非转化组培再生苗作为对照。以NPTII制备探针,Southern杂交结果表明,获得8个独立遗传转化系,其中3个系有2个拷贝插入;其余6个系为多拷贝。显微镜下观察开花后第5天的幼胚珠孔端,对照纤维长度约是RNAi载体转基因的3-5倍。成熟后绒长F测验结果表明,RNAi载体转化株与对照差异显著,RNAi转基因植株的绒长显著短于对照。说明GhACT1基因对纤维有延缓和抑制作用,并且主要作用于纤维发育早期。

Introduced the actin RNAi（interference） plasmid PBI121-GhACT1 into Coker 312 by Agrobacterium mediate method, and abtained the regenerants through somatic embryogenesis. NPTII as probes to hybridize, Southern result showed that there were two copies inserted into A5, A6 and A14 transgenic lines, the other six lines had multiple copies insertion. That declared these lines were transgenic positive lines. Observed under microscope, the young fiber on RNAi transgenic seeds was 3 - 5 fold shorter than that on tissue culture immature seeds. Analysi...