Wintz H, Chen H C, Sutton C A, Conley C A, Cobb A, Ruth D, Hanson M R
Section of Genetics and Development, Cornell University, Ithaca, NY 14853, USA.
Plant Mol Biol. 1995 Apr;28(1):83-92. doi: 10.1007/BF00042040.
The expression of a 25 kDa protein, encoded by the fused mitochondrial pcf gene, is associated with cytoplasmic male sterility (CMS) in petunia. To investigate the role of the 25 kDa protein in CMS we have transformed petunia and tobacco plants with constructs expressing a portion of the urfS sequence of the pcf cDNA which encodes the 25 kDa protein. The urfS sequence was fused with two different mitochondrial targeting sequences. The chimeric gene coding region was placed under the control of the CaMV 35S promoter or a tapetum-specific promoter. Expression of the PCF protein was obtained in mitochondria of transgenic petunia and tobacco plants, yet fertility of the plants was not affected. Analysis of the location of the urfS-encoded protein revealed that it fractionates primarily into the soluble fraction in the transgenic plants whereas the genuine 25 kDa protein is found primarily in the soluble fraction but also in the membrane portion of immature buds from CMS petunia plants. Fertile transgenic plants were obtained which expressed the 25 kDa protein in the tapetal layer of post-meiotic anthers, while CMS plants express the endogenous 25 kDa protein in both the tapetal layer and sporogenous tissue of pre-meiotic anthers.
由融合的线粒体pcf基因编码的一种25 kDa蛋白的表达与矮牵牛的细胞质雄性不育(CMS)有关。为了研究这种25 kDa蛋白在CMS中的作用,我们用表达编码该25 kDa蛋白的pcf cDNA的urfS序列一部分的构建体转化了矮牵牛和烟草植株。urfS序列与两个不同的线粒体靶向序列融合。嵌合基因编码区置于CaMV 35S启动子或绒毡层特异性启动子的控制之下。在转基因矮牵牛和烟草植株的线粒体中获得了PCF蛋白的表达,但植株的育性未受影响。对urfS编码蛋白位置的分析表明,它在转基因植株中主要分馏到可溶性部分,而真正的25 kDa蛋白主要存在于可溶性部分,但也存在于CMS矮牵牛植株未成熟花蕾的膜部分。获得了在减数分裂后花药的绒毡层中表达25 kDa蛋白的可育转基因植株,而CMS植株在减数分裂前花药的绒毡层和造孢组织中均表达内源性25 kDa蛋白。