Plant Biotechnology Laboratory, Life Science Institute, Mitsui Toatsu Chemicals Inc., Togo 1144, 297, Mobara, Japan.
Theor Appl Genet. 1995 Jun;90(7-8):948-51. doi: 10.1007/BF00222907.
Twelve Japanese rice cultivars were converted to CMS by asymmetric protoplast fusion with MTC-5A, the cytoplasm of which was derived from an indica rice, Chinsurah Boro II. With the exception of the cybrids that had a nucleus from Hoshiyutaka, most of these cybrid plants were sterile. The unique sequence downstream from the mitochondrial atp6 of MTC-5A was specifically amplified in the sterile cybrid plants by PCR. All progenies of the cybrid plants carrying this unique sequence were sterile. On the other hand, in some of the sterile cybrid plants in which the unique sequence was not amplified by PCR, fertility was recovered in their progenies. Somaclonal mutation may have caused sterility in these cybrids. Only the cybrid plants that had the unique sequence detected by PCR were CMS. Thus, the CMS plants can be selected rapidly and easily by PCR, at an early stage of plant regeneration. Soon after transplanting the regenerated plants to a green house, fertile cybrids and sterile cybrids produced by somaclonal mutation can be removed. These findings also show that the unique region downstream from atp6 is tightly linked with the CMS phenotype.
十二种日本水稻品种通过与 MTC-5A(其细胞质来自籼稻 Chinsurah Boro II)的不对称原生质体融合转化为 CMS。除了细胞核来自 Hoshiyutaka 的杂种外,这些杂种植物大多不育。通过 PCR 特异性扩增了来自 MTC-5A 的线粒体 atp6 下游的独特序列。携带此独特序列的杂种植物的所有后代均不育。另一方面,在一些未通过 PCR 扩增该独特序列的不育杂种植物中,其后代的育性得到了恢复。体细胞突变可能导致这些杂种植物不育。只有通过 PCR 检测到独特序列的杂种植物才是 CMS。因此,可以在植物再生的早期阶段通过 PCR 快速、轻松地选择 CMS 植物。在将再生植物移植到温室后不久,就可以去除由体细胞突变产生的可育和不育杂种。这些发现还表明,atp6 下游的独特区域与 CMS 表型紧密相关。