Hernould M, Glimelius K, Veuskens J, Bergman P, Mouras A
Department of Plant Breeding Research, Uppsala Genetic Center, Swedish University of Agricultural Sciences, Sweden.
Plant J. 1997 Sep;12(3):703-9. doi: 10.1046/j.1365-313x.1997.00703.x.
An alloplasmic male-sterile line of tobacco, containing the nucleus of Nicotiana tabacum and the cytoplasm of Nicotiana repanda, is restored to fertility by introgression of an alien chromosome fragment obtained from the cytoplasm donor. To isolate the restorer gene(s), the alien chromosome fragment was microdissected from metaphase plates of the restored line. The microdissected chromosomes represented only 0.1 pg of DNA, which was amplified using a degenerate oligonucleotide-primed PCR method (DOP-PCR), from which a chromosome fragment specific library was created. Compared with previous strategies used for microcloning, a modified and improved method was developed by the subsequent isolation of expressed sequences. The library was screened with cDNA probes synthesized by reverse transcription and DOP-PCR amplification (RT/DOP-PCR), of total RNAs isolated from early developing restored and male-sterile flower buds. By this strategy, transcribed DNA sequences specific for the restored line were cloned.
一种烟草异质质体雄性不育系,其细胞核来自烟草,细胞质来自黄花烟草,通过导入从细胞质供体获得的外源染色体片段恢复育性。为了分离恢复基因,从恢复系的中期板上显微切割出该外源染色体片段。显微切割的染色体仅代表0.1 pg的DNA,使用简并寡核苷酸引物PCR方法(DOP-PCR)进行扩增,据此构建了染色体片段特异性文库。与先前用于微克隆的策略相比,通过随后分离表达序列开发了一种改良和改进的方法。用从早期发育的恢复系和雄性不育花芽中分离的总RNA经逆转录和DOP-PCR扩增(RT/DOP-PCR)合成的cDNA探针筛选该文库。通过这种策略,克隆了恢复系特有的转录DNA序列。