Sved J A
Genetics. 1987 Jan;115(1):121-7. doi: 10.1093/genetics/115.1.121.
A two-generation crossing program was used to replace the entire chromosome complement of P strains by M strain chromosomes, the maternal contribution being from the P strain. The cytotype of chromosomally substituted females was indistinguishable from M strain cytotype, judged by the sterility of offspring from the cross of such females to P strain males. In addition, following replacement of the chromosomes, the level of DNA homologous to the P factor was sufficiently low to be explicable by low levels of P factor transposition. These results are consistent with immediate chromosomal control for the switching from P to M cytotype. However, the reverse chromosome substitution, replacing all chromosomes of an M strain with P chromosomes, did not usually lead to immediate change of cytotype properties, showing that there is a true maternal effect in the M to P direction. The absence of true maternal inheritance for P cytotype argues against models of P factor repression which depend on autonomous replication of a nonchromosomal element. The repression could still be explained by nonchromosomal copies of the P factor, provided that these are replenished from chromosomal P factors. A model is put forward in which P cytotype is due to the presence of circular P factors carrying a P factor target sequence, leading to preferential transposition of chromosomal P factors to nonchromosomal target sites.
采用两代杂交程序,用M品系的染色体替换P品系的整个染色体组,母本贡献来自P品系。通过将这种雌性与P品系雄性杂交后代的不育性判断,染色体替代雌性的细胞型与M品系细胞型无法区分。此外,在染色体替换后,与P因子同源的DNA水平足够低,可通过低水平的P因子转座来解释。这些结果与从P细胞型向M细胞型转换的即时染色体控制一致。然而,反向染色体替代,即用P染色体替换M品系的所有染色体,通常不会导致细胞型特性的即时改变,这表明在从M到P的方向上存在真正的母体效应。P细胞型不存在真正的母体遗传,这与依赖非染色体元件自主复制的P因子抑制模型相悖。如果P因子的非染色体拷贝由染色体P因子补充,那么抑制作用仍可由其解释。提出了一个模型,其中P细胞型是由于携带P因子靶序列的环状P因子的存在,导致染色体P因子优先转座到非染色体靶位点。