Department of Agronomy, University of Missouri, Columbia, Mo. 65211.
Genetics. 1980 Aug;95(4):929-44. doi: 10.1093/genetics/95.4.929.
A planting of 3,919 M(1) kernels from normal ears crossed by EMS-treated pollen produced 3,461 M(1) plants and 3,172 selfed ears. These plants yielded 2,477 (72%) total heritable changes; the selfed ears yielded 2,457 (78%) recessive mutants, including 855 (27%) recessive kernel mutants and 8 (0.23%) viable dominant mutants. The ratio of recessive to dominant mutants was 201:1. The average mutation frequency for four known loci was three per 3,172 genomes analyzed. The estimated total number of loci mutated was 535 and the estimated number of kernel mutant loci mutated was 285. Among the 855 kernel mutants, 432 had a nonviable embryo, and 59 germinated but had a lethal seedling. A sample of 194 of the latter two types was tested for heritability, lethality, chromosome arm location and endosperm-embryo interaction between mutant and nonmutant tissues in special hyper-hypoploid combinations produced by manipulation of B-A translocations. The selected 194 mutants were characterized and catalogued according to endosperm phenotype and investigated to determine their effects on the morphology and development of the associated embryo. The possibility of rescuing some of the lethal mutants by covering the mutant embryo with a normal endosperm was investigated. Ninety of these 194 mutants were located on 17 of the 18 chromosome arms tested. Nineteen of the located mutants were examined to determine the effect of having a normal embryo in the same kernel with a mutant endosperm, and vice versa, as compared to the expression observed in kernels with both embryo and endosperm in a mutant condition. In the first situation, for three of the 19 mutants, the mutant endosperm was less extreme (the embryo helped); for seven cases, the mutant endosperm was more extreme (the embryo hindered); and for nine cases, there was no change. In the reverse situation, for four cases the normal endosperm helped the mutant embryo; for 14 cases there was no change and one case was inconclusive.
种植了 3919 个正常花粉授粉的 EMS 处理过的耳粒,得到 3461 株 M(1)代植株和 3172 个自交穗。这些植株共产生了 2477 个(72%)可遗传的变化;自交穗产生了 2457 个(78%)隐性突变体,包括 855 个(27%)隐性籽粒突变体和 8 个(0.23%)存活显性突变体。隐性突变体与显性突变体的比例为 201:1。四个已知基因座的平均突变频率为每 3172 个基因组三个。估计突变的基因座总数为 535 个,籽粒突变的基因座数为 285 个。在 855 个籽粒突变体中,有 432 个胚无活力,有 59 个萌发但幼苗致死。将后两种类型的 194 个样本进行了遗传力、致死性、染色体臂位置和突变体与非突变体组织之间胚乳-胚胎相互作用的测试,这些样本是通过操纵 B-A 易位产生的特殊超-亚倍体组合产生的。对选择的 194 个突变体进行了特征描述和分类,根据胚乳表型进行了研究,并对其对相关胚胎形态和发育的影响进行了调查。通过用正常胚乳覆盖突变体胚胎,研究了拯救一些致死突变体的可能性。在 194 个突变体中,有 90 个位于 17 个被测试的染色体臂中的 18 个。对其中的 19 个突变体进行了检测,以确定在同一个籽粒中具有正常胚乳和突变体胚乳的情况下,以及在具有突变体胚乳和胚乳的情况下,与观察到的表达情况相比,它们对胚胎的影响。在第一种情况下,对于 19 个突变体中的 3 个,突变体胚乳不那么极端(胚胎有帮助);对于 7 个案例,突变体胚乳更极端(胚胎有阻碍);对于 9 个案例,没有变化。在相反的情况下,对于 4 个案例,正常胚乳帮助了突变体胚胎;对于 14 个案例,没有变化,一个案例不确定。