Departments of Plant Breeding and Biometry, and of Vegetable Crops, Cornell University, Ithaca, N.Y., USA.
Theor Appl Genet. 1979 Sep;54(5):193-201. doi: 10.1007/BF00267707.
The expressed activity in pollen and stigma was determined for both S alleles of sixteen S-alíele heterozygous genotypes and for one of the two S alleles of two additional heterozygotes. Activities were measured using pollen tube penetration and seed set data from reciprocal crosses between each S-allele heterozygote and its two corresponding S-allele homozygotes.In pollen the S-allele activities ranged from zero to 100% inhibition of pollen tube penetration and seed set, and in the stigma they ranged from 8 to 100% inhibition. Of the sixty-eight S-allele activities measured, thirty-three (48%) were 90 to 100% inhibition, nine (13%) were 80 to 89% inhibition and one to five were within each ten-unit range below 80% inhibition.In an S-allele heterozygote, each subset of two S alleles had an activity for each allele in both pollen and stigma which was highly repeatable among duplicate pollinations within and among successive years. Each subset of two S alleles had a specific S-allele interaction in the pollen, and the same or another specific interaction in the stigma. In pairings with six other S alleles, allele S 2 had four calculated levels of activity in pollen that ranged from 88 to 94%, and five levels in the stigmas between 15 and 94%. When paired in a heterozygote, alleles S 3 and S 5 had activities ranging between 42 and 59%, representing mutual weakening of S-allele activity. Also, heterozygote S 15 S 3 had pollen activities, respectively, of 25 and 6%, i.e. mutual weakening in the pollen.These results indicate that in heterozygous combination with a series of other S alleles, each S-allele may have activity in pollen and also in stigma that potentially is between zero and 100% inhibition. They further indicate that the defined sexual-organ X S-allele-interaction Types I, II, III and IV are extremes; all intermediate variations including complete weakening of both alleles are possible. Recessiveness is weakening of the activity of but one of the two S alleles. The pollen tube penetrations into the style and seed set were highly correlated.
对十六个 S 等位基因杂合基因型的两个 S 等位基因和另外两个杂合基因型的一个 S 等位基因的花粉和柱头的表达活性进行了测定。活性通过每个 S 等位基因杂合体与其两个相应的 S 等位基因纯合体之间的正反交花粉管穿透和结实数据来测量。在花粉中,S 等位基因活性范围从完全抑制花粉管穿透和结实的 0%到 100%,在柱头中,活性范围从 8%到 100%。在所测量的 68 个 S 等位基因活性中,有 33 个(48%)为 90%到 100%抑制,9 个(13%)为 80%到 89%抑制,还有 1 到 5 个处于 80%抑制以下的每十个单位范围内。在 S 等位基因杂合体中,两个 S 等位基因的每个子集在花粉和柱头中对每个等位基因的活性在同一重复授粉和连续几年内都具有高度可重复性。两个 S 等位基因的每个子集在花粉中有特定的 S 等位基因相互作用,在柱头中有相同或另一个特定的相互作用。与其他六个 S 等位基因配对时,等位基因 S2 在花粉中具有四个活性水平,范围从 88%到 94%,在柱头中具有五个水平,范围从 15%到 94%。当在杂合体中配对时,等位基因 S3 和 S5 的活性范围在 42%到 59%之间,代表 S 等位基因活性的相互减弱。此外,杂合体 S15S3 的花粉活性分别为 25%和 6%,即花粉中相互减弱。这些结果表明,在与一系列其他 S 等位基因的杂合组合中,每个 S 等位基因在花粉和柱头中都可能具有潜在的 0%到 100%抑制活性。它们进一步表明,定义的性器官 X S 等位基因相互作用类型 I、II、III 和 IV 是极端情况;所有中间变化,包括两个等位基因的完全减弱都是可能的。隐性是两个 S 等位基因中只有一个的活性减弱。花粉管穿透花柱和结实高度相关。