No abstract

The mechanism and inheritance of intraflower self‐pollination in self‐pollinating variant strains of periwinkle was studied using three self‐pollinating and two non‐self‐pollinating but fully self‐fertile strains. Intraflower self‐pollination in self‐pollinating strains occurred due to the continued growth of the gynoecium beyond the base of the anthers, even after anthesis, resulting in intraflower self‐pollination. In non‐self‐pollinating strains, the stigma remained below the base of the anthers and did not come into contact with the pollen up to flower drop. Intraflower self‐pollination was found to be governed by duplicate recessive genes. The utility of the intraflower self‐pollination trait in the breeding of periwinkle cultivars is discussed.

The commonly found flower colors in periwinkle (Catharanthus roseus)--pink, white, red-eyed, and pale pink center--are reported to be governed by the epistatic interaction between four genes--A, R, W, and I. The mode of inheritance of an uncommon flower color, orange-red corolla and white eye, was studied by crossing an accession possessing this corolla color with a white flowered variety (Nirmal). The phenotype of the F(1) plants and segregation data of F(2) and backcross generations suggested the involvement of two more interacting and independently inherited genes, one (proposed symbol E) determining the presence or absence of red eye and another (proposed symbol O) determining orange-red corolla.

Periwinkle [Catharanthus roseus (L.) G. Don], an ornamental and medicinal plant, is a self-compatible, insect-pollinated plant species in which intraflower self-pollination does not occur because of spatial separation of the stigma and anthers. Recently three self-pollinating strains-MJ, VI, and OR-were identified. Self-pollination in these strains was found to be brought about by continuous increase in gynoecium length from anthesis to self-pollination, in contrast to non-self-pollinating strains, in which the stigma remained below the base of the anthers from anthesis to flower drop. Self-pollination in these strains was found to be controlled by duplicate, recessive genes. Self-pollination in strains MJ and VI was brought about by an increase in gynoecium length resulting from an increase in the length of the ovary, while in the strain OR, the increase in gynoecium length was because of an increase in the length of the style from anthesis to self-pollination. The three strains were intercrossed to determine the relationship between genes governing self-pollination in these strains. The F(1) plants and all plants of the F(2) generation of the cross MJ x VI exhibited self-pollination that was brought about by an increase in the length of the ovary, indicating that the same genes were involved in these two strains. The F(1) plants of crosses OR x MJ and OR x VI, exhibited self-pollination that was brought about by an increase in the length of the ovary, indicating that self-pollination brought about by an increase in the length of the ovary was dominant over self-pollination brought about by an increase in the length of the style. In the F(2) and backcross [(OR x MJ) x OR and (OR x VI) x OR] generations, both self-pollinating and non-self-pollinating plants were observed. The ratio of plants with self-pollination brought about by an increase in the length of the ovary, non-self-pollinating plants, and plants with self-pollination brought about by an increase in the length of the style in the F(2) and backcross generations fit 9:6:1 and 1:2:1 ratios, respectively. All plants of the backcrosses [(OR x MJ) x MJ and (OR x VI) x VI] exhibited self-pollination brought about by an increase in the length of the ovary. The results thus supported the earlier finding that self-pollination in the studied strains was controlled by duplicate, recessive genes and suggested that three alleles at two loci determine the occurrence or nonoccurrence of intraflower self-pollination in periwinkle.

Inheritance of a novel corolla colour in periwinkle [Catharanthus roseus (L) G. Don], viz. magenta, was studied by crossing an accession MJ, possessing this corolla colour, with cultivar Nirmal, possessing white corolla. The accession MJ was also crossed with another accession OR, possessing another novel corolla colour, viz. orange-red, to determine the relationship between genes governing magenta corolla and orange-red corolla. The F 1 plants of the cross MJ× Nirmal had pink corolla and red eye. In the F 2 generation, five kinds of corolla colours were observed: (i) pink corolla and red eye, (ii) rose corolla and red eye, (iii) magenta corolla and red eye, (iv) white corolla and red eye and (v) white corolla. The observed frequencies of the five kinds of plants fitted a ratio of 144:27:9:12:64. The progeny of the backcross, F 1 × MJ, segregated into three kinds of plants, (i) pink corolla and red eye, (ii) rose corolla and red eye and (iii) magenta corolla and red eye, in the ratio of 2:1:1, while the backcross, F 1 × Nirmal, segregated into two kinds of plants, (i) pink corolla and red eye and (ii) white corolla, in the ratio of 1:1. Two new genes (proposed symbols O m and J) appeared to be involved in the determination of magenta and rose corolla colours. Interaction between four independent genes R, W, O m and J, appeared to explain the observed segregation in the cross MJ × Nirmal. The F 1 plants of the cross MJ × OR had scarlet-red corolla and red eye. The segregation data of F 2 and backcross generations suggested that genes governing orange-red corolla and magenta corolla were allelic to each other. Two new and non-parental corolla colours viz., rose corolla and scarlet-red corolla, were observed in the progeny of the crosses of the present study.