4.5 Article

Flow cytometry and start codon targeted (SCoT) genetic fidelity assessment of regenerated plantlets in Tylophora indica (Burm.f.) Merrill

Journal

PLANT CELL TISSUE AND ORGAN CULTURE
Volume 150, Issue 1, Pages 129-140

Publisher

SPRINGER
DOI: 10.1007/s11240-022-02254-z

Keywords

2C DNA; In vitro proliferation; Somatic embryogenesis; Organogenesis; Micropropagation; Histology; SEM

Funding

  1. Hamdard National Foundation

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An efficient regeneration method has been developed in Tylophora indica, with histology and molecular markers indicating genetic homogeneity of the regenerated population. This study is important for addressing the challenges of large scale propagation of the plant in the wild.
Key message An efficient regeneration method has been developed in T. indica. Histology and SEM indicated somatic embryogenesis based morphogenesis. 2C genome size and SCoT marker revealed genetic homogeneity of the regenerated population. Tylophora indica (Burm.f.) Merrill. is a pharmacologically important plant, popular for alkaloidal and non-alkaloidal richness. Large scale propagation of T. indica is difficult in the wild as the seeds are small and the frequency of germination is very poor. In the present study, the genome size estimation of in vitro regenerated (indirect, direct and somatic embryo mediated) T. indica was made by flow cytometric method. Clonal fidelity of the regenerants was assessed using a start codon targeted (SCoT) molecular marker. Initially, the explants were inoculated on Murashige and Skoog basal medium supplemented with various concentrations of plant growth regulators like 2,4-dichlorophenoxy acetic acid (2,4-D), Kinetin, 6-benzyl amino purine (BAP) and 1-naphthalene acetic acid either singly or in combinations. The highest callus induction frequency (87.75%) was obtained in 6.7 mu M 2,4-D added MS medium which metamorphosed into progressive stages (globular, heart, torpedo, and cotyledonary) of embryos. Mature and healthy somatic embryos efficiently germinated into plantlets on 8.8 mu M BAP + 1.4 mu M GA(3) enriched MS medium. Histological and scanning electron microscopic study confirmed the above developing stages. The regenerated shoots were rooted best in 2.45 mu M Indole-3-butyric acid supplemented solid MS medium. The plants were hardened and acclimatized with 90% survivability. The flow cytometric 2C DNA content of indirect, direct and somatic embryo derived plants was 1.896 pg, 1.940 pg and 1.926 pg respectively, very similar to the mother plant (1.928 pg). SCoT marker generated a high percentage of monomorphic bands (94%) revealing similarity with the mother plant, thus ensuring genetic fidelity. To the best of our knowledge, this is perhaps the first ever report of 2C DNA content estimation and SCoT marker based genetic homogeneity study in T. indica.

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