Abstract

Random amplified polymorphic DNA (RAPD) markers were employed for characterization, assessment of genetic variation and inferring relationships among six variants of Canna indica L. A total of 198 RAPD bands ranging from 200 bp to 3 kbp were generated by all the six variants. Among them, most of the bands were found to be polymorphic, four band were unique of which two bands (OPA022000 and OPA043000) were observed in the variant 2 (small red) and the other two (OPA013000 and OPA053000) were noticed in the variant 4 (orange), and the remaining bands were found to be monomorphic. The pair-wise genetic distance was determined among the six variants that ranged from 0.1446 to 0.6554. A dendogram was constructed based on the RAPD profiling to infer the relationship among the six variants of C. indica that resulted in two major clusters: the first one contained two variants, viz. variant 1 (local red) and variant 2 (small red), while the second cluster composed of the remaining four variants. The results as revealed from the RAPD analysis were found congruent with those of morphological and anatomical investigation of the species.
 Bangladesh J. Plant Taxon. 28(1): 75-81, 2021 (June)

Highlights

  • The family Cannaceae, comprising the single genus Canna L. is widely distributed throughout the tropical regions

  • The present study aimed at assessing genetic variation and relationships among the six variants of Canna indica occurring in Bangladesh for the first time

  • Random amplified polymorphic DNA (RAPD) fingerprints: The present study revealed a total of 198 RAPD fingerprints generated by five oligonucleotide primers ranging from 200 bp to 3 kbp in six variants of Canna indica

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Summary

Introduction

The family Cannaceae, comprising the single genus Canna L. is widely distributed throughout the tropical regions. Molecular studies to assess genetic variation in Canna indica are lacking in Bangladesh. Because of universality and reproducibility the RAPD markers were employed to detect genetic diversity of Canna indica.

Results
Conclusion
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