Karyotype Stasis and Genetic Diversity in Amomum spp. from Tripura, North-East India

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Research Article | Published:

Print ISSN : 0970-4078.
Online ISSN : 2229-4473.
Website:www.vegetosindia.org
Pub Email: contact@vegetosindia.org
Doi: 10.5958/2229-4473.2018.00093.9
First Page: 52
Last Page: 58
Views: 1606


Keywords: Amomum; Karyotype; Simple Sequence Repeat (SSR); Genetic diversity; Unweighted Pair Group Method with Arithmetic Mean (UPGMA); Tripura


Abstract

The genus Amomum of Zingiberaceae comprising a large number of aromatic plants, with its main centre of distribution in North Eastern India, is facing the threat of extinction due to anthropogenic disturbances. In this study, the somatic chromosome number of two wild populations with each of three species of Amomum viz. A. maximum, A. corynostachyum and A. aromaticum from the state of Tripura was determined by modifying aceto-orcein staining technique. Additionally, genetic diversity was assessed using Simple Sequence Repeat (SSR) molecular markers. The somatic chromosome count was 2n=48 with one pair of nearly metacentric chromosomes bearing secondary constriction noted in all the species even at the population level. A considerable homogeneity in their karyotype was observed both at interspecific and intraspecific level suggesting a karyotype stasis. In contrast, SSR analyses indicated a high degree of genetic polymorphism (75.00-100.00%). UPGMA dendrogram revealed two different clusters with inherent variability between the populations. Our findings suggest that the morphological distinction among the species, which could not be resolved at cytological level probably due to intrinsic characteristic of the karyotype itself, can be assessed through SSR fingerprinting.

Amomum; Karyotype; Simple Sequence Repeat (SSR); Genetic diversity; Unweighted Pair Group Method with Arithmetic Mean (UPGMA); Tripura


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Acknowledgements

This work was supported by a BSR doctoral Fellowship from the U.G.C., New Delhi, India. KS is grateful to Dr. A. K. Banerjee, PMB Lab., IISER, Pune for providing laboratory facilities. The contribution of Dr. B. Dholakia, NCL, Pune in preparing the manuscript is thankfully acknowledged.


Author Information

Kishan Saha
Cytogenetics and Plant Biotechnology Laboratory, Department of Botany, Tripura University, Suryamaninagar-799022, Tripura, India,
saha.kshn@gmail.com
Rabindra Kumar Sinha



Sangram Sinha