CONTENTS
Contents of 41(2) 2013 - acharya ng ranga agricultural university
Contents of 41(2) 2013 - acharya ng ranga agricultural university
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J.Res. ANGRAU 41(2) 26-32, 2013<br />
ASSESSMENT OF GENETIC DIVERSITY IN Capsicum spp. BY USING<br />
MORPHOLOGICAL AND MOLECULAR TOOLS<br />
S. JOSHI, C. SARMA, C. JANGID AND H.V. VIJAYAKUMARSWAMY<br />
Department of Plant Biotechnology, University of Agricultural Sciences, Bengaluru - 560065<br />
Date of Receipt : 22.12.2013 Date of Acceptance : 16.03.2013<br />
ABSTRACT<br />
Chilli belongs to the genus Capsicum which possess enormous wealth of genetic diversity. Extent of<br />
genetic diversity determines the success level of crop improvement programme. In the present study, genotypes<br />
were taken from different eco-geographical regions to assess genetic diversity and variability at both morphological<br />
and molecular level. For morphological characterization different yield attributing characters were studied. For<br />
estimation of D2 values GENRES software was used and it was found that all the exotic genotypes and genotypes<br />
from northern part of India clustered together while, two genotypes of southern part of India fell into separate cluster.<br />
Genetic diversity was also estimated at molecular level with the help of capsicum specific SSR markers, Genotype<br />
EC 362980 which belongs to Capsicum chinese and EC 121489 which belongs to Capsicum baccatum were far<br />
apart in dendrogram which showed they were less relative to each other during course of evolution. However, the<br />
remaining genotypes which belongs to Capsicum annum came in between those two species which showed they<br />
might have originated from Capsicum chinense and Capsicum baccatum.<br />
Capsicum is one of the most important spices<br />
cum vegetable crops grown in India. It belongs to<br />
family Solanaceae comprising twenty to thirty species<br />
of new world tropic and subtropics. Modern<br />
taxonomists recognize five major cultivated species<br />
of hot pepper and mild types as Capsicum annum,<br />
Capsicum fruitescense L., Capsicum chinense<br />
jacquin, Capsicum pendulum Wildenow and Capsicum<br />
pubescens Ruig and Pavon (Pickersgill, 1997). Chilli<br />
valued for its characteristic pungency, color and<br />
flavor, besides being rich source of vitamins viz. A,<br />
C and E. India is the largest producer of chilli in the<br />
world (Singh, 2007). An important way to increase<br />
productivity in any crop plant is to first select<br />
desirable genotypes from among the existing<br />
variations and use them in the breeding programmes.<br />
The extent of initial variability/genetic diversity<br />
determines the level of success of crop improvement<br />
programmes. Diversity based on morphological<br />
marker has limitations because of their small number,<br />
while diversity at biochemical level is stage<br />
depending. Molecular markers has an advantage over<br />
these limitations. However, the present study has<br />
been designed to use both morphological and<br />
molecular markers to study diversity among<br />
Capsicum germplasm.<br />
MATERIALS AND METHODS<br />
The experimental material consists of<br />
nineteen cultivars (Table.1) which were sown in poly<br />
bags inside greenhouse and then transplanted to the<br />
main field of Department of Plant Biotechnology, UAS-<br />
GKVK, Bangalore at 30 DAS during Kharif 2010 and<br />
molecular analysis with Capsicum specific primers<br />
were carried out further. Genotypes were evaluated<br />
for eight morphological characters i.e. plant height<br />
(cm), days to 1st flowering, days to 50% flowering,<br />
days to fruit maturity, seed weight (g), fruit length<br />
(cm), fruit weight (g) and number of seeds per plant.<br />
The layout of the experiment was Randomized Block<br />
Design (RBD) with three replications. The mean<br />
values of five randomly selected plants from each<br />
replication were used for data analysis, range, GCV,<br />
PCV, heritability and expected genetic advance as<br />
percent of mean were analyzed. Morphological<br />
diversity among the selected genotypes was<br />
assessed with the help of GENRES software.<br />
A total of twenty-five SSR markers which<br />
are distributed across the genome used for<br />
polymorphism studies (Table 2). For PCR reaction,<br />
20l reaction mixture containing template DNA 2.0l<br />
(20ng/l), 2.0l of both forward and reverse primer<br />
respectively (5 pm/l). 0.20l Taq DNA polymerase<br />
email: shourabhforbt@gmail.com<br />
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