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Gonoproktopterus curmuca, a cultivable food and ornamental fish is found in the rivers originating from
the biodiversity hotspot - the Western Ghats, India. It is one of the prioritized species for the region-
specific aquaculture in India. G. curmuca has drastically declined in the rivers due to over-exploitation
and habitat alteration. Captive breeding and milt cryopreservation of the species have been developed
by the National Bureau of Fish Genetic Resources. Documentation of genetic variation at intra-specific
level through genetically controlled markers is of vital importance for evolving fisheries management
and aquaculture strategies; and in planning propagation assisted rehabilitation programmes. To explore
the genetic variation in natural populations of this species in Periyar, Chalakkudy and Chaliyar Rivers
(Kerala, India) allozymes, microsatellites and RAPD markers were employed. In allozyme analysis, 12
polymorphic enzymes yielded 29 loci with a total of 31 alleles. Only one private allele was recorded - in
Chaliyar with LDH locus. For microsatellite analysis, eight single locus primers from 6 cyprinids were
cross-primed in G. curmuca producing 8 presumptive microsatellite loci and a total of 53 alleles. All the
8 loci contained repeat regions (NCBI #s DQ780015, DQ780014, EF582608, EF582609, EF582610,
EF582611, EF582612 and EF582613) and were polymorphic (100%). Analysis of microsatellite data
using MICROCHECKER ruled out occurrence of null alleles. There were 4 private alleles in Periyar, 2 in
Chalakkudy and 3 in Chaliyar. The positive FIS and lesser observed heterozygosity values in many
allozymes and microsatellites loci indicated deficiency of heterozygotes and deviation from Hardy-
Weinberg equilibrium. The pair wise FST and RST; and AMOVA between riverine locations indicated
significant genetic heterogeneity (P<0.001) between populations. The allozyme and microsatellite loci
indicated significant genetic bottleneck in all the populations of G. curmuca under the Infinite Allele
Model and Two Phased Model respectively (Wilcoxon Test P<0.05). In RAPD analysis, 9 OPERON
oligonucleotide decamers produced 117 amplicons in three populations. Forty one RAPD fragments
were identified as stock specific markers. The coefficient of genetic differentiation (GST) (P<0.05) and
Nei’s (1978) unbiased genetic distance among populations indicated significant genetic differentiation
between populations. In conclusion, the genetic markers demonstrated striking genetic differentiation
between G. curmuca populations. Geographic isolation is likely to be the factor for the restricted gene
flow between the river systems. The inbreeding as a result of over-exploitation might be the reason for
the deficiency of heterozygosity and genetic bottleneck. For propagation assisted-rehabilitation, large
effective breeding population of the species may be developed with out mixing individuals from the
rivers.
(Abstract submitted online on 30 April 2009). (pp. 35-36 of ISGA X Book of Abstracts 270p.)
1
Ref. No. OP014
18 May 2009
Dear Dr.Gopalakrishnan A,
has been accepted for Oral Presentation at the 10th International Symposium on Genetics in Aquaculture
(ISGA2009) to be held on 22-26 June 2009, at the Bangkok Convention Centre and Sofitel Centara Grand
Hotel, Bangkok, THAILAND.
Please note that all presenters are required to submit and test their presentation file at the Conference-
Technical Room at least 3 hours before the time of presentation. Details regarding instructions for
presentation will be announced on www.isga2009.org.
Presentation 2 - Poster PP140; Lakra Wazir S & Gopalakrishnan, A. Marine Molecular Biology and
Biotechnology Research in India. (pp. 243 - 244 in the Abstract Book).
Yours sincerely,
Secretariat Office
Department of Aquaculture,
Faculty of Fisheries, Kasetsart University
Bangkok 10900, Thailand
Phone/Fax: +66-2-561-0990
Email: info@isga2009.org