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R K Kacker

Publications and source records attributed to R K Kacker.

4 recordsLinked to original sources

Genetic variation in Asiatic lions and Indian tigers.

Previous reports have suggested that Asiatic lions and tigers are highly inbred and exhibit very low levels of genetic variation. Our analyses on these species have shown much higher degrees of polymorphism than reported. Randomly amplified polymorphic DNA (RAPD) analysis of 38 Asiatic lions, which exist as a single population in the Gir Forest Sanctuary in India, shows an average heterozygosity of 25.82% with four primers. Sperm motility studies by our colleagues corroborate this data. In Indian tigers, microsatellite analysis of five CA repeat loci and multilocus fingerprinting using Bkm 2(8) probe on a population of 22 individuals revealed a heterozygosity of 22.65%. Microsatellite analysis of loci Fca 77 and Fca 126 revealed polymorphism amongst the Asiatic x African lion hybrids, which has enabled us to use these as markers to discriminate the pure Asiatic lions from the hybrids. A similar analysis was used to identify hybrids of Indian and Siberian tigers through polymerase chain reaction (PCR) amplification of hair samples. To ascertain the variation which existed before the population bottleneck at the turn of the present century, microsatellite analysis was performed on 50- to 125-year-old skin samples from museum specimens. Our results show similar levels of genetic variability as in the present population (21.01%). This suggests that low genetic variability may be the characteristic feature of these species and not the result of intensive inbreeding. DNA fingerprinting studies of Asiatic lions and tigers have helped in identifying individuals with high genetic variability which can be used for conservation breeding programs.

Animals↗

Consistent karyotypic abnormalities in human malignant melanomas.

Cytogenetic analysis performed on 11 human malignant melanoma cell lines that were passaged through nude mice revealed both numerical and structural types of chromosomal defects. Banding analysis showed structural anomalies in chromosomes 1, 3, 5, 6, 7, 9, 10, 11, 14 and 15. Of these, the most frequently involved chromosomes were 6, 7, and 9. Chromosomes 3 and 11 were next with chromosomes 5 and 10, the least involved. Our results were very similar to results published in the literature on melanoma cytogenetics except that we found additional chromosomal alterations. Most frequently involved structural anomalies of the short arm of chromosome 9 and the long arm of chromosome 6 have been interpreted as primary and secondary defects, respectively, in melanocyte oncogenesis.

Adult↗