Characterization of a species-specific repetitive DNA from a highly endangered wild animal, Rhinoceros unicornis, and assessment of genetic polymorphism by microsatellite associated sequence amplification (MASA)

• Published in: Gene 1999-03, Vol.228 (1), p.33-42
• Main Authors: Ali, Sher, Azfer, Md.Asim, Bashamboo, Anu, Mathur, Pradeep Kumar, Malik, Pradeep Kumar, Mathur, Vinod Behari, Raha, Atanu Kumar, Ansari, Shehnaz
• Format: Article
• Language: English
• Subjects: Animals; Blotting, Southern; Buffaloes; Camelus; Catfishes; Cattle; Columbidae; DNA - chemistry; DNA - genetics; DNA Probes; Endangered species; Female; Genome analysis; Goats; Gryllidae; Humans; Male; Mice; Microsatellite Repeats - genetics; Molecular Sequence Data; Oligonucleotide Probes - chemical synthesis; Oligonucleotides; One-horned rhino genome; Open Reading Frames; Perissodactyla - genetics; Phylogeny; Polymerase Chain Reaction; Polymorphism, Genetic; Polymorphism, Restriction Fragment Length; Rabbits; Rats; Repetitive Sequences, Nucleic Acid - genetics; Rhinoceros unicornis; Sequence Analysis, DNA; Species Specificity; Species-specific probe; Statistics as Topic; Swine
• ISSN: 0378-1119; 1879-0038
• DOI: 10.1016/S0378-1119(99)00015-3

We have cloned and sequenced a 906 bp EcoRI repeat DNA fraction from Rhinoceros unicornis genome. The contig pSS(R)2 is AT rich with 340 A (37.53%), 187 C (20.64%), 173 G (19.09%) and 206 T (22.74%). The sequence contains MALT box, NF–E1, Poly-A signal, lariat consensus sequences, TATA box, translational initiation sequences and several stop codons. Translation of the contig showed seven different types of protein motifs, among which, EGF-like domain cysteine pattern signatures and Bowman–Birk serine protease inhibitor family signatures were prominent. The presence of eukaryotic transcriptional elements, protein signatures and analysis of subset sequences in the 5′ region from 1 to 165 nt indicating coding potential (test code value=0.97) suggest possible regulatory and/or functional role(s) of these sequences in the rhino genome. Translation of the complementary strand from 906 to 706 nt and 190 to 2 nt showed proteins of more than 7 kDa rich in non-polar residues. This suggests that pSS(R)2 is either a part of, or adjacent to, a functional gene. The contig contains mostly non-consecutive simple repeat units from 2 to 17 nt with varying frequencies, of which four base motifs were found to be predominant. Zoo-blot hybridization revealed that pSS(R)2 sequences are unique to R. unicornis genome because they do not cross-hybridize, even with the genomic DNA of South African black rhino Diceros bicornis. Southern blot analysis of R. unicornis genomic DNA with pSS(R)2 and other synthetic oligo probes revealed a high level of genetic homogeneity, which was also substantiated by microsatellite associated sequence amplification (MASA). Owing to its uniqueness, the pSS(R)2 probe has a potential application in the area of conservation biology for unequivocal identification of horn or other body tissues of R. unicornis. The evolutionary aspect of this repeat fraction in the context of comparative genome analysis is discussed.