Research Article

Cloning and sequencing of the rDNA gene family of the water buffalo (Bubalus bubalis)

Published: August 29, 2012
Genet. Mol. Res. 11 (3) : 2878-2883 DOI: https://doi.org/10.4238/2012.July.10.3
Cite this Article:
C.Y. Pang, T.X. Deng, D.S. Tang, C.Y. Yang, H. Jiang, B.Z. Yang, X.W. Liang (2012). Cloning and sequencing of the rDNA gene family of the water buffalo (Bubalus bubalis). Genet. Mol. Res. 11(3): 2878-2883. https://doi.org/10.4238/2012.July.10.3
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Abstract

The rDNA genes coding for ribosomal RNA in animals are complicated repeat sequences with high GC content. We amplified water buffalo rDNA gene sequences with the long and accurate (LA) PCR method, using LA Taq DNA polymerase and GC buffer, based on bioinformatic analysis of related organisms. The rDNA genes were found to consist of 9016 nucleotides, including three rRNA genes and two internal transcribed spacers (ITS), which we named 18S rRNA, ITS1, 5.8S rRNA, ITS2 and 28S rRNA. We tested and optimized conditions for cloning these complicated rDNA sequences, including specific rules of primer design, improvements in the reaction system, and selection of the DNA polymerase.

The rDNA genes coding for ribosomal RNA in animals are complicated repeat sequences with high GC content. We amplified water buffalo rDNA gene sequences with the long and accurate (LA) PCR method, using LA Taq DNA polymerase and GC buffer, based on bioinformatic analysis of related organisms. The rDNA genes were found to consist of 9016 nucleotides, including three rRNA genes and two internal transcribed spacers (ITS), which we named 18S rRNA, ITS1, 5.8S rRNA, ITS2 and 28S rRNA. We tested and optimized conditions for cloning these complicated rDNA sequences, including specific rules of primer design, improvements in the reaction system, and selection of the DNA polymerase.