Aquat. Living Resour.
Volume 17, Number 1, January-March 2004
|Page(s)||31 - 34|
|Published online||15 January 2004|
Identification of four mud crab species (genus Scylla) using ITS-1 and 16S rDNA markers
Faculty of Science, University of the Ryukyus, Nishihara, Okinawa
2 Tungkang Marine Laboratory, Taiwan Fisheries Research Institute, Tangkang, Pingtung, Taiwan 928, Republic of China
3 Yaeyama Station, National Center for Stock Enhancement, Fisheries Research Agency (FRA) and Ishigaki Tropical Station, Seikai National Fisheries Research Institute, FRA, Ishigaki, Okinawa 907-0451, Japan
4 School of Marine Science and Technology, Tokai University, Shimizu, Shizuoka 424-8610, Japan
Corresponding author: firstname.lastname@example.org
Accepted: 16 December 2003
The first internal transcribed spacer (ITS-1) of nuclear ribosomal DNA and mitochondrial DNA 16S rRNA were amplified by Polymerase chain reaction (PCR) using genomic DNA extracted from adult tissue of four species of Scylla spp. and the first zoeal stages of S. serrata, S. paramamosain and S. olivacea as template. Using the ITS-1 region, variation in product fragment length was found to be useful for distinguishing S. serrata and S. olivacea from two other species. The other two species (S. paramamosain and S. tranquebarica) could be identified using the restriction endonuclease Hha I. Using 16S rDNA, all four species were identified using PCR-restriction fragment length polymorphism (RFLP) by double digestion with DraI and HindIII. These genetic markers can be used for hybridization breeding studies and in field studies of larval and juvenile mud crabs of the genus Scylla.
Key words: Larval stage / Species identification / PCR-RFLP / Mud crab / Scylla spp.
© EDP Sciences, IFREMER, IRD, 2004
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