“…Genomic DNA (500 ng) was digested and ligation was performed in 4 h at 37°C using EcoRl (or Pstl) and Msel enzymes (5 U each), 1 U of T4 ligase, 50 pmol of Mseladaptor, 5 pmol of £coRI-adaptor (or Pstl) in 1 x RL buffer (20 mM Tris-acetate, 20 mM magnesium acetate, 100 mM potassium acetate, 5 mM DTT, 2.5 mg BSA) added with ATP to a final concentration of 10 mM [36]. Then, 5 ul of seven-fold diluted digested and ligated DNA was preamplified in 20 ul reaction mixture containing 75 ng of EcoRl + N (or Pstl + N) and Msel + N primers, lx PCR buffer (50 mM MgCl, 1.5 mM MgCl 2 , 10 mM Tris-HCl), 10 mM dNTPs and 1 U of Taq DNA polymerase [39]. The Eco, Pst and Mse primers were called in tables and figures as E, P and M, respectively.…”