Szilák L, Venetianer P, Kiss A
Institute of Biochemistry, Biological Research Center, Hungarian Academy of Sciences, Szeged.
Nucleic Acids Res. 1990 Aug 25;18(16):4659-64. doi: 10.1093/nar/18.16.4659.
The genes coding for the GGNCC specific Sau96I restriction and modification enzymes were cloned and expressed in E. coli. The DNA sequence predicts a 430 amino acid protein (Mr: 49,252) for the methyltransferase and a 261 amino acid protein (Mr: 30,486) for the endonuclease. No protein sequence similarity was detected between the Sau96I methyltransferase and endonuclease. The methyltransferase contains the sequence elements characteristic for m5C-methyltransferases. In addition to this, M.Sau96I shows similarity, also in the variable region, with one m5C-methyltransferase (M.SinI) which has closely related recognition specificity (GGA/TCC). M.Sau96I methylates the internal cytosine within the GGNCC recognition sequence. The Sau96I endonuclease appears to act as a monomer.
编码GGNCC特异性Sau96I限制酶和修饰酶的基因被克隆并在大肠杆菌中表达。DNA序列预测甲基转移酶为一种430个氨基酸的蛋白质(分子量:49,252),内切核酸酶为一种261个氨基酸的蛋白质(分子量:30,486)。未检测到Sau96I甲基转移酶和内切核酸酶之间的蛋白质序列相似性。甲基转移酶含有m5C - 甲基转移酶特有的序列元件。除此之外,M.Sau96I在可变区也与一种具有密切相关识别特异性(GGA/TCC)的m5C - 甲基转移酶(M.SinI)相似。M.Sau96I使GGNCC识别序列内的内部胞嘧啶甲基化。Sau96I内切核酸酶似乎以单体形式起作用。