Andersson G, McIver K, Hedén L O, Scott J R
Department of Microbiology, Lund University, Sweden.
Gene. 1996 Oct 10;175(1-2):77-81. doi: 10.1016/0378-1119(96)00124-2.
The gene (mga4) encoding the positive regulatory protein, Mga4, was cloned and sequenced from an M type 4 strain (AP4) of Streptococcus pyogenes. The deduced amino acid (aa) sequence of this "divergent Mga' shows 88% identity to the prototype Mga1 in its N-terminal half, which contains all three of the predicted helix-turn-helix domains. However, one of the predicted receiver domains of Mga1, which is at its C terminus, is not conserved in the Mga4 aa sequence. Nevertheless, a mutation in mga1 was found to be complemented for activation of the gene encoding M protein (emm) by mga4 in trans. This suggests that the aa residues of the C-terminal predicted receiver domain are not critical for activation of emm transcription.
从化脓性链球菌的M4型菌株(AP4)中克隆并测序了编码正调控蛋白Mga4的基因(mga4)。这种“不同的Mga”推导的氨基酸(aa)序列在其N端一半与原型Mga1显示出88%的同一性,其中包含所有三个预测的螺旋-转角-螺旋结构域。然而,Mga1预测的位于其C端的一个受体结构域在Mga4的aa序列中并不保守。尽管如此,发现mga1中的一个突变在反式中被mga4互补以激活编码M蛋白(emm)的基因。这表明C端预测的受体结构域的aa残基对于emm转录的激活并不关键。