Maekawa T, Ohtsubo E
Institute of Molecular and Cellular Biosciences, University of Tokyo, Japan.
Jpn J Genet. 1994 Jun;69(3):269-85. doi: 10.1266/jjg.69.269.
To analyze the region that determines the specificity of binding of the Tn3 transposase to the terminal inverted repeat sequences (IR), we first determined the nucleotide sequence of a Tn3-family transposon, gamma delta, which is supposed to encode a transposase similar to that of Tn3. gamma delta was 5981 bp in length and contained three coding frames: Two were the genes, tnpA and tnpR, encoding transposase (1002 amino acids) and resolvase/repressor (183 amino acids), respectively, and the third, named tnpX, encoding a protein (698 amino acids) of unknown function but containing two NTP-binding motifs. Utilizing the tnpA sequence, we then constructed a series of Tn3-gamma delta hybrid genes encoding chimeric proteins in the N-terminal segments of the transposases (amino acid position 1 to 242 of Tn3 or 1' to 243' of gamma delta), which has been previously shown to be responsible for specific binding of transposase to IR sequences in Tn3. Examination of their DNA-binding activities revealed that the subsegment of the N-terminus from amino acid position 1 to 109 determines the specificity of binding to the IR sequences. The third coding frame found in gamma delta, tnpX, is located downstream of tnpR and is expressed from the tnpR promoter in the absence of the tnpR gene product, resolvase/repressor, to produce a protein that inhibits the growth of the host cells. Possible roles of this protein are discussed.
为了分析决定Tn3转座酶与末端反向重复序列(IR)结合特异性的区域,我们首先确定了一个Tn3家族转座子γδ的核苷酸序列,该转座子被认为编码一种与Tn3转座酶相似的转座酶。γδ长度为5981 bp,包含三个编码框:两个是基因tnpA和tnpR,分别编码转座酶(1002个氨基酸)和解离酶/阻遏蛋白(183个氨基酸),第三个名为tnpX,编码一种功能未知但含有两个NTP结合基序的蛋白质(698个氨基酸)。然后,利用tnpA序列,我们构建了一系列Tn3-γδ杂交基因,这些基因在转座酶的N端片段(Tn3的氨基酸位置1至242或γδ的1'至243')编码嵌合蛋白,先前已证明该片段负责转座酶与Tn3中IR序列的特异性结合。对它们的DNA结合活性的检测表明,N端从氨基酸位置1至109的亚片段决定了与IR序列结合的特异性。在γδ中发现的第三个编码框tnpX位于tnpR的下游,在没有tnpR基因产物解离酶/阻遏蛋白的情况下,从tnpR启动子表达,产生一种抑制宿主细胞生长的蛋白质。本文讨论了这种蛋白质可能的作用。