日本蜜蜂(膜翅目,细腰亚目)中类水手元件Acmar1的克隆与特性分析
Cloning and characterization of Acmar1, a mariner-like element in the asiatic honey bee, Apis cerana japonica (Hymenoptera, Apocrita).
作者信息
Sumitani Megumi, Lee Jae Min, Hatakeyama Masatsugu, Oishi Kugao
机构信息
Division of Bioscience, Graduate School of Science and Technology, Kobe University, Nada, Kobe, Japan.
出版信息
Arch Insect Biochem Physiol. 2002 Aug;50(4):183-90. doi: 10.1002/arch.10043.
A mariner-like element was cloned from the genome of the Asiatic honey bee, Apis cerana japonica (Hymenoptera, Apocrita). The (composite) clone, named Acmar1, was 1,378 bp long, and encoded 336 amino acids corresponding to a transposase-like putative polypeptide in a single open reading frame. The D,D(34)D motif, the catalytic domain of the mariner transposase, was present, although there was a deletion of five amino acid residues within it as compared with the active transposase in Drosophila mauritiana. Nineteen-bp-long imperfect inverted terminal repeat-like sequences flanked by TA dinucleotides, the typical target site for mariner insertion, were observed. Southern blot analysis using a fragment covering two-thirds of the Acmar1 transposase coding sequence as a probe indicated the presence of multiple Acmar1-like elements in the genome. Maximum-parsimony phylogenetic analysis based on the transposase amino acid sequences of insect mariner-like elements revealed that Acmar1 is a member of the mellifera subfamily.
从日本蜜蜂(膜翅目,细腰亚目)的基因组中克隆出一种类水手元件。这个(复合)克隆名为Acmar1,长度为1378 bp,在一个单一的开放阅读框中编码336个氨基酸,对应一种类转座酶的假定多肽。虽然与毛里求斯果蝇中的活性转座酶相比,其内部有五个氨基酸残基缺失,但仍存在水手转座酶的催化结构域D,D(34)D基序。观察到由TA二核苷酸侧翼的19 bp长的不完全反向末端重复样序列,这是水手插入的典型靶位点。使用覆盖Acmar1转座酶编码序列三分之二的片段作为探针进行Southern印迹分析表明,基因组中存在多个Acmar1样元件。基于昆虫类水手元件转座酶氨基酸序列的最大简约系统发育分析表明,Acmar1是蜜蜂亚科的一个成员。