Crénès Gwénaelle, Moundras Corinne, Demattei Marie-Véronique, Bigot Yves, Petit Agnès, Renault Sylvaine
Université François Rabelais de Tours, GICC, Parc de Grandmont, 37200 Tours, France.
Genetica. 2010 May;138(5):509-17. doi: 10.1007/s10709-009-9387-6. Epub 2009 Jul 24.
The eukaryotic transposon Mos1 is a class-II transposable element that moves using a "cut-and-paste" mechanism in which the transposase is the only protein factor required. The formation of the excision complex is well documented, but the integration step has so far received less investigation. Like all mariner-like elements, Mos1 was thought to integrate into a TA dinucleotide without displaying any other target selection preferences. We set out to synthesize what is currently known about Mos1 insertion sites, and to define the characteristics of Mos1 insertion sequences in vitro and in vivo. Statistical analysis can be used to identify the TA dinucleotides that are non-randomly targeted for transposon integration. In vitro, no specific feature determining target choice other than the requirement for a TA dinucleotide has been identified. In vivo, data were obtained from two previously reported integration hotspots: the bacterial cat gene and the Caenorhabditis elegans rDNA locus. Analysis of these insertion sites revealed a preference for TA dinucleotides that are included in TATA or TA x TA motifs, or located within AT-rich regions. Analysis of the physical properties of sequences obtained in vitro and in vivo do not help to explain Mos1 integration preferences, suggesting that other characteristics must be involved in Mos1 target choice.
真核转座子Mos1是一种II类转座元件,它通过“剪切粘贴”机制移动,其中转座酶是唯一所需的蛋白质因子。切除复合体的形成已有充分记录,但整合步骤迄今为止受到的研究较少。与所有类水手元件一样,Mos1被认为整合到TA二核苷酸中,而不表现出任何其他靶标选择偏好。我们着手综合目前已知的Mos1插入位点信息,并在体外和体内定义Mos1插入序列的特征。统计分析可用于识别非随机被转座子整合靶向的TA二核苷酸。在体外,除了对TA二核苷酸的需求外,尚未发现决定靶标选择的特定特征。在体内,数据来自两个先前报道的整合热点:细菌cat基因和秀丽隐杆线虫rDNA位点。对这些插入位点的分析揭示了对包含在TATA或TA x TA基序中或位于富含AT区域内的TA二核苷酸的偏好。对体外和体内获得的序列的物理性质分析无助于解释Mos1的整合偏好,这表明Mos1靶标选择必定涉及其他特征。