Miller W J, Paricio N, Hagemann S, Martínez-Sebastián M J, Pinsker W, de Frutos R
Institut für Allgemeine Biologie, Abteilung Genetik, Medizinische Fakultät der Universität Wien, Austria.
Gene. 1995 Apr 24;156(2):167-74. doi: 10.1016/0378-1119(95)00013-v.
Sequence relationships and functional aspects were analysed in the P element homologues of Drosophila subobscura (Ds) and D. guanche (Dg). In both species, the P homologues are clustered at a single genomic position. They lack the characteristic terminal structures of actively transposing P elements, but they have the coding capacity for a 66-kDa 'repressor-like' protein. Two different types of cluster units (G-type and A-type) can be distinguished. The A-type unit, which is present in multiple copies, is transcribed in adult flies. In contrast, the G-type unit has a much lower copy number and is apparently not expressed. In Dg, the isolated G-type sequence carries a 420-bp insertion in the promoter region, which is probably responsible for inactivation. Sequence comparisons of different cluster units show that differentiation of the two types precedes the lineage split of these species. Substitution rates of the deduced proteins reveal two distinct subregions: high variability at the N terminus and strong sequence conservation in the rest of the protein. The variable region contains motifs characteristic of DNA-binding proteins. Adaptive diversification of the cluster units towards specific binding properties might be a plausible explanation for variability in the N-termini. Both unit types have lost the weak promoter region characteristic of P transposons. In the A-type unit, a new promoter has been formed which is apparently composed of parts of insertion sequences derived from two different mobile elements.(ABSTRACT TRUNCATED AT 250 WORDS)
对暗果蝇(Ds)和加那利果蝇(Dg)的P元件同源物的序列关系和功能方面进行了分析。在这两个物种中,P同源物都聚集在基因组的单个位置。它们缺乏活跃转座P元件的特征性末端结构,但具有编码66 kDa“阻遏物样”蛋白的能力。可以区分出两种不同类型的簇单元(G型和A型)。多拷贝存在的A型单元在成年果蝇中被转录。相比之下,G型单元的拷贝数要低得多,且显然不表达。在Dg中,分离出的G型序列在启动子区域有一个420 bp的插入,这可能是其失活的原因。不同簇单元的序列比较表明,这两种类型的分化先于这些物种的谱系分化。推导蛋白质的替换率揭示了两个不同的亚区域:N端高度可变,蛋白质其余部分序列高度保守。可变区域包含DNA结合蛋白的特征基序。簇单元向特定结合特性的适应性多样化可能是N端变异性的一个合理的解释。两种单元类型都失去了P转座子特有的弱启动子区域。在A型单元中,形成了一个新的启动子,它显然由来自两个不同移动元件的插入序列部分组成。(摘要截短于250字)