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果蝇(Drosophila subobscura)和加那利果蝇(Drosophila guanche)中成簇P因子同源物的结构与表达

Structure and expression of clustered P element homologues in Drosophila subobscura and Drosophila guanche.

作者信息

Miller W J, Paricio N, Hagemann S, Martínez-Sebastián M J, Pinsker W, de Frutos R

机构信息

Institut für Allgemeine Biologie, Abteilung Genetik, Medizinische Fakultät der Universität Wien, Austria.

出版信息

Gene. 1995 Apr 24;156(2):167-74. doi: 10.1016/0378-1119(95)00013-v.

DOI:10.1016/0378-1119(95)00013-v
PMID:7758953
Abstract

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)

摘要

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)

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Structure and expression of clustered P element homologues in Drosophila subobscura and Drosophila guanche.果蝇(Drosophila subobscura)和加那利果蝇(Drosophila guanche)中成簇P因子同源物的结构与表达
Gene. 1995 Apr 24;156(2):167-74. doi: 10.1016/0378-1119(95)00013-v.
2
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引用本文的文献

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Domesticated P elements in the Drosophila montium species subgroup have a new function related to a DNA binding property.蒙氏果蝇物种亚组中的驯化P因子具有与DNA结合特性相关的新功能。
J Mol Evol. 2005 Oct;61(4):470-80. doi: 10.1007/s00239-004-0324-0. Epub 2005 Aug 25.
2
P-Element repression in Drosophila melanogaster by a naturally occurring defective telomeric P copy.黑腹果蝇中天然存在的缺陷性端粒P拷贝对P因子的抑制作用。
Genetics. 2000 Aug;155(4):1841-54. doi: 10.1093/genetics/155.4.1841.
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DNA binding by the KP repressor protein inhibits P-element transposase activity in vitro.
KP阻遏蛋白与DNA的结合在体外抑制P因子转座酶活性。
EMBO J. 1998 Jul 15;17(14):4166-74. doi: 10.1093/emboj/17.14.4166.
4
Transposable elements as sources of variation in animals and plants.转座元件作为动植物变异的来源。
Proc Natl Acad Sci U S A. 1997 Jul 22;94(15):7704-11. doi: 10.1073/pnas.94.15.7704.
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Repeated horizontal transfer of P transposons between Scaptomyza pallida and Drosophila bifasciata.P 转座子在苍白菌潜蝇和双带果蝇之间的反复水平转移。
Genetica. 1996 Jul;98(1):43-51. doi: 10.1007/BF00120217.