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首页> 外文期刊>Theoretical and Applied Genetics >Annotation of a 95-kb Populus deltoides genomic sequence reveals a disease resistance gene cluster and novel class I and class II transposable elements
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Annotation of a 95-kb Populus deltoides genomic sequence reveals a disease resistance gene cluster and novel class I and class II transposable elements

机译:95kb的胡杨(Populus deltoides)基因组序列的注释揭示了抗病基因簇和新颖的I类和II类转座因子

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摘要

Poplar has become a model system for functional genomics in woody plants. Here, we report the sequencing and annotation of the first large contiguous stretch of genomic sequence (95 kb) of poplar, corresponding to a bacterial artificial chromosome clone mapped 0.6 centiMorgan from the Melampsora larici-populina resistance locus. The annotation revealed 15 putative genetic objects, of which five were classified as hypothetical genes that were similar only with expressed sequence tags from poplar. Ten putative objects showed similarity with known genes, of which one was similar to a kinase. Three other objects corresponded to the toll/interleukin-1 receptorucleotide-binding site/leucine-rich repeat class of plant disease resistance genes, of which two were predicted to encode an amino terminal nuclear localization signal. Four objects were homologous to the Ty1/copia family of class I transposable elements, one of which was designated Retropop and interrupted one of the disease resistance genes. Two other objects constituted a novel Spm-like class II transposable element, which we designated Magali.
机译:杨树已成为木本植物功能基因组学的模型系统。在这里,我们报道了杨树基因组序列的第一个大的连续延伸序列(95 kb)的测序和注释,该序列对应于一个细菌人工染色体克隆,该克隆从Melampsora larici-populina抗性基因座映射了0.6 centiMorgan。注释揭示了15个推定的遗传对象,其中有5个被归类为假设基因,仅与白杨表达的序列标签相似。十个推定的对象显示与已知基因的相似性,其中一个与激酶相似。其他三个对象对应于植物病害抗性基因的toll / interleukin-1受体/核苷酸结合位点/富含亮氨酸的重复类,其中两个对象预计会编码氨基末端核定位信号。四个物体与I类转座子的Ty1 / copia家族同源,其中一个被命名为Retropop并打断了一种抗病基因。另外两个物体构成了一种新颖的类Spm的II类转座因子,我们将其命名为Magali。

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  • 来源
    《Theoretical and Applied Genetics》 |2004年第1期|10-22|共13页
  • 作者单位

    Department of Plant Systems Biology Flanders Interuniversity Institute for Biotechnology Ghent UniversityCIRAD-Biotrop TA40/03;

    Department of Plant Systems Biology Flanders Interuniversity Institute for Biotechnology Ghent University;

    Department of Plant Systems Biology Flanders Interuniversity Institute for Biotechnology Ghent University;

    Department of Plant Systems Biology Flanders Interuniversity Institute for Biotechnology Ghent UniversityUnité de Recherche en Génomique Végétale INRA;

    Department of Plant Systems Biology Flanders Interuniversity Institute for Biotechnology Ghent UniversityLaboratoire de Biologie Vasculaire Institut de Pharmacologie et Biologie Structurale;

    Department of Plant Physiology University of Umeå;

    Department of Plant Systems Biology Flanders Interuniversity Institute for Biotechnology Ghent UniversityLaboratoire Associé de l’Institut National de la Recherche Agronomique (France) Ghent University;

    Department of Plant Systems Biology Flanders Interuniversity Institute for Biotechnology Ghent University;

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