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Regions outside of the Leucine-Rich Repeats of Flax Rust Resistance Proteins Play a Role in Specificity Determination

机译:亚麻抗锈蛋白富亮氨酸重复序列以外的区域在特异性测定中起作用

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摘要

Multiple alleles controlling different gene-for-gene flax rust resistance specificities occur at the L locus of flax. At least three distinct regions can be recognized in the predicted protein products: the Toll/interleukin-1 receptor homology (TIR) region, a nucleotide binding site (NBS) region, and a leucine-rich repeat (LRR) region. Replacement of the TIR-encoding region of the L6 allele with the corresponding regions of L2 or LH by recombination changed the specificity of the allele from L6 to L7. Replacement of the TIR and most of the NBS-encoding region of L10 with the equivalent region of L2 or L9 generated recombinant alleles having a novel specificity. However, replacement of the L10 TIR-encoding region with the TIR-encoding region of L2 gave rise to an allele with no detectable specificity. These data indicate that non-LRR regions can determine specificity differences between allelic gene products and that functional specificity involves interactions between coadapted polymorphic regions in the protein products of the alleles. Evidence for the action of diversifying selection on the TIR region is observed.
机译:控制亚麻基因L位点的多个等位基因控制着不同的基因对基因的亚麻锈病抗性特异性。可以在预测的蛋白质产物中识别至少三个不同的区域:Toll /白介素-1受体同源性(TIR)区,核苷酸结合位点(NBS)区和富含亮氨酸的重复序列(LRR)区。通过重组用L2或LH的相应区域替换L6等位基因的TIR编码区,使等位基因的特异性从L6变为L7。用L2或L9的等效区域替换L10的TIR和大多数NBS编码区域,产生具有新颖特异性的重组等位基因。但是,用L2的TIR编码区替换L10 TIR编码区会产生等位基因,且检测不到特异性。这些数据表明,非LRR区可以确定等位基因产物之间的特异性差异,并且功能特异性涉及等位基因蛋白产物中共适应的多态性区域之间的相互作用。观察到在TIR区域进行多样化选择的作用的证据。

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