首页> 美国卫生研究院文献>Journal of Experimental Botany >A disulfide bond A-like oxidoreductase is a strong candidate gene for self-incompatibility in apricot (Prunus armeniaca) pollen
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A disulfide bond A-like oxidoreductase is a strong candidate gene for self-incompatibility in apricot (Prunus armeniaca) pollen

机译:二硫键A样氧化还原酶是杏(Prunus armeniaca)花粉中自交不亲和的强候选基因

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摘要

S-RNase based gametophytic self-incompatibility (SI) is a widespread prezygotic reproductive barrier in flowering plants. In the Solanaceae, Plantaginaceae and Rosaceae gametophytic SI is controlled by the pistil-specific S-RNases and the pollen S-locus F-box proteins but non-S-specific factors, namely modifiers, are also required. In apricot, Prunus armeniaca (Rosaceae), we previously mapped two pollen-part mutations that confer self-compatibility in cultivars Canino and Katy at the distal end of chromosome 3 (M-locus) unlinked to the S-locus. Here, we used high-resolution mapping to identify the M-locus with an ~134 kb segment containing ParM-1–16 genes. Gene expression analysis identified four genes preferentially expressed in anthers as modifier gene candidates, ParM-6, -7, -9 and -14. Variant calling of WGS Illumina data from Canino, Katy, and 10 self-incompatible cultivars detected a 358 bp miniature inverted-repeat transposable element (MITE) insertion in ParM-7 shared only by self-compatible apricots, supporting ParM-7 as strong candidate gene required for SI. ParM-7 encodes a disulfide bond A-like oxidoreductase protein, which we named ParMDO. The MITE insertion truncates the ParMDO ORF and produces a loss of SI function, suggesting that pollen rejection in Prunus is dependent on redox regulation. Based on phylogentic analyses we also suggest that ParMDO may have originated from a tandem duplication followed by subfunctionalization and pollen-specific expression.
机译:基于S-RNase的配子体自我不相容性(SI)是开花植物中广泛的合子生殖生殖屏障。在茄科中,车前草科和蔷薇科的配子体SI受雌蕊特异性S-RNase和花粉S-场所F-box蛋白的控制,但是还需要非S特异性因子,即修饰子。在杏,杏子(蔷薇科)中,我们先前绘制了两个花粉部分突变,这些突变赋予了品种Canino和Katy 3号染色体远端(M-基因座)与S-基因座不相关的自溶性。在这里,我们使用高分辨率作图来鉴定带有ParM-1-16基因的〜134 kb片段的M位点。基因表达分析确定了优先在花药中表达的四个基因,作为修饰基因候选物ParM-6,-7,-9和-14。来自Canino,Katy和10个自身不相容品种的WGS Illumina数据的变异调用在ParM-7中检测到358 bp的微型反向重复转座因子(MITE)插入,仅由自我相容的杏子共享,支持ParM-7作为强候选人SI所需的基因。 ParM-7编码一个二硫键A样氧化还原酶蛋白,我们将其命名为ParMDO。 MITE插入会截断 ParMDO ORF并导致SI功能丧失,表明 Prunus 中的花粉排斥取决于氧化还原调节。根据系统发育分析,我们还建议 ParMDO 可能是由串联复制,亚功能化和花粉特异性表达引起的。

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