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首页> 外文期刊>Frontiers in Plant Science >Quantitative Trait Transcripts Mapping Coupled with Expression Quantitative Trait Loci Mapping Reveal the Molecular Network Regulating the Apetalous Characteristic in Brassica napus L.
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Quantitative Trait Transcripts Mapping Coupled with Expression Quantitative Trait Loci Mapping Reveal the Molecular Network Regulating the Apetalous Characteristic in Brassica napus L.

机译:定量性状转录本定位与表达定量性状基因座定位相结合,揭示了调节 L.的无性状特征的分子网络。

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The apetalous trait of rapeseed ( Brassica napus , AACC, 2 n = 38) is important for breeding an ideal high-yield rapeseed with superior klendusity to Sclerotinia sclerotiorum . Currently, the molecular mechanism underlying the apetalous trait of rapeseed is unclear. In this study, 14 petal regulators genes were chosen as target genes (TGs), and the expression patterns of the 14 TGs in the AH population, containing 189 recombinant inbred lines derived from a cross between apetalous “APL01” and normal “Holly,” were analyzed in two environments using qRT-PCR. Phenotypic data of petalous degree (PDgr) in the AH population were obtained from the two environments. Both quantitative trait transcript (QTT)-association mapping and expression QTL (eQTL) analyses of TGs expression levels were performed to reveal regulatory relationships among TGs and PDgr. QTT mapping for PDgr determined that PLURIPETALA ( PLP ) was the major negative QTT associated with PDgr in both environments, suggesting that PLP negatively regulates the petal development of line “APL01.” The QTT mapping of PLP expression levels showed that CHROMATIN-REMODELING PROTEIN 11 ( CHR11 ) was positively associated with PLP expression, indicating that CHR11 acts as a positive regulator of PLP expression. Similarly, QTT mapping for the remaining TGs identified 38 QTTs, associated with 13 TGs, and 31 QTTs, associated with 10 TGs, respectively, in the first and second environments. Additionally, eQTL analyses of TG expression levels showed that 12 and 11 unconditional eQTLs were detected in the first and second environment, respectively. Based on the QTTs and unconditional eQTLs detected, we presented a hypothetical molecular regulatory network in which 14 petal regulators potentially regulated the apetalous trait in “APL01” through the CHR11-PLP pathway. PLP acts directly as the terminal signal integrator negatively regulating petal development in the CHR11-PLP pathway. These findings will aid in the understanding the molecular mechanism underlying the apetalous trait of rapeseed.
机译:油菜的无性状(甘蓝型油菜,AACC,2 n = 38)对于培育理想的高产油菜籽具有较高的菌核力对菌核菌很重要。目前,尚不清楚油菜的花瓣特性的分子机制。在这项研究中,选择了14个花瓣调控基因作为靶基因(TG),并且在AH人群中14个TG的表达模式包含了189个重组自交系,这些重组自交系来源于无花瓣的“ APL01”和正常的“冬青”。使用qRT-PCR在两种环境中进行了分析。从这两种环境中获得了AH种群中花瓣度(PDgr)的表型数据。进行了TGs表达水平的定量性状转录本(QTT)-关联作图和表达QTL(eQTL)分析,以揭示TGs和PDgr之间的调节关系。 PDgr的QTT定位图确定PLURIPETALA(PLP)是两种环境中与PDgr相关的主要负QTT值,表明PLP负调控线“ APL01”的花瓣发育。对PLP表达水平的QTT定位表明,染色质重塑蛋白11(CHR11)与PLP表达呈正相关,表明CHR11充当PLP表达的正调节剂。类似地,在第一和第二环境中,其余TG的QTT映射分别确定了38个QTT(与13个TG相关)和31个QTT(与10个TG相关)。此外,对TG表达水平的eQTL分析表明,在第一和第二环境中分别检测到12和11个无条件eQTL。基于检测到的QTT和无条件eQTL,我们提出了一个假想的分子调控网络,其中14个花瓣调控因子可能通过CHR11-PLP途径调控“ APL01”中的花瓣特性。 PLP直接充当终端信号积分器,负调控CHR11-PLP途径中的花瓣发育。这些发现将有助于理解油菜的花瓣性状的分子机制。

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