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Characterization of Non-heading Mutation in Heading Chinese Cabbage (Brassica rapa L. ssp. pekinensis)

机译:大白菜(Brassica rapa L. ssp。pekinensis)的非抽穗突变特征

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摘要

Heading is a key agronomic trait of Chinese cabbage. A non-heading mutant with flat growth of heading leaves (fg-1) was isolated from an EMS-induced mutant population of the heading Chinese cabbage inbred line A03. In fg-1 mutant plants, the heading leaves are flat similar to rosette leaves. The epidermal cells on the adaxial surface of these leaves are significantly smaller, while those on the abaxial surface are much larger than in A03 plants. The segregation of the heading phenotype in the F2 and BC1 population suggests that the mutant trait is controlled by a pair of recessive alleles. Phytohormone analysis at the early heading stage showed significant decreases in IAA, ABA, JA and SA, with increases in methyl IAA and trans-Zeatin levels, suggesting they may coordinate leaf adaxial-abaxial polarity, development and morphology in fg-1. RNA-sequencing analysis at the early heading stage showed a decrease in expression levels of several auxin transport (BrAUX1, BrLAXs, and BrPINs) and responsive genes. Transcript levels of important ABA responsive genes, including BrABF3, were up-regulated in mid-leaf sections suggesting that both auxin and ABA signaling pathways play important roles in regulating leaf heading. In addition, a significant reduction in BrIAMT1 transcripts in fg-1 might contribute to leaf epinastic growth. The expression profiles of 19 genes with known roles in leaf polarity were significantly different in fg-1 leaves compared to wild type, suggesting that these genes might also regulate leaf heading in Chinese cabbage. In conclusion, leaf heading in Chinese cabbage is controlled through a complex network of hormone signaling and abaxial-adaxial patterning pathways. These findings increase our understanding of the molecular basis of head formation in Chinese cabbage.
机译:抽穗是大白菜的关键农艺性状。从EMS诱导的抽穗大白菜自交系A03的突变群体中分离出抽穗叶片(fg-1)生长平坦的非抽穗突变体。在fg-1突变植物中,抽穗叶是扁平的,类似于莲座叶。这些叶片的近轴表面上的表皮细胞明显较小,而远轴表面上的表皮细胞则比A03植物大得多。 F2和BC1群体中的标题表型分离表明该突变性状是由一对隐性等位基因控制的。抽穗初期的植物激素分析表明,IAA,ABA,JA和SA的含量显着降低,甲基IAA和反式玉米素水平升高,表明它们可能与fg-1的叶片前后轴极性,发育和形态协调一致。在抽穗初期,RNA测序分析表明几种生长素转运蛋白(BrAUX1,BrLAX和BrPIN)和响应基因的表达水平下降。重要的ABA响应基因,包括BrABF3,的转录水平在中叶切片中被上调,表明生长素和ABA信号通路均在调节叶的抽穗中起重要作用。此外,fg-1中BrIAMT1转录物的显着减少可能有助于叶片的表观生长。与野生型相比,fg-1叶片中19个在叶片极性中具有已知作用的基因的表达谱有显着差异,这表明这些基因也可能调节大白菜的叶片抽穗。总之,大白菜的叶片抽穗是通过激素信号传导和背面-轴向构图途径的复杂网络来控制的。这些发现增加了我们对大白菜头部形成的分子基础的理解。

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