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首页> 外文期刊>BMC Genomics >Transcriptome analysis reveals differences in the mechanisms of fiber initiation and elongation between long- and short-fiber cotton ( Gossypium hirsutum L.) lines
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Transcriptome analysis reveals differences in the mechanisms of fiber initiation and elongation between long- and short-fiber cotton ( Gossypium hirsutum L.) lines

机译:转录组分析揭示了长纤维和短纤维棉(Gossypium hirsutum L.)品系之间纤维萌生和伸长机制的差异

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摘要

Improving the yield and fiber quality of upland cotton is a goal of plant breeders. However, increasing the yield and quality of cotton fibers is becoming more urgent. While the growing human population needs more cotton fiber, climate change is reducing the amount of land on which cotton can be planted, or making it difficult to ensure that water and other resources will be available in optimal quantities. The most logical means of improving yield and quality is understanding and manipulating the genes involved. Here, we used comparative transcriptomics to explore differences in gene expression between long- and short-fiber cotton lines to identify candidate genes useful for cotton improvement. Light and electron microscopy revealed that the initial fiber density was significantly greater in our short-fiber group (SFG) than in our long-fiber group (LFG). Compared with the SFG fibers, the LFG fibers were longer at all developmental stages. Comparison of the LFG and SFG transcriptomes revealed a total of 3538 differentially expressed genes (DEGs). Notably, at all three developmental stages examined, two expression patterns, consistently downregulated (profile?0) and consistently upregulated (profile?7), were identified, and both were significantly enriched in the SFG and LFG. Twenty-two DEGs known to be involved in fiber initiation were detected in profile?0, while 31 DEGs involved in fiber elongation were detected in profile?7. Functional annotation suggested that these DEGs, which included ERF1, TUA2, TUB1, and PER64, affect fiber elongation by participating in the ethylene response, microtubule synthesis, and/or the peroxidase (POD) catalytic pathway. qRT-PCR was used to confirm the RNA sequencing results for select genes. A comparison of SFG and LFG transcription profiles revealed modest but important differences in gene expression between the groups. Notably, our results confirm those of previous studies suggesting that genes involved in ethylene, tubulin, and POD pathways play important roles in fiber development. The 22 consistently downregulated DEGs involved in fiber initiation and the 31 consistently upregulated genes involved in fiber elongation are seemingly good candidate genes for improving fiber initiation and elongation in cotton.
机译:提高陆地棉的产量和纤维质量是植物育种者的目标。但是,提高棉纤维的产量和质量变得更加紧迫。尽管不断增长的人口需要更多的棉纤维,但气候变化正在减少可种植棉花的土地数量,或者使确保水和其他资源的最佳供应量变得困难。提高产量和质量的最合乎逻辑的方法是了解和操纵涉及的基因。在这里,我们使用比较转录组学来研究长纤维和短纤维棉花品系之间基因表达的差异,以确定可用于棉花改良的候选基因。光学和电子显微镜显示,短纤维组(SFG)的初始纤维密度显着大于长纤维组(LFG)的初始纤维密度。与SFG纤维相比,LFG纤维在所有发育阶段都更长。 LFG和SFG转录组的比较显示共有3538个差异表达基因(DEG)。值得注意的是,在所研究的所有三个发育阶段中,均鉴定出了两种表达模式,即持续下调(profile?0)和持续上调(profile?7),并且两种表达模式均在SFG和LFG中显着富集。在轮廓α0中检测到22个已知与纤维起始有关的DEG,在轮廓α7中检测到31个与纤维伸长相关的DEG。功能注释表明,这些DEG(包括ERF1,TUA2,TUB1和PER64)通过参与乙烯响应,微管合成和/或过氧化物酶(POD)催化途径来影响纤维伸长。使用qRT-PCR确认所选基因的RNA测序结果。 SFG和LFG转录图谱的比较揭示了两组之间基因表达的适度但重要的差异。值得注意的是,我们的结果证实了先前的研究结果,表明与乙烯,微管蛋白和POD途径有关的基因在纤维发育中起重要作用。与纤维萌发有关的22个DEGs持续下调,而与纤维伸长有关的31个DEGs上调基因似乎是改善棉花纤维萌发和伸长的良好候选基因。

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