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转录组分析揭示了长绒棉和短绒棉(Gossypium hirsutum L.)纤维起始和伸长机制的差异。

Transcriptome analysis reveals differences in the mechanisms of fiber initiation and elongation between long- and short-fiber cotton (Gossypium hirsutum L.) lines.

机构信息

State Key Laboratory of Cotton Biology, Institute of Cotton Research, Chinese Academy of Agricultural Science, Anyang, 455000, China.

出版信息

BMC Genomics. 2019 Aug 5;20(1):633. doi: 10.1186/s12864-019-5986-5.

Abstract

BACKGROUND

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

提高陆地棉的产量和纤维品质是棉花育种者的目标。然而,提高棉花纤维的产量和品质变得越来越紧迫。随着人口的增长,人类需要更多的棉花纤维,气候变化正在减少棉花种植的土地面积,或者使得难以确保以最佳数量获得水和其他资源。提高产量和品质的最合理手段是了解和操纵相关基因。在这里,我们使用比较转录组学来探索长纤维和短纤维棉花品系之间的基因表达差异,以鉴定对棉花改良有用的候选基因。

结果

光镜和电镜观察表明,我们的短纤维组(SFG)的初始纤维密度明显大于我们的长纤维组(LFG)。与 SFG 纤维相比,LFG 纤维在所有发育阶段都更长。比较 LFG 和 SFG 转录组揭示了总共 3538 个差异表达基因(DEGs)。值得注意的是,在所检查的所有三个发育阶段,都鉴定出两种表达模式,即一致下调(图谱 0)和一致上调(图谱 7),并且这两种模式在 SFG 和 LFG 中均显著富集。在图谱 0 中检测到 22 个已知参与纤维起始的 DEG,而在图谱 7 中检测到 31 个参与纤维伸长的 DEG。功能注释表明,这些 DEG 包括 ERF1、TUA2、TUB1 和 PER64,通过参与乙烯反应、微管合成和/或过氧化物酶(POD)催化途径,影响纤维伸长。使用 qRT-PCR 对选定基因的 RNA 测序结果进行了验证。

结论

SFG 和 LFG 转录谱的比较显示,两组之间的基因表达存在适度但重要的差异。值得注意的是,我们的结果证实了先前研究的结果,表明参与乙烯、微管和 POD 途径的基因在纤维发育中起着重要作用。22 个一致下调的纤维起始 DEG 和 31 个一致上调的纤维伸长 DEG 似乎是改良棉花纤维起始和伸长的良好候选基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e70b/6683361/cfb265adc4cf/12864_2019_5986_Fig1_HTML.jpg

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