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一种神经酰胺合酶基因的过表达通过促进含有二羟基长链碱基和极长链脂肪酸的神经酰胺的合成来抑制纤维细胞的起始和伸长。

Overexpression of a ceramide synthase gene,, inhibits fiber cell initiation and elongation by promoting the synthesis of ceramides containing dihydroxy LCB and VLCFA.

作者信息

Li Guiming, Wang Qiaoling, Meng Qian, Wang Guanhua, Xu Fan, Chen Qian, Liu Fang, Hu Yulin, Luo Ming

机构信息

Key Laboratory of Biotechnology and Crop Quality Improvement, Ministry of Agriculture/Biotechnology Research Center, Southwest University, Chongqing, China.

Key Laboratory of Horticulture Science for Southern Mountains Regions of Ministry of Education, College of Horticulture and Landscape Architecture, Southwest University, Chongqing, China.

出版信息

Front Plant Sci. 2022 Sep 2;13:1000348. doi: 10.3389/fpls.2022.1000348. eCollection 2022.

DOI:10.3389/fpls.2022.1000348
PMID:36119591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9478514/
Abstract

Cotton is an important natural fiber crop worldwide. Cotton fiber cell is regarded as an ideal material for studying the growth and development of plant cells. Sphingolipids are important components of biomembrane and bioactive molecules which participate in many processes such as plant growth, development regulation, stimulus sensing, and stress response. However, the functions of sphingolipids in the cotton fiber development are still unclear. In the present study, we identified a cotton ceramide synthase gene, , which is predominantly expressed in fiber cell. The GhCS1 is located in the endoplasmic reticulum and has the conserved domains of ceramide synthase. Overexpression of gene inhibited both vegetative and reproductive growth in cotton. Importantly, the fiber cell initiation and elongation were severely inhibited when compared with control. Comparison of the sphingolipid profile in the 0-DPA (days past anthesis) ovule (with fiber cell) between control and transgenic cotton plants showed that the content of sphingosines (Sph) decreased significantly in transgenic ovules, whereas the content of phyto-sphingosines (Phyto-Sph) had no change. Meanwhile, the content of ceramide containing Sph and very-long-chain fatty acid (VLCFA) increased significantly in transgenic ovules, while ceramide containing Phyto-Sph and long-chain fatty acids (LCFA)/VLCFA significantly decreased. These results indicated that was a functional ceramide synthase, which preferentially used Sph and VLCFA as substrates and was different from the ceramide synthase AtLOH1AtLOH3, which preferentially used Phyto-Sph and VLCFA as substrates, and also different from AtLOH2, which preferentially used Sph and LCFA as substrates. It is suggested that might be a new ceramide synthase gene in the plant, play some roles in the development of fiber cells and cotton plants.

摘要

棉花是全球重要的天然纤维作物。棉纤维细胞被视为研究植物细胞生长发育的理想材料。鞘脂是生物膜的重要组成成分和生物活性分子,参与植物生长、发育调控、刺激感知及应激反应等诸多过程。然而,鞘脂在棉纤维发育中的功能仍不清楚。在本研究中,我们鉴定了一个棉花神经酰胺合酶基因,其在纤维细胞中大量表达。GhCS1定位于内质网,具有神经酰胺合酶的保守结构域。该基因的过表达抑制了棉花的营养生长和生殖生长。重要的是,与对照相比,纤维细胞的起始和伸长受到严重抑制。比较对照和转基因棉花植株0天开花后天数(DPA)胚珠(带有纤维细胞)中的鞘脂谱,发现转基因胚珠中鞘氨醇(Sph)含量显著降低,而植物鞘氨醇(Phyto-Sph)含量无变化。同时,含有Sph和超长链脂肪酸(VLCFA)的神经酰胺在转基因胚珠中显著增加,而含有Phyto-Sph和长链脂肪酸(LCFA)/VLCFA的神经酰胺显著降低。这些结果表明,该基因是一个功能性神经酰胺合酶,优先使用Sph和VLCFA作为底物,与优先使用Phyto-Sph和VLCFA作为底物的神经酰胺合酶AtLOH1和AtLOH3不同,也与优先使用Sph和LCFA作为底物的AtLOH2不同。推测该基因可能是植物中的一个新的神经酰胺合酶基因,在纤维细胞和棉花植株的发育中发挥某些作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/b7eec05fb1d1/fpls-13-1000348-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/3e2cb63a91b4/fpls-13-1000348-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/67612d8581f3/fpls-13-1000348-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/2aa29b7fa5bd/fpls-13-1000348-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/493b3273ceef/fpls-13-1000348-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/3999a611b9db/fpls-13-1000348-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/2264772cc5cc/fpls-13-1000348-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/b7eec05fb1d1/fpls-13-1000348-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/3e2cb63a91b4/fpls-13-1000348-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/67612d8581f3/fpls-13-1000348-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/2aa29b7fa5bd/fpls-13-1000348-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/493b3273ceef/fpls-13-1000348-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/3999a611b9db/fpls-13-1000348-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/2264772cc5cc/fpls-13-1000348-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ead8/9478514/b7eec05fb1d1/fpls-13-1000348-g007.jpg

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