期刊文献+

Glucosylceramides containing very long-acyl-chain fatty acid are critical for cotton fiber elongation by influencing brassinosteroid synthesis and signaling

在线阅读 下载PDF
导出
摘要 Sphingolipids are not only a pivotal component of membranes but also act as bioactive molecules.Cotton fiber is one of the longest plant cells and sphingolipids are closely associated with the development of cotton fiber cells.However,their function in cotton fiber cell development and its action mechanism is unclear.Through cotton genetic transformation and chemistry biological approach,we identified the function and action mechanism of the glucosylceramide synthase gene GhGCS1 and its product glucosylceramide(GluCer)in cotton fiber growth.GhGCS1 was preferentially expressed at the stage of fiber elongation and localized in the endoplasmic reticulum.Overexpression of GhGCS1 promoted GluCer synthesis and fiber elongation,which was consistent with the exogenous application of GluCer(FA-C22)(containing very long-acyl-chain fatty acid)to cotton fiber in ovule culture system in vitro.Contrarily,suppressing GhGCS1 expression inhibited GluCer synthesis and fiber elongation,which was similar as the exogenous application of GluCer synthesis inhibitor,PDMP.Transcriptome analysis revealed that the fiber elongation regulated by GhGCS1 was associated with brassinosteroid(BR)synthesis and signaling related gene expression.Meanwhile,we detected the BL content of control and transgenic fiber cells.The BL content significantly increased and decreased in up-and down-regulated transgenic fibers when compared with control fibers,respectively.Furthermore,we found that PDMP treatment blocked BR synthesis and signal transduction,while exogenous application of GluCer could enhance BR synthesis and signaling.Overall,our results revealed that GhGCS1 and GluCer regulated cotton fiber elongation by influencing BR synthesis and signaling.Our study shed a novel insight on regulatory mechanism of cotton fiber elongation and provides theoretical support,genetic resources and novel transgenic materials for improvement of crop quality.
出处 《The Crop Journal》 2025年第4期1081-1092,共12页 作物学报(英文版)
基金 funded by the National Natural Science Foundation of China(32372114,31971984) the Special Fund for Youth Team of the Southwest Universities(SWU-XJPY202306) the Chongqing Graduate Scientific Research Innovation Project(CYS23239) the Genetically Modified Organisms Breeding Major Project of China(2018ZX0800921B)。
  • 相关文献

参考文献4

二级参考文献86

  • 1Arkhipov, A., Shan, Y., Das, R., Endres, N.F., Eastwood, M.P., Wemmer, D.E., Kuriyan, J., and Shaw, D.E. (2013). Architecture and membrane interactions of the EGF receptor. Cell 152:557-569.
  • 2Bacia, K., Kim, S.A., and Schwille, P. (2006). Fluorescence cross- correlation spectroscopy in living cells. Nat. Methods 3:83-89.
  • 3Baisa, G., Mayers, J.R., and Bednarek, S.Y. (2013). Budding and braking news about clathrin-mediated endocytosis. Curr. Opin. Plant Biol. 16:718-725.
  • 4Banbury, D.N., Oakley, J.D., Sessions, R.B., and Banting, G. (2003). Tyrphostin A23 inhibits internalization of the transferrin receptor by perturbing the interaction between tyrosine motifs and the medium chain subunit of the AP-2 adaptor complex. J. Biol. Chem. 278: 12022-12028.
  • 5Bolte, S., and Cordelieres, F.P. (2006). A guided tour into subcellular colocalization analysis in light microscopy. J. Microsc. 224:213-232.
  • 6Borner, G.H., Sherrier, D.J., Weimar, T., Michselson, L.V., Hawkins, N.D., Macaskill, A., Napier, J.A., Beale, M.H., Lilley, K.S., and Dupree, P. (2005). Analysis of detergent-resistant membranes inArabidopsis. Evidence for plasma membrane lipid rafts. Plant Physiol. 137:104-116.
  • 7B(icherl, C.A., van Esse, G.W., Kruis, A., Luchtenberg, J., Westphal, A.H., Aker, J., van Hoek, A., Albrecht, C., Borst, J.W., and de Vries, S.C. (2013). Visualization of BRI1 and BAKI(SERK3) membrane receptor hetero-oligomers during brassinosteroid signaling. Plant Physiol. 162:1911-1925.
  • 8Chen, J., and Irudayaraj, J. (2010). Fluorescence lifetime cross correlation spectroscopy resolves EGFR and antagonist interaction in live cells. Anal. Chem. 82:6415-6421.
  • 9Cho, M.R., Knowles, D.W., Smith, B.L., Moulds, J.J., Agre, P., Mohandas, N., and Golan, D.E. (1999). Membrane dynamics of the water transport protein aquaporin-1 in intact human red cells. Biophye. J. 76:1136-1144.
  • 10Chung, I., Akita, R., Vandlen, R., Toomre, D., Schlessinger, J., and Mellman, I. (2010). Spatial control of EGF receptor activation by reversible dimerization on living cells. Nature 464:783-787.

共引文献29

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部