Comparative proteomics analysis of whitetop (Lepidium draba L.) seedlings in response to exogenous glucose

Int J Biol Macromol. 2018 Dec;120(Pt B):2458-2465. doi: 10.1016/j.ijbiomac.2018.09.016. Epub 2018 Sep 5.

Abstract

In this research, a comparative proteomics approach was conducted to understand the physiological processes behind the sulforaphane formation in whitetop seedlings in response to exogenous glucose. Initially, 5-day-old whitetop seedlings were elicited by different concentrations (0, 166, 250, 277, 360 mM) of glucose for 72 h. According to the results, sulforaphane formation was influenced in a dose-dependent manner by glucose, and was maximized with the concentrations of 166 and 250 mM. Consequently, 2-dimensional gel electrophoresis was performed on the 166 mM glucose-elicited seedlings and it was shown that 25 protein spots were differentially expressed between glucose-elicited seedlings and control. Two hypothetical (were down-regulated) and 9 unique proteins (44% and 56% up- and down-regulated, respectively) were identified based on the Mass spectrometry analysis. According to the functional classification of the unique proteins, photosynthetic, chaperone, energy metabolism, signaling and sorting related proteins are marked in response to the glucose elicitation. This is the first report to successfully identify the Abscisic acid receptor PYR1-like and sorting nexin 1 isoform X1 by proteomics technique. In addition, the role of the sorting nexin 1 isoform X1 in the glucose-elicited whitetop seedling is reported for the first time.

Keywords: Lepidium draba; Proteomics; Sulforaphane; Two-Dimensional Gel Electrophoresis.

Publication types

  • Comparative Study

MeSH terms

  • Dose-Response Relationship, Drug
  • Gene Expression Regulation, Plant / drug effects
  • Glucose / pharmacology*
  • Lepidium / cytology
  • Lepidium / drug effects*
  • Lepidium / genetics
  • Lepidium / metabolism*
  • Proteomics*
  • Seedlings / drug effects*
  • Seedlings / metabolism*
  • Signal Transduction / drug effects
  • Time Factors

Substances

  • Glucose