Identification of Diverse Stress-Responsive Xylem Sap Peptides in Soybean

Int J Mol Sci. 2022 Aug 3;23(15):8641. doi: 10.3390/ijms23158641.

Abstract

Increasing evidence has revealed that plant secretory peptides are involved in the long-distance signaling pathways that help to regulate plant development and signal stress responses. In this study, we purified small peptides from soybean (Glycine max) xylem sap via o-chlorophenol extraction and conducted an in-depth peptidomic analysis using a mass spectrometry (MS) and bioinformatics approach. We successfully identified 14 post-translationally modified peptide groups belonging to the peptide families CEP (C-terminally encoded peptides), CLE (CLAVATA3/embryo surrounding region-related), PSY (plant peptides containing tyrosine sulfation), and XAP (xylem sap-associated peptides). Quantitative PCR (qPCR) analysis showed unique tissue expression patterns among the peptide-encoding genes. Further qPCR analysis of some of the peptide-encoding genes showed differential stress-response profiles toward various abiotic stress factors. Targeted MS-based quantification of the nitrogen deficiency-responsive peptides, GmXAP6a and GmCEP-XSP1, demonstrated upregulation of peptide translocation in xylem sap under nitrogen-deficiency stress. Quantitative proteomic analysis of GmCEP-XSP1 overexpression in hairy soybean roots revealed that GmCEP-XSP1 significantly impacts stress response-related proteins. This study provides new insights that root-to-shoot peptide signaling plays important roles in regulating plant stress-response mechanisms.

Keywords: C-terminally encoded peptide; CLV3/ESR-related; long-distance; peptide signaling; peptidomic; post-translational modification; root-to-shoot; sulfated peptide; xylem sap.

MeSH terms

  • Glycine max* / genetics
  • Glycine max* / metabolism
  • Humans
  • Nitrogen / metabolism
  • Peptides / metabolism
  • Plant Proteins / metabolism
  • Plant Roots / metabolism
  • Proteomics*
  • Xylem / metabolism

Substances

  • Peptides
  • Plant Proteins
  • Nitrogen