TY - JOUR
T1 - Proteomic evaluation of wound-healing processes in potato (Solanum tuberosum L.) tuber tissue
AU - Chaves, Ines Maria
AU - Pinheiro, Carla Maria
AU - Caldeira Pinto Paiva, Jorge Almiro Barcelo
AU - Planchon, Sebastien
AU - Sergeant, Kjell
AU - Graça, José
AU - Costa, Gonçalo
AU - Coelho, Ana Maria
AU - Ricardo, C. P.
N1 - Ricardo, CPP (autor do ITQB)
Costa G (autor do ITQB)
PY - 2009/1/1
Y1 - 2009/1/1
N2 - Proteins from potato (Solanum tuberosum L.) tuber slices, related to the wound-healing process, were separated by 2-DE and identified by an MS analysis in MS and MS/MS mode. Slicing triggered differentiation processes that lead to changes in metabolism, activation of defence and cell-wall reinforcement. Proteins related to storage, cell growth and division, cell structure, signal transduction, energy production, disease/defence mechanisms and secondary metabolism were detected. Image analysis of the 2-DE gels revealed a time-dependent change in the complexity of the polypeptide patterns. By microscopic observation the polyalyphatic domain of suberin was dearly visible by D4, indicating that a dosing layer (primary suberisation) was formed by then. A PCA of the six sampling dates revealed two time phases, D0-D2 and D4-D8, with a border position between D2 and D4. Moreover, a PCA of differentially expressed proteins indicated the existence of a succession of proteomic events leading to wound-periderm reconstruction. Some late-expressed proteins (D6-D8), including a suberisation-associated anionic peroxidase, have also been identified in the native periderm. Despite this, protein patterns of D8 slices and native periderm were still different, suggesting that the processes of wound-periderm formation are extended in time and not fully equivalent. The information presented in this study gives dues for further work on wound healing-periderm formation processes.
AB - Proteins from potato (Solanum tuberosum L.) tuber slices, related to the wound-healing process, were separated by 2-DE and identified by an MS analysis in MS and MS/MS mode. Slicing triggered differentiation processes that lead to changes in metabolism, activation of defence and cell-wall reinforcement. Proteins related to storage, cell growth and division, cell structure, signal transduction, energy production, disease/defence mechanisms and secondary metabolism were detected. Image analysis of the 2-DE gels revealed a time-dependent change in the complexity of the polypeptide patterns. By microscopic observation the polyalyphatic domain of suberin was dearly visible by D4, indicating that a dosing layer (primary suberisation) was formed by then. A PCA of the six sampling dates revealed two time phases, D0-D2 and D4-D8, with a border position between D2 and D4. Moreover, a PCA of differentially expressed proteins indicated the existence of a succession of proteomic events leading to wound-periderm reconstruction. Some late-expressed proteins (D6-D8), including a suberisation-associated anionic peroxidase, have also been identified in the native periderm. Despite this, protein patterns of D8 slices and native periderm were still different, suggesting that the processes of wound-periderm formation are extended in time and not fully equivalent. The information presented in this study gives dues for further work on wound healing-periderm formation processes.
KW - DEFENSE-RELATED PROTEINS
KW - PLANTS
KW - PROTEASE INHIBITORS
KW - CELL-DEATH
KW - SUBERIZATION
KW - DIHYDROFLAVONOL-4-REDUCTASE
KW - SUBERIN
KW - MEDICAGO-TRUNCATULA
KW - SIGNAL-TRANSDUCTION
KW - OXIDATIVE STRESS
U2 - 10.1002/pmic.200700649
DO - 10.1002/pmic.200700649
M3 - Article
SN - 1615-9853
VL - 9
SP - 4154
EP - 4175
JO - Proteomics
JF - Proteomics
IS - 17
ER -