Major Cys protease activities are not essential for senescence in individually darkened Arabidopsis leaves
Background Papain-like Cys Proteases (PLCPs) and Vacuolar Processing Enzymes (VPEs) are amongst the most highly expressed proteases during leaf senescence in Arabidopsis. Using activity-based protein profiling (ABPP), a method that enables detection of active enzymes within a complex sample using chemical probes, the activities of PLCPs and VPEs were investigated in individually darkened leaves of Arabidopsis, and their role in senescence was tested in null mutants. Results ABPP and mass spectrometry revealed an increased activity of several PLCPs, particularly RD21A and AALP. By contrast, despite increased VPE transcript levels, active VPE decreased in individually darkened leaves. Eight protease knock-out lines and two protease over expressing lines were subjected to senescence phenotype analysis to determine the importance of individual protease activities to senescence. Unexpectedly, despite the absence of dominating PLCP activities in these plants, the rubisco and chlorophyll decline in individually darkened leaves and the onset of whole plant senescence were unaltered. However, a significant delay in progression of whole plant senescence was observed in aalp-1 and rd21A-1/aalp-1 mutants, visible in the reduced number of senescent leaves. Conclusions Major Cys protease activities are not essential for dark-induced and developmental senescence and only a knock out line lacking AALP shows a slight but significant delay in plant senescence..
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2017 |
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| Erschienen: |
2017 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:17 |
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| Enthalten in: |
BMC plant biology - 17(2017), 1 vom: 06. Jan. |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Pružinská, Adriana [VerfasserIn] |
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| Links: |
Volltext [kostenfrei] |
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| Themen: |
Activity-based protein profiling |
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| Anmerkungen: |
© The Author(s). 2017 |
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| doi: |
10.1186/s12870-016-0955-5 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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SPR027304213 |
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| 245 | 1 | 0 | |a Major Cys protease activities are not essential for senescence in individually darkened Arabidopsis leaves |
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| 520 | |a Background Papain-like Cys Proteases (PLCPs) and Vacuolar Processing Enzymes (VPEs) are amongst the most highly expressed proteases during leaf senescence in Arabidopsis. Using activity-based protein profiling (ABPP), a method that enables detection of active enzymes within a complex sample using chemical probes, the activities of PLCPs and VPEs were investigated in individually darkened leaves of Arabidopsis, and their role in senescence was tested in null mutants. Results ABPP and mass spectrometry revealed an increased activity of several PLCPs, particularly RD21A and AALP. By contrast, despite increased VPE transcript levels, active VPE decreased in individually darkened leaves. Eight protease knock-out lines and two protease over expressing lines were subjected to senescence phenotype analysis to determine the importance of individual protease activities to senescence. Unexpectedly, despite the absence of dominating PLCP activities in these plants, the rubisco and chlorophyll decline in individually darkened leaves and the onset of whole plant senescence were unaltered. However, a significant delay in progression of whole plant senescence was observed in aalp-1 and rd21A-1/aalp-1 mutants, visible in the reduced number of senescent leaves. Conclusions Major Cys protease activities are not essential for dark-induced and developmental senescence and only a knock out line lacking AALP shows a slight but significant delay in plant senescence. | ||
| 650 | 4 | |a Senescence |7 (dpeaa)DE-He213 | |
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| 650 | 4 | |a Papain-like proteases |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Vacuolar processing enzymes |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Shindo, Takayuki |4 aut | |
| 700 | 1 | |a Niessen, Sherry |4 aut | |
| 700 | 1 | |a Kaschani, Farnusch |4 aut | |
| 700 | 1 | |a Tóth, Réka |4 aut | |
| 700 | 1 | |a Millar, A. Harvey |4 aut | |
| 700 | 1 | |a van der Hoorn, Renier A. L. |4 aut | |
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