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Chlorophyll catabolism precedes changes in chloroplast structure and proteome during leaf senescence
The earliest visual changes of leaf senescence occur in the chloroplast as chlorophyll is degraded and photosynthesis declines. Yet, a comprehensive understanding of the sequence of catabolic events occurring in chloroplasts during natural leaf senescence is still missing. Here, we combined confocal...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508775/ https://www.ncbi.nlm.nih.gov/pubmed/31245770 http://dx.doi.org/10.1002/pld3.127 |
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author | Tamary, Eyal Nevo, Reinat Naveh, Leah Levin‐Zaidman, Smadar Kiss, Vladimir Savidor, Alon Levin, Yishai Eyal, Yoram Reich, Ziv Adam, Zach |
author_facet | Tamary, Eyal Nevo, Reinat Naveh, Leah Levin‐Zaidman, Smadar Kiss, Vladimir Savidor, Alon Levin, Yishai Eyal, Yoram Reich, Ziv Adam, Zach |
author_sort | Tamary, Eyal |
collection | PubMed |
description | The earliest visual changes of leaf senescence occur in the chloroplast as chlorophyll is degraded and photosynthesis declines. Yet, a comprehensive understanding of the sequence of catabolic events occurring in chloroplasts during natural leaf senescence is still missing. Here, we combined confocal and electron microscopy together with proteomics and biochemistry to follow structural and molecular changes during Arabidopsis leaf senescence. We observed that initiation of chlorophyll catabolism precedes other breakdown processes. Chloroplast size, stacking of thylakoids, and efficiency of PSII remain stable until late stages of senescence, whereas the number and size of plastoglobules increase. Unlike catabolic enzymes, whose level increase, the level of most proteins decreases during senescence, and chloroplast proteins are overrepresented among these. However, the rate of their disappearance is variable, mostly uncoordinated and independent of their inherent stability during earlier developmental stages. Unexpectedly, degradation of chlorophyll‐binding proteins lags behind chlorophyll catabolism. Autophagy and vacuole proteins are retained at relatively high levels, highlighting the role of extra‐plastidic degradation processes especially in late stages of senescence. The observation that chlorophyll catabolism precedes all other catabolic events may suggest that this process enables or signals further catabolic processes in chloroplasts. |
format | Online Article Text |
id | pubmed-6508775 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65087752019-06-26 Chlorophyll catabolism precedes changes in chloroplast structure and proteome during leaf senescence Tamary, Eyal Nevo, Reinat Naveh, Leah Levin‐Zaidman, Smadar Kiss, Vladimir Savidor, Alon Levin, Yishai Eyal, Yoram Reich, Ziv Adam, Zach Plant Direct Original Research The earliest visual changes of leaf senescence occur in the chloroplast as chlorophyll is degraded and photosynthesis declines. Yet, a comprehensive understanding of the sequence of catabolic events occurring in chloroplasts during natural leaf senescence is still missing. Here, we combined confocal and electron microscopy together with proteomics and biochemistry to follow structural and molecular changes during Arabidopsis leaf senescence. We observed that initiation of chlorophyll catabolism precedes other breakdown processes. Chloroplast size, stacking of thylakoids, and efficiency of PSII remain stable until late stages of senescence, whereas the number and size of plastoglobules increase. Unlike catabolic enzymes, whose level increase, the level of most proteins decreases during senescence, and chloroplast proteins are overrepresented among these. However, the rate of their disappearance is variable, mostly uncoordinated and independent of their inherent stability during earlier developmental stages. Unexpectedly, degradation of chlorophyll‐binding proteins lags behind chlorophyll catabolism. Autophagy and vacuole proteins are retained at relatively high levels, highlighting the role of extra‐plastidic degradation processes especially in late stages of senescence. The observation that chlorophyll catabolism precedes all other catabolic events may suggest that this process enables or signals further catabolic processes in chloroplasts. John Wiley and Sons Inc. 2019-03-20 /pmc/articles/PMC6508775/ /pubmed/31245770 http://dx.doi.org/10.1002/pld3.127 Text en © 2019 The Authors. Plant Direct published by American Society of Plant Biologists, Society for Experimental Biology and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Tamary, Eyal Nevo, Reinat Naveh, Leah Levin‐Zaidman, Smadar Kiss, Vladimir Savidor, Alon Levin, Yishai Eyal, Yoram Reich, Ziv Adam, Zach Chlorophyll catabolism precedes changes in chloroplast structure and proteome during leaf senescence |
title | Chlorophyll catabolism precedes changes in chloroplast structure and proteome during leaf senescence |
title_full | Chlorophyll catabolism precedes changes in chloroplast structure and proteome during leaf senescence |
title_fullStr | Chlorophyll catabolism precedes changes in chloroplast structure and proteome during leaf senescence |
title_full_unstemmed | Chlorophyll catabolism precedes changes in chloroplast structure and proteome during leaf senescence |
title_short | Chlorophyll catabolism precedes changes in chloroplast structure and proteome during leaf senescence |
title_sort | chlorophyll catabolism precedes changes in chloroplast structure and proteome during leaf senescence |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6508775/ https://www.ncbi.nlm.nih.gov/pubmed/31245770 http://dx.doi.org/10.1002/pld3.127 |
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