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|a 10.1093/jxb/erx234
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|a eng
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1 |
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|a Otegui, Marisa S
|e verfasserin
|4 aut
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|a Vacuolar degradation of chloroplast components
|b autophagy and beyond
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| 264 |
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1 |
|c 2018
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|a Text
|b txt
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|a ƒaComputermedien
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|a Date Completed 29.07.2019
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|a Date Revised 29.07.2019
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|a published: Print
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|a Citation Status MEDLINE
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| 520 |
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|a © The Author(s) 2017. Published by Oxford University Press on behalf of the Society for Experimental Biology. All rights reserved. For permissions, please email: journals.permissionsoup.com.
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|a Chloroplast degradation during natural or stress-induced senescence requires the participation of both plastidic and extraplastidic degradative pathways. As part of the extraplastidic pathways, chloroplasts export stroma, envelope, and thylakoid proteins in membrane-bound organelles that are ultimately degraded in vacuoles. Some of these pathways, such as the formation of senescence-associated vacuoles (SAVs) and CV-containing vesicles (CCVs), do not depend on autophagy, whereas delivery of Rubisco-containing bodies (RCBs), ATI1-PS (ATG8-interacting Protein 1) bodies, and small starch-like granule (SSLG) bodies is autophagy dependent. In addition, autophagy of entire chloroplasts delivers damaged chloroplasts into the vacuolar lumen for degradation. This review summarizes the autophagy-dependent and independent trafficking mechanisms by which plant cells degrade chloroplast components in vacuoles
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|a Journal Article
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|a Research Support, U.S. Gov't, Non-P.H.S.
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|a Review
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|a Autophagy
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| 650 |
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|a CV vesicles
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| 650 |
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4 |
|a chlorophagy
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| 650 |
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4 |
|a chloroplast
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| 650 |
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4 |
|a senescence
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| 650 |
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4 |
|a senescence-associated vacuoles
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4 |
|a starch
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|i Enthalten in
|t Journal of experimental botany
|d 1985
|g 69(2018), 4 vom: 12. Feb., Seite 741-750
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|g year:2018
|g number:4
|g day:12
|g month:02
|g pages:741-750
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