Evidence map›Paper›PMID 31245770›Full record

ArticlePlant direct2019

Chlorophyll catabolism precedes changes in chloroplast structure and proteome during leaf senescence.

Eyal Tamary, Reinat Nevo, Leah Naveh, Smadar Levin-Zaidman, Vladimir Kiss, Alon Savidor, Yishai Levin, Yoram Eyal, Ziv Reich, Zach Adam

Open access · goldAbstract read
In one paragraph

Article in Plant direct, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
4.6field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 94 citations in OpenAlex.

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  13. Expression and function identification of senescence-associated genes under continuous drought treatment in grapevine (Physiology and molecular biology of plants : an international journal of functional plant biology · 2024
    Article
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  15. Overexpression ofFrontiers in plant science · 2024
    Article
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  18. Review
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  20. Ecophysiology of Endangered Plant SpeciesPlants (Basel, Switzerland) · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Eyal TamaryThe Robert H. Smith Institute of Plant Sciences and Genetics in Agriculture The Hebrew University Rehovot Israel.
Reinat NevoDepartment of Biomolecular Sciences Weizmann Institute of Science Rehovot Israel.
Leah NavehThe Robert H. Smith Institute of Plant Sciences and Genetics in Agriculture The Hebrew University Rehovot Israel.
Smadar Levin-ZaidmanDepartment of Chemical Research Support Weizmann Institute of Science Rehovot Israel.
Vladimir KissDepartment of Biomolecular Sciences Weizmann Institute of Science Rehovot Israel.
Alon Savidorde Botton Institute for Protein Profiling The Nancy and Stephen Grand Israel National Center for Personalized Medicine Weizmann Institute of Science Rehovot Israel.
Yishai Levinde Botton Institute for Protein Profiling The Nancy and Stephen Grand Israel National Center for Personalized Medicine Weizmann Institute of Science Rehovot Israel.
Yoram EyalInstitute of Plant Sciences The Volcani Center ARO Rishon LeZion Israel.
Ziv ReichDepartment of Biomolecular Sciences Weizmann Institute of Science Rehovot Israel.
Zach AdamThe Robert H. Smith Institute of Plant Sciences and Genetics in Agriculture The Hebrew University Rehovot Israel.
Weizmann Institute of Science · ILHebrew University of Jerusalem · ILAgricultural Research Organization · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Arabidopsischlorophyllchloroplastphotosynthesisplastoglobulesenescencethylakoid

Identifiers

PMID31245770
PMCPMC6508775
OpenAlexW2923878455

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.