Evidence map›Paper›PMID 38829834›Full record

ArticlePlant physiology2024

Principles of amyloplast replication in the ovule integuments of Arabidopsis thaliana.

Makoto T Fujiwara, Yasushi Yoshioka, Yusuke Kazama, Tomonari Hirano, Yasuo Niwa, Takashi Moriyama, Naoki Sato, Tomoko Abe, Shigeo Yoshida, Ryuuichi D Itoh

Abstract read
In one paragraph

Article in Plant physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

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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.

Makoto T FujiwaraNishina Center and Plant Functions Laboratory (Disbanded in March 2004), RIKEN, Wako, Saitama 351-0198, Japan.ORCID 0000-0002-4668-276X
Yasushi YoshiokaGraduate School of Science, Nagoya University, Furo-cho, Nagoya 464-8602, Japan.ORCID 0009-0007-6584-5871
Yusuke KazamaNishina Center and Plant Functions Laboratory (Disbanded in March 2004), RIKEN, Wako, Saitama 351-0198, Japan.ORCID 0000-0001-5876-7755
Tomonari HiranoNishina Center and Plant Functions Laboratory (Disbanded in March 2004), RIKEN, Wako, Saitama 351-0198, Japan.ORCID 0000-0003-0071-8058
Yasuo NiwaLaboratory of Plant Cell Technology, University of Shizuoka, Yada, Shizuoka 422-8526, Japan.
Takashi MoriyamaCollege of Arts and Sciences, University of Tokyo, Komaba, Tokyo 153-8902, Japan.ORCID 0009-0009-9149-749X
Naoki SatoCollege of Arts and Sciences, University of Tokyo, Komaba, Tokyo 153-8902, Japan.ORCID 0000-0001-6230-0410
Tomoko AbeNishina Center and Plant Functions Laboratory (Disbanded in March 2004), RIKEN, Wako, Saitama 351-0198, Japan.ORCID 0000-0001-5928-4683
Shigeo YoshidaNishina Center and Plant Functions Laboratory (Disbanded in March 2004), RIKEN, Wako, Saitama 351-0198, Japan.
Ryuuichi D ItohDepartment of Chemistry, Biology and Marine Science, Faculty of Science, University of the Ryukyus, Senbaru 1, Nishihara, Okinawa 903-0213, Japan.ORCID 0000-0002-5786-2176

Funding

Agricultural Chemical Research FoundationJGC-S Scholarship FoundationMinistry of Education, Culture, Sports, Science and Technology of Japan 14760068Special Postdoctoral Research Program of RIKEN
6 · The paper itself

Abstract

Plastids in vascular plants have various differentiated forms, among which amyloplasts are crucial for starch storage and plant productivity. Despite the vast knowledge of the binary-fission mode of chloroplast division, our understanding of the replication of non-photosynthetic plastids, including amyloplasts, remains limited. Recent studies have suggested the involvement of stromules (stroma-filled tubules) in plastid replication when the division apparatus is faulty. However, details of the underlying mechanism(s) and their relevance to normal processes have yet to be elucidated. Here, we developed a live analysis system for studying amyloplast replication using Arabidopsis (Arabidopsis thaliana) ovule integuments. We showed the full sequence of amyloplast development and demonstrated that wild-type amyloplasts adopt three modes of replication, binary fission, multiple fission, and stromule-mediated fission, via multi-way placement of the FtsZ ring. The minE mutant, with severely inhibited chloroplast division, showed marked heterogeneity in amyloplast size, caused by size-dependent but wild-type modes of plastid fission. The dynamic properties of stromules distinguish the wild-type and minE phenotypes. In minE cells, extended stromules from giant amyloplasts acquired stability, allowing FtsZ ring assembly and constriction, as well as the growth of starch grains therein. Despite hyper-stromule formation, amyloplasts did not proliferate in the ftsZ null mutant. These data clarify the differences between amyloplast and chloroplast replication and demonstrate that the structural plasticity of amyloplasts underlies the multiplicity of their replication processes. Furthermore, this study shows that stromules can generate daughter plastids via the assembly of the FtsZ ring.

Indexed as

ArabidopsisArabidopsis ProteinsOvulePlastidsChloroplastsMutationPhenotypeArabidopsis ProteinsFTSZ protein, Arabidopsis

Identifiers

PMID38829834
PMCPMC11376375

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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.