Evidence map›Paper›PMID 23225155›Full record

ArticlePlant molecular biology2013

Analysis of the chloroplast proteome in arc mutants and identification of novel protein components associated with FtsZ2.

Daniela Gargano, Jodi Maple-Grødem, Veronika Reisinger, Lutz Andreas Eichacker, Simon Geir Møller

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Article in Plant molecular biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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  6. Review
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

5 authors.

Daniela GarganoCentre for Organelle Research, University of Stavanger, Stavanger, Norway.
Jodi Maple-Grødem
Veronika Reisinger
Lutz Andreas Eichacker
Simon Geir Møller

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chloroplasts are descendants of cyanobacteria and divide by binary fission. The number of chloroplasts is regulated in a cell type-specific manner to ensure that specialized cell types can perform their functions optimally. Several protein components of the chloroplast division apparatus have been identified in the past several years, but how this process is regulated in response to developmental status, environmental signals and stress is still unknown. To begin to address this we undertook a proteomic analysis of three accumulation and replication of chloroplasts mutants that show a spectrum of plastid division perturbations. We show that defects in the chloroplast division process results in changes in the abundance of proteins when compared to wild type, but that the profile of the native stromal and membrane complexes remains unchanged. Furthermore, by combining BN-PAGE with protein interaction assays we show that AtFtsZ2-1 and AtFtsZ2-2 assemble together with rpl12A and EF-Tu into a novel chloroplast membrane complex.

Indexed as

ProteomeAmino Acid SequenceArabidopsisArabidopsis ProteinsChloroplast ProteinsChloroplastsChromatography, High Pressure LiquidGene Expression Regulation, PlantMutationNicotianaPeptide Elongation Factor TuPlant LeavesPlants, Genetically ModifiedProteomicsSaccharomyces cerevisiaeSeedlingsArabidopsis ProteinsAtFtsZ2 protein, ArabidopsisChloroplast ProteinsPeptide Elongation Factor TuProteome

Identifiers

What OpenQuestion holds

Textmetadata
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.