Evidence map›Paper›PMID 34064964›Full record

ArticlePlants (Basel, Switzerland)2021

PRAT Proteins Operate in Organellar Protein Import and Export in

Claudia Rossig, John Gray, Oscar Valdes, Armin Springer, Sachin Rustgi, Diter von Wettstein, Christiane Reinbothe, Joachim Rassow, Steffen Reinbothe

Open access · goldAbstract read
In one paragraph

Article in Plants (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 48% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

9 authors at 5 institutions in 3 countries.

Claudia RossigLaboratoire de Génétique Moléculaire des Plantes, Université Grenoble-Alpes, BP53F, 38041 Grenoble, France.ORCID 0000-0002-6756-2337
John GrayDepartment of Biological Sciences, University of Toledo, 2801 West Bancroft Street, Toledo, OH 43606, USA.ORCID 0000-0003-1352-2900
Oscar ValdesLaboratoire de Génétique Moléculaire des Plantes, Université Grenoble-Alpes, BP53F, 38041 Grenoble, France.
Armin SpringerMedical Biology and Electron Microscopy Centre, University Medical Center Rostock, Strempelstraße 14, 18057 Rostock, Germany.
Sachin RustgiDepartment of Plant and Environmental Sciences, Pee Dee Research and Education Center, Clemson University, Florence, SC 29506, USA.ORCID 0000-0002-6881-9501
Diter von WettsteinDepartment of Crop and Soil Sciences, Washington State University, Pullman, WA 99164, USA.
Christiane ReinbotheLaboratoire de Génétique Moléculaire des Plantes, Université Grenoble-Alpes, BP53F, 38041 Grenoble, France.
Joachim RassowDepartment of Cell Biochemistry, Institute for Biochemistry and Pathobiochemistry, Ruhr-University Bochum, Universitätsstraße 150, 44780 Bochum, Germany.
Steffen ReinbotheLaboratoire de Génétique Moléculaire des Plantes, Université Grenoble-Alpes, BP53F, 38041 Grenoble, France.
Université Grenoble Alpes · FRWashington State University · USRuhr University Bochum · DEUniversity of Rostock · DEUniversity of Toledo · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chloroplasts need to import preproteins and amino acids from the cytosol during their light-induced differentiation. Similarly, chloroplasts have to export organic matter including proteins and amino acids during leaf senescence. Members of the PRAT (preprotein and amino acid transporter) family are candidate transporters for both processes. Here, we defined the role of two small PRAT gene families, At4g26670 and At5g55510 (HP20 subfamily) versus At3g49560 and At5g24650 (HP30 subfamily) during greening of etiolated plants and during leaf senescence. Using a combination of reverse genetics, protein biochemistry and physiological tools, evidence was obtained for a role of chloroplast HP20, HP30 and HP30-2 in protein, but not amino acid, import into chloroplasts. HP20, HP30 and HP30-2 form larger complexes involved in the uptake of transit sequence-less cytosolic precursors. In addition, we identified a fraction of HP30-2 in mitochondria where it served a similar function as found for chloroplasts and operated in the uptake of transit sequence-less cytosolic precursor proteins. By contrast, HP22 was found to act in the export of proteins from chloroplasts during leaf senescence, and thus its role is entirely different from that of its orthologue, HP20. HP22 is part of a unique protein complex in the envelope of senescing chloroplasts that comprises at least 11 proteins and contains with HP65b (At5g55220) a protein that is related to the bacterial trigger factor chaperone. An ortholog of HP65b exists in the cyanobacterium

Indexed as

chloroplast and mitochondrial membrane transportplant greening and senescencepreprotein and amino acid transporter (PRAT) familyprotein translocation

Identifiers

PMID34064964
PMCPMC8151980
OpenAlexW3160086096

What OpenQuestion holds

Textmetadata
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.