Evidence map›Paper›PMID 28878206›Full record

ArticleNature communications2017

Towards designer organelles by subverting the peroxisomal import pathway.

Laura L Cross, Rupesh Paudyal, Yasuko Kamisugi, Alan Berry, Andrew C Cuming, Alison Baker, Stuart L Warriner

Abstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. The Promise of Synthetic Biology for Redesigning Plant Architecture.International journal of molecular sciences · 2026
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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

7 authors.

Laura L CrossAstbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS2 9JT, UK.ORCID http://orcid.org/0000-0002-8167-1329
Rupesh PaudyalSchool of Molecular and Cellular Biology, University of Leeds, Leeds, LS2 9JT, UK.ORCID http://orcid.org/0000-0002-1849-7313
Yasuko KamisugiThe Centre for Plant Sciences, University of Leeds, Leeds, LS2 9JT, UK.ORCID http://orcid.org/0000-0002-5265-3658
Alan BerryAstbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS2 9JT, UK.ORCID http://orcid.org/0000-0003-3502-0426
Andrew C CumingThe Centre for Plant Sciences, University of Leeds, Leeds, LS2 9JT, UK.ORCID http://orcid.org/0000-0003-2562-2052
Alison BakerAstbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS2 9JT, UK. a.baker@leeds.ac.uk.ORCID http://orcid.org/0000-0003-2181-4057
Stuart L WarrinerAstbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS2 9JT, UK. s.l.warriner@leeds.ac.uk.ORCID http://orcid.org/0000-0002-7589-6011

Funding

Wellcome Trust
6 · The paper itself

Abstract

The development of 'designer' organelles could be a key strategy to enable foreign pathways to be efficiently controlled within eukaryotic biotechnology. A fundamental component of any such system will be the implementation of a bespoke protein import pathway that can selectively deliver constituent proteins to the new compartment in the presence of existing endogenous trafficking systems. Here we show that the protein-protein interactions that control the peroxisomal protein import pathway can be manipulated to create a pair of interacting partners that still support protein import in moss cells, but are orthogonal to the naturally occurring pathways. In addition to providing a valuable experimental tool to give new insights into peroxisomal protein import, the variant receptor-signal sequence pair forms the basis of a system in which normal peroxisomal function is downregulated and replaced with an alternative pathway, an essential first step in the creation of a designer organelle.Designer organelles could allow the isolation of synthetic biological pathways from endogenous components of the host cell. Here the authors engineer a peroxisomal protein import pathway orthogonal to the naturally occurring system.

Indexed as

ArabidopsisArabidopsis ProteinsPeptidesPeroxisomesProtein BindingProtein TransportArabidopsis ProteinsPeptides

Identifiers

PMID28878206
PMCPMC5587766

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.