Evidence map›Paper›PMID 37324680›Full record

ArticleFrontiers in plant science2023

The EXO70 inhibitor Endosidin2 alters plasma membrane protein composition in Arabidopsis roots.

Xiaohui Li, Peipei Zhu, Yen-Ju Chen, Lei Huang, Diwen Wang, David T Newton, Chuan-Chih Hsu, Guang Lin, W Andy Tao, Christopher J Staiger and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in plant science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Xiaohui LiDepartment of Botany and Plant Pathology, Purdue University, West Lafayette, IN, United States.
Peipei ZhuDepartment of Biochemistry, Purdue University, West Lafayette, IN, United States.
Yen-Ju ChenDepartment of Botany and Plant Pathology, Purdue University, West Lafayette, IN, United States.
Lei HuangDepartment of Botany and Plant Pathology, Purdue University, West Lafayette, IN, United States.
Diwen WangDepartment of Botany and Plant Pathology, Purdue University, West Lafayette, IN, United States.
David T NewtonDepartment of Statistics, Purdue University, West Lafayette, IN, United States.
Chuan-Chih HsuDepartment of Biochemistry, Purdue University, West Lafayette, IN, United States.
Guang LinDepartment of Mathematics, Purdue University, West Lafayette, IN, United States.
W Andy TaoDepartment of Biochemistry, Purdue University, West Lafayette, IN, United States.
Christopher J StaigerDepartment of Botany and Plant Pathology, Purdue University, West Lafayette, IN, United States.
Chunhua ZhangDepartment of Botany and Plant Pathology, Purdue University, West Lafayette, IN, United States.
Purdue University West Lafayette · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To sustain normal growth and allow rapid responses to environmental cues, plants alter the plasma membrane protein composition under different conditions presumably by regulation of delivery, stability, and internalization. Exocytosis is a conserved cellular process that delivers proteins and lipids to the plasma membrane or extracellular space in eukaryotes. The octameric exocyst complex contributes to exocytosis by tethering secretory vesicles to the correct site for membrane fusion; however, whether the exocyst complex acts universally for all secretory vesicle cargo or just for specialized subsets used during polarized growth and trafficking is currently unknown. In addition to its role in exocytosis, the exocyst complex is also known to participate in membrane recycling and autophagy. Using a previously identified small molecule inhibitor of the plant exocyst complex subunit EXO70A1, Endosidin2 (ES2), combined with a plasma membrane enrichment method and quantitative proteomic analysis, we examined the composition of plasma membrane proteins in the root of Arabidopsis seedlings, after inhibition of the ES2-targetted exocyst complex, and verified our findings by live imaging of GFP-tagged plasma membrane proteins in root epidermal cells. The abundance of 145 plasma membrane proteins was significantly reduced following short-term ES2 treatments and these likely represent candidate cargo proteins of exocyst-mediated trafficking. Gene Ontology analysis showed that these proteins play diverse functions in cell growth, cell wall biosynthesis, hormone signaling, stress response, membrane transport, and nutrient uptake. Additionally, we quantified the effect of ES2 on the spatial distribution of EXO70A1 with live-cell imaging. Our results indicate that the plant exocyst complex mediates constitutive dynamic transport of subsets of plasma membrane proteins during normal root growth.

Indexed as

exocystexocytosisplasma membrane protein enrichmentproteomicssmall molecule inhibitors

Identifiers

PMID37324680
PMCPMC10264680
OpenAlexW4378902141

What OpenQuestion holds

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Registered trials

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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.