Evidence map›Paper›PMID 24348496›Full record

ArticleFrontiers in plant science2013

Reprogramming cells to study vacuolar development.

Mistianne Feeney, Lorenzo Frigerio, Susanne E Kohalmi, Yuhai Cui, Rima Menassa

Open access · goldAbstract read
In one paragraph

Article in Frontiers in plant science, 2013. 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
0.5field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. AtCAP2 is crucial for lytic vacuole biogenesis during germination by positively regulating vacuolar protein trafficking.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  4. The increasing value of plant-made proteins.Current opinion in biotechnology · 2015
    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 at 4 institutions in 2 countries.

Mistianne FeeneyDepartment of Biology, University of Western Ontario London, ON, Canada ; Southern Crop Protection and Food Research Centre, Agriculture and Agri-Food Canada London, ON, Canada ; School of Life Sciences, University of Warwick Coventry, UK.
Lorenzo FrigerioSchool of Life Sciences, University of Warwick Coventry, UK.
Susanne E KohalmiDepartment of Biology, University of Western Ontario London, ON, Canada.
Yuhai CuiDepartment of Biology, University of Western Ontario London, ON, Canada ; Southern Crop Protection and Food Research Centre, Agriculture and Agri-Food Canada London, ON, Canada.
Rima MenassaDepartment of Biology, University of Western Ontario London, ON, Canada ; Southern Crop Protection and Food Research Centre, Agriculture and Agri-Food Canada London, ON, Canada.
University of Warwick · GBAgriculture and Agri-Food Canada · CALondon Research and Development CentreWestern University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During vegetative and embryonic developmental transitions, plant cells are massively reorganized to support the activities that will take place during the subsequent developmental phase. Studying cellular and subcellular changes that occur during these short transitional periods can sometimes present challenges, especially when dealing with Arabidopsis thaliana embryo and seed tissues. As a complementary approach, cellular reprogramming can be used as a tool to study these cellular changes in another, more easily accessible, tissue type. To reprogram cells, genetic manipulation of particular regulatory factors that play critical roles in establishing or repressing the seed developmental program can be used to bring about a change of cell fate. During different developmental phases, vacuoles assume different functions and morphologies to respond to the changing needs of the cell. Lytic vacuoles (LVs) and protein storage vacuoles (PSVs) are the two main vacuole types found in flowering plants such as Arabidopsis. Although both are morphologically distinct and carry out unique functions, they also share some similar activities. As the co-existence of the two vacuole types is short-lived in plant cells, how they replace each other has been a long-standing curiosity. To study the LV to PSV transition, LEAFY COTYLEDON2, a key transcriptional regulator of seed development, was overexpressed in vegetative cells to activate the seed developmental program. At the cellular level, Arabidopsis leaf LVs were observed to convert to PSV-like organelles. This presents the opportunity for further research to elucidate the mechanism of LV to PSV transitions. Overall, this example demonstrates the potential usefulness of cellular reprogramming as a method to study cellular processes that occur during developmental transitions.

Indexed as

Arabidopsis thalianacellular reprogrammingdevelopmental transitionLEAFY COTYLEDON2lytic vacuoleprotein storage vacuolevacuole biogenesis

Identifiers

PMID24348496
PMCPMC3848493
OpenAlexW2093947711

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.