Evidence map›Paper›PMID 27492982›Full record

ArticleJournal of experimental botany2016

Developmental programmed cell death during asymmetric microsporogenesis in holocentric species of Rhynchospora (Cyperaceae).

Danilo M Rocha, André Marques, Celia G T J Andrade, Romain Guyot, Srinivasa R Chaluvadi, Andrea Pedrosa-Harand, Andreas Houben, Jeffrey L Bennetzen, André L L Vanzela

Open access · hybridAbstract read
In one paragraph

Article in Journal of experimental botany, 2016. 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
2.6field-weighted citation impact, top 8% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Holocentric Karyotype Evolution inFrontiers in plant science · 2020
    Article
  10. Article
  11. Article
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 4 countries.

Danilo M RochaLaboratory of Cytogenetics and Plant Diversity, Department of General Biology, Center of Biological Sciences, State University of Londrina, Londrina 86057-970, Paraná, Brazil.
André MarquesLaboratory of Plant Cytogenetics and Evolution, Department of Botany, Federal University of Pernambuco, Recife, Brazil.
Celia G T J AndradeLaboratory of Electron Microscopy and Microanalysis, Pro-PPG, State University of Londrina, 86051990, Londrina, Brazil.
Romain GuyotInstitut de Recherche pour le Développement (IRD), UMR IPME, BP 64501, 34394, Montpellier Cedex, France.
Srinivasa R ChaluvadiDepartment of Genetics, University of Georgia, Athens, GA 30602, USA.
Andrea Pedrosa-HarandLaboratory of Plant Cytogenetics and Evolution, Department of Botany, Federal University of Pernambuco, Recife, Brazil.
Andreas HoubenLeibniz Institute of Plant Genetics and Crop Plant Research (IPK) Gatersleben, D-06466 Stadt Seeland, Germany.
Jeffrey L BennetzenDepartment of Genetics, University of Georgia, Athens, GA 30602, USA.
André L L VanzelaLaboratory of Cytogenetics and Plant Diversity, Department of General Biology, Center of Biological Sciences, State University of Londrina, Londrina 86057-970, Paraná, Brazil andrevanzela@uel.br.
Universidade Estadual de Londrina · BRUniversidade Federal de Pernambuco · BRUniversity of Georgia · USAgropolis International · FRLeibniz Institute of Plant Genetics and Crop Plant Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Members of the Cyperaceae family exhibit an asymmetric microsporogenesis that results in the degeneration of three out of four meiotic products. Efforts have been made previously to describe the resulting structure, named the pseudomonad, but mechanisms concerning the establishment of cell domains, nuclear development, and programmed cell death are largely unknown. Using the Rhynchospora genus as a model, evidence for cell asymmetry, cytoplasmic isolation, and programmed cell death was obtained by a combination of electron microscopic, cytochemical, immunocytochemical, in situ hybridization, and flow cytometric methods. Degenerative cells were identified at the abaxial region, with the cytoskeleton marking their delimitation from the functional domain after meiosis. After attempting to initiate cell division with an unreplicated genome and abnormal spindle assembly, these cells exhibited a gradual process of cytoplasmic contraction associated with hypermethylation of cytosines and differential loss of DNA. These results indicate that the asymmetric tetrad establishes a functional cell, where one nucleus is preferentially selected to survive. Degenerative haploid cells are then eliminated in a multistep process associated with mitotic disorder, non-random elimination of repetitive DNA, vacuolar cell death, and DNA fragmentation.

Indexed as

Cell DeathCell DivisionCyperaceaeCytoplasmCytoskeletonGametogenesis, PlantIn Situ HybridizationMeiosisMicroscopy, ElectronAsymmetric cell plateelectron microscopyholocentromeresmeiotic drivemitotic disorderpollen developmentvacuolar cell death.

Identifiers

PMID27492982
PMCPMC5049389
OpenAlexW2503263996

What OpenQuestion holds

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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.