Evidence map›Paper›PMID 29444117›Full record

ArticlePloS one2018

An ancestral TMEM16 homolog from Dictyostelium discoideum forms a scramblase.

Thomas Pelz, Daniela R Drose, David Fleck, Bastian Henkel, Tobias Ackels, Marc Spehr, Eva M Neuhaus

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Polymodal Control of TMEM16x Channels and Scramblases.International journal of molecular sciences · 2022
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. The Journal of biological chemistry · 2019
    Article
  10. Anoctamin 5/TMEM16E facilitates muscle precursor cell fusion.The Journal of general physiology · 2018
    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

7 authors.

Thomas PelzPharmacology and Toxicology, Jena University Hospital, Friedrich Schiller University Jena, Jena, Germany.
Daniela R DroseDepartment of Chemosensation, Institute for Biology II, RWTH-Aachen University, Aachen, Germany.
David FleckDepartment of Chemosensation, Institute for Biology II, RWTH-Aachen University, Aachen, Germany.
Bastian HenkelPharmacology and Toxicology, Jena University Hospital, Friedrich Schiller University Jena, Jena, Germany.
Tobias AckelsDepartment of Chemosensation, Institute for Biology II, RWTH-Aachen University, Aachen, Germany.
Marc SpehrDepartment of Chemosensation, Institute for Biology II, RWTH-Aachen University, Aachen, Germany.
Eva M NeuhausPharmacology and Toxicology, Jena University Hospital, Friedrich Schiller University Jena, Jena, Germany.ORCID 0000-0003-3363-1231

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TMEM16 proteins are a recently identified protein family comprising Ca2+-activated Cl- channels that generate outwardly rectifying ionic currents in response to intracellular Ca2+ elevations. Some TMEM16 family members, such as TMEM16F/ANO6 are also essential for Ca2+-dependent phospholipid scrambling. TMEM16-like genes are present in the genomes of most eukaryotic species, the function(s) of TMEM16 family members from evolutionary ancient eukaryotes is not completely clear. Here, we provide insight into the evolution of these TMEM16 proteins by similarity searches for ancestral sequences. All eukaryotic genomes contain TMEM16 homologs, but only vertebrates have the full repertoire of ten distinct subtypes. TMEM16 homologs studied so far belong to the opisthokont branch of the phylogenetic tree, which includes the animal and fungal kingdoms. An organism outside this group is Dictyostelium discoideum, a representative of the amoebozoa group that diverged from the metazoa before fungi. We here functionally investigated the TMEM16 family member from Dictyostelium discoideum. When recombinantly expressed in HEK293 cells, DdTMEM16 induces phospholipid scrambling. However, in several electrophysiological experiments we did not find evidence for a Ca2+-activated Cl- channel function of DdTMEM16.

Indexed as

AnimalsAnoctaminsBiological EvolutionChloride ChannelsDictyosteliumEukaryotaEvolution, MolecularHEK293 CellsHumansIon TransportPhospholipidsPhospholipid Transfer ProteinsPhylogenyRecombinant ProteinsAnoctaminsChloride ChannelsPhospholipidsPhospholipid Transfer ProteinsRecombinant Proteins

Identifiers

PMID29444117
PMCPMC5812556

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.