Evidence map›Paper›PMID 27821733›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2016

A Diaphanous-related formin links Ras signaling directly to actin assembly in macropinocytosis and phagocytosis.

Alexander Junemann, Vedrana Filić, Moritz Winterhoff, Benjamin Nordholz, Christof Litschko, Helena Schwellenbach, Till Stephan, Igor Weber, Jan Faix

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

41 citing papers in PubMed, 75 citations in OpenAlex.

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  13. Convergence of Ras- and Rac-regulated formin pathways is pivotal for phagosome formation and particle uptake inProceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  14. Macropinocytosis inFrontiers in plant science · 2023
    Article
  15. Article
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  18. Article
  19. Gradients of PI(4,5)PFrontiers in cell and developmental biology · 2022
    Article
  20. The Amoebal Model for Macropinocytosis.Sub-cellular biochemistry · 2022
    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 2 institutions in 2 countries.

Alexander JunemannInstitute for Biophysical Chemistry, Hannover Medical School, 30625 Hannover, Germany.
Vedrana FilićDivision of Molecular Biology, Ruđer Bošković Institute, 10000 Zagreb, Croatia.
Moritz WinterhoffInstitute for Biophysical Chemistry, Hannover Medical School, 30625 Hannover, Germany.
Benjamin NordholzInstitute for Biophysical Chemistry, Hannover Medical School, 30625 Hannover, Germany.
Christof LitschkoInstitute for Biophysical Chemistry, Hannover Medical School, 30625 Hannover, Germany.
Helena SchwellenbachInstitute for Biophysical Chemistry, Hannover Medical School, 30625 Hannover, Germany.
Till StephanInstitute for Biophysical Chemistry, Hannover Medical School, 30625 Hannover, Germany.
Igor WeberDivision of Molecular Biology, Ruđer Bošković Institute, 10000 Zagreb, Croatia.
Jan FaixInstitute for Biophysical Chemistry, Hannover Medical School, 30625 Hannover, Germany; faix.jan@mh-hannover.de.
Medizinische Hochschule Hannover · DERudjer Boskovic Institute · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phagocytosis and macropinocytosis are Ras-regulated and actin-driven processes that depend on the dynamic rearrangements of the plasma membrane that protrudes and internalizes extracellular material by cup-shaped structures. However, the regulatory mechanisms underlying actin assembly in large-scale endocytosis remain elusive. Here, we show that the Diaphanous-related formin G (ForG) from the professional phagocyte Dictyostelium discoideum localizes to endocytic cups. Biochemical analyses revealed that ForG is a rather weak nucleator but efficiently elongates actin filaments in the presence of profilin. Notably, genetic inactivation of ForG is associated with a strongly impaired endocytosis and a markedly diminished F-actin content at the base of the cups. By contrast, ablation of the Arp2/3 (actin-related protein-2/3) complex activator SCAR (suppressor of cAMP receptor) diminishes F-actin mainly at the cup rim, being consistent with its known localization. These data therefore suggest that ForG acts as an actin polymerase of Arp2/3-nucleated filaments to allow for efficient membrane expansion and engulfment of extracellular material. Finally, we show that ForG is directly regulated in large-scale endocytosis by RasB and RasG, which are highly related to the human proto-oncogene KRas.

Indexed as

Actin-Related Protein 2-3 ComplexActinsDictyosteliumMicrofilament ProteinsMutationPhagocytosisPinocytosisProto-Oncogene MasProtozoan Proteinsras ProteinsSignal TransductionActin-Related Protein 2-3 ComplexActinsMAS1 protein, humanMicrofilament ProteinsProto-Oncogene MasProtozoan Proteinsras ProteinsArp2/3 complexforminmacropinocytosisphagocytosisRas

Identifiers

PMID27821733
PMCPMC5127317
OpenAlexW2555843119

What OpenQuestion holds

Textmetadata
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.