Evidence map›Paper›PMID 23906065›Full record

ArticleDevelopmental cell2013

Daughter cell identity emerges from the interplay of Cdc42, septins, and exocytosis.

Satoshi Okada, Marcin Leda, Julia Hanna, Natasha S Savage, Erfei Bi, Andrew B Goryachev

Open access · hybridAbstract read
In one paragraph

Article in Developmental cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 93 papers.

0numbers the graph read from it
0cells of the map it votes in
93citing papers in PubMed
5.7field-weighted citation impact, top 3% 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

93 citing papers in PubMed, 158 citations in OpenAlex.

  1. Polarization as a Process: The Potential of Process Ontology for Understanding Cellular Symmetry Breaking.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Roles for the canonical polarity machinery in thebioRxiv : the preprint server for biology · 2025
    Article
  8. Article
  9. Article
  10. Septin Organization and Dynamics for Budding Yeast Cytokinesis.Journal of fungi (Basel, Switzerland) · 2024
    Review
  11. Article
  12. Article
  13. Patterning of the cell cortex by Rho GTPases.Nature reviews. Molecular cell biology · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

33 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Satoshi OkadaDepartment of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Marcin Leda
Julia Hanna
Natasha S Savage
Erfei Bi
Andrew B Goryachev
University of Edinburgh · GBUniversity of Pennsylvania · US

Funding

UNIVERSITY OF PENNSYLVANIA CAN CTR SUPPORT GRANTP30CA016520 · NCI · UNIVERSITY OF PENNSYLVANIA · PI SHELLEY L BERGER · 1985 to 2026
$222.3M
SIGNALING MECHANISMS IN CELL POLARITY IN YEASTR01GM059216 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI BI, ERFEI · 1999 to 2012
$3.8M
Mechanisms of Cytokinesis in YeastR01GM087365 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI BI, ERFEI · 2010 to 2013
$1.2M
Biotechnology and Biological Sciences Research Council BB/G001855/1Biotechnology and Biological Sciences Research Council G001855NCI NIH HHS P30 CA016520NIGMS NIH HHS GM59216NIGMS NIH HHS GM87365NIGMS NIH HHS R01 GM059216NIGMS NIH HHS R01 GM087365Wellcome Trust
6 · The paper itself

Abstract

Asymmetric cell division plays a crucial role in cell differentiation, unequal replicative senescence, and stem cell maintenance. In budding yeast, the identities of mother and daughter cells begin to diverge at bud emergence when distinct plasma-membrane domains are formed and separated by a septin ring. However, the mechanisms underlying this transformation remain unknown. Here, we show that septins recruited to the site of polarization by Cdc42-GTP inhibit Cdc42 activity in a negative feedback loop, and this inhibition depends on Cdc42 GTPase-activating proteins. Combining live-cell imaging and computational modeling, we demonstrate that the septin ring is sculpted by polarized exocytosis, which creates a hole in the accumulating septin density and relieves the inhibition of Cdc42. The nascent ring generates a sharp boundary that confines the Cdc42 activity and exocytosis strictly to its enclosure and thus clearly delineates the daughter cell identity. Our findings define a fundamental mechanism underlying eukaryotic cell fate differentiation.

Indexed as

cdc42 GTP-Binding Protein, Saccharomyces cerevisiaeCell Cycle ProteinsCell DivisionCytoskeletal ProteinsCytoskeletonExocytosisFeedback, PhysiologicalSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSeptinscdc42 GTP-Binding Protein, Saccharomyces cerevisiaeCell Cycle ProteinsCytoskeletal ProteinsSaccharomyces cerevisiae ProteinsSeptins

Identifiers

PMID23906065
PMCPMC3730058
OpenAlexW2020017362

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.