Evidence map›Paper›PMID 21041363›Full record

ArticleDevelopment (Cambridge, England)2010

The C. elegans homolog of Drosophila Lethal giant larvae functions redundantly with PAR-2 to maintain polarity in the early embryo.

Alexander Beatty, Diane Morton, Kenneth Kemphues

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

58 citing papers in PubMed, 95 citations in OpenAlex.

  1. Article
  2. Article
  3. LGL-1 and the RhoGAP protein PAC-1 redundantly polarize thebioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
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  11. Origin and development of primary animal epithelia.BioEssays : news and reviews in molecular, cellular and developmental biology · 2024
    Review
  12. Temporally distinct roles of Aurora A in polarization of thebioRxiv : the preprint server for biology · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Single-molecule FISH inmicroPublication biology · 2022
    Article
  18. Article
  19. Article
  20. Polarity scaffolds signaling in epithelial cell permeability.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2021
    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

3 authors at 1 institution in 1 country.

Alexander BeattyDepartment of Molecular Biology and Genetics, Cornell University, 433 Biotechnology Building, Ithaca, NY 14850, USA.
Diane Morton
Kenneth Kemphues
Cornell University · US

Funding

Asymmetric Cell Division in C. Elegans EmbryosR01GM079112 · NIGMS · CORNELL UNIVERSITY · PI KEMPHUES, KENNETH J. · 2006 to 2014
$3.1M
GENETIC ANALYSIS OF EARLY EMBRYOGENESIS IN C ELEGANSR01HD027689 · NICHD · CORNELL UNIVERSITY ITHACA · PI KEMPHUES, KENNETH J. · 1991 to 2005
$2.4M
NICHD NIH HHS HD27689NICHD NIH HHS R01 HD027689NIGMS NIH HHS GM079112NIGMS NIH HHS R01 GM079112
6 · The paper itself

Abstract

Polarity is essential for generating cell diversity. The one-cell C. elegans embryo serves as a model for studying the establishment and maintenance of polarity. In the early embryo, a myosin II-dependent contraction of the cortical meshwork asymmetrically distributes the highly conserved PDZ proteins PAR-3 and PAR-6, as well as an atypical protein kinase C (PKC-3), to the anterior. The RING-finger protein PAR-2 becomes enriched on the posterior cortex and prevents these three proteins from returning to the posterior. In addition to the PAR proteins, other proteins are required for polarity in many metazoans. One example is the conserved Drosophila tumor-suppressor protein Lethal giant larvae (Lgl). In Drosophila and mammals, Lgl contributes to the maintenance of cell polarity and plays a role in asymmetric cell division. We have found that the C. elegans homolog of Lgl, LGL-1, has a role in polarity but is not essential. It localizes asymmetrically to the posterior of the early embryo in a PKC-3-dependent manner, and functions redundantly with PAR-2 to maintain polarity. Furthermore, overexpression of LGL-1 is sufficient to rescue loss of PAR-2 function. LGL-1 negatively regulates the accumulation of myosin (NMY-2) on the posterior cortex, representing a possible mechanism by which LGL-1 might contribute to polarity maintenance.

Indexed as

AllelesAnimalsBody PatterningCaenorhabditis elegansCaenorhabditis elegans ProteinsDrosophilaDrosophila ProteinsEmbryo, NonmammalianEpithelial CellsMutationMyosin Heavy ChainsProtein Kinase CProtein TransportSequence Homology, Amino AcidTumor Suppressor ProteinsCaenorhabditis elegans ProteinsDrosophila Proteinsl(2)gl protein, DrosophilaLGL-1 protein, C elegansMyosin Heavy ChainsNMY-2 protein, C eleganspar-2 protein, C elegansPKC-3 proteinProtein Kinase CTumor Suppressor Proteins

Identifiers

PMID21041363
PMCPMC2976283
OpenAlexW2171655106

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.