Evidence map›Paper›PMID 23569209›Full record

ArticleThe Journal of biological chemistry2013

A single divergent exon inhibits ankyrin-B association with the plasma membrane.

Meng He, Wei-Chou Tseng, Vann Bennett

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
  2. Review
  3. Ankyrin-B is lipid-modified byFrontiers in physiology · 2023
    Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Neurodevelopmental mutation of giant ankyrin-G disrupts a core mechanism for axon initial segment assembly.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Novel Variant in theCirculation. Cardiovascular genetics · 2017
    Article
  15. Article
  16. Article
  17. Giant ankyrin-G stabilizes somatodendritic GABAergic synapses through opposing endocytosis of GABAA receptors.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  18. Article
  19. Article
  20. 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

3 authors.

Meng HeDepartment of Pharmacology and Cancer Biology, Duke University, Medical Center, Durham, North Carolina 27710, USA.
Wei-Chou Tseng
Vann Bennett

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

Vertebrate ankyrin-B and ankyrin-G exhibit divergent subcellular localization and function despite their high sequence and structural similarity and common origin from a single ancestral gene at the onset of chordate evolution. Previous studies of ankyrin family diversity have focused on the C-terminal regulatory domain. Here, we identify an ankyrin-B-specific linker peptide connecting the ankyrin repeat domain to the ZU52-UPA module that inhibits binding of ankyrin-B to membrane protein partners E-cadherin and neurofascin 186 and prevents association of ankyrin-B with epithelial lateral membranes as well as neuronal plasma membranes. The residues of the ankyrin-B linker required for autoinhibition are encoded by a small exon that is highly divergent between ankyrin family members but conserved in the ankyrin-B lineage. We show that the ankyrin-B linker suppresses activity of the ANK repeat domain through an intramolecular interaction, likely with a groove on the surface of the ANK repeat solenoid, thereby regulating the affinities between ankyrin-B and its binding partners. These results provide a simple evolutionary explanation for how ankyrin-B and ankyrin-G have acquired striking differences in their plasma membrane association while maintaining overall high levels of sequence similarity.

Indexed as

AnimalsAnkyrin RepeatAnkyrinsCadherinsCell Adhesion MoleculesCell MembraneDogsExonsHEK293 CellsHumansMadin Darby Canine Kidney CellsNerve Growth FactorsNeuronsProtein BindingANK2 protein, humanANK3 protein, humanAnkyrinsCadherinsCell Adhesion MoleculesNerve Growth FactorsNFASC protein, humanAnkyrin DiversityAutoinhibitionEpithelial CellEvolutionIntramolecular InteractionNeuronsPlasma MembraneTransfection

Identifiers

PMID23569209
PMCPMC3663501

What OpenQuestion holds

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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.