Evidence map›Paper›PMID 9763424›Full record

ArticleThe Journal of cell biology1998

Small espin: a third actin-bundling protein and potential forked protein ortholog in brush border microvilli.

J R Bartles, L Zheng, A Li, A Wierda, B Chen

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

86 citing papers in PubMed, 147 citations in OpenAlex.

  1. Article
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  8. Review
  9. Article
  10. Review
  11. Review
  12. Building the brush border, one microvillus at a time.Current opinion in cell biology · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. E3 ubiquitin ligase ASB17 is required for spermiation in mice.Translational andrology and urology · 2021
    Article
  19. Article
  20. Article

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

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

5 authors at 1 institution in 1 country.

J R BartlesDepartment of Cell and Molecular Biology, Northwestern University Medical School, Chicago, Illinois 60611, USA. j-bartles@nwu.edu
L Zheng
A Li
A Wierda
B Chen
Northwestern University · US

Funding

Enhanced Access to HIV Care for Drug Users in San Juan, Puerto RicoR01DA035280 · NIDA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI METSCH, LISA R, SANTANA-BAGUR, JORGE L. · 2013 to 2017
$9.5M
ESPIN AND ECTOPLASMIC SPECIALIZATIONK02HD001210 · NICHD · NORTHWESTERN UNIVERSITY · PI BARTLES, JAMES R · 1998 to 2002
$193k
ESPIN AND THE ECTOPLASMIC SPECIALIZATIONR01HD035280 · NICHD · NORTHWESTERN UNIVERSITY · PI BARTLES, JAMES R · 1997 to 2000
$150k
NICHD NIH HHS K02 HD01210NICHD NIH HHS R01 HD35280NIDA NIH HHS R01 DA035280
6 · The paper itself

Abstract

An approximately 30-kD isoform of the actin-binding/ bundling protein espin has been discovered in the brush borders of absorptive epithelial cells in rat intestine and kidney. Small espin is identical in sequence to the COOH terminus of the larger ( approximately 110-kD) espin isoform identified in the actin bundles of Sertoli cell-spermatid junctional plaques (Bartles, J.R., A. Wierda, and L. Zheng. 1996. J. Cell Sci. 109:1229-1239), but it contains two unique peptides at its NH2 terminus. Small espin was localized to the parallel actin bundles of brush border microvilli, resisted extraction with Triton X-100, and accumulated in the brush border during enterocyte differentiation/migration along the crypt-villus axis in adults. In transfected BHK fibroblasts, green fluorescent protein-small espin decorated F-actin-containing fibers and appeared to elicit their accumulation and/or bundling. Recombinant small espin bound to skeletal muscle and nonmuscle F-actin with high affinity (Kd = 150 and 50 nM) and cross-linked the filaments into bundles. Sedimentation, gel filtration, and circular dichroism analyses suggested that recombinant small espin was a monomer with an asymmetrical shape and a high percentage of alpha-helix. Deletion mutagenesis suggested that small espin contained two actin-binding sites in its COOH-terminal 116-amino acid peptide and that the NH2-terminal half of its forked homology peptide was necessary for bundling activity.

Indexed as

ActinsAmino Acid SequenceAnimalsBase SequenceBinding SitesCell LineCricetinaeGene LibraryGreen Fluorescent ProteinsIntestinal MucosaKidneyLuminescent ProteinsMicrofilament ProteinsMicrovilliMolecular Sequence DataMutagenesisActinsespin protein, mouseGreen Fluorescent ProteinsLuminescent ProteinsMicrofilament ProteinsRecombinant Fusion Proteins

Identifiers

PMID9763424
PMCPMC2132824
OpenAlexW2121858951

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.