Evidence map›Paper›PMID 22308397›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Kinesin-2 family in vertebrate ciliogenesis.

Chengtian Zhao, Yoshihiro Omori, Katarzyna Brodowska, Peter Kovach, Jarema Malicki

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

52 citing papers in PubMed, 91 citations in OpenAlex.

  1. Article
  2. Kinesins inOpen biology · 2025
    Review
  3. Article
  4. Article
  5. Review
  6. Involvement of kinesins in skeletal dysplasia: a review.American journal of physiology. Cell physiology · 2024
    Review
  7. Article
  8. Review
  9. Review
  10. Cilia regulate meiotic recombination in zebrafish.Journal of molecular cell biology · 2022
    Article
  11. Article
  12. Article
  13. Photoreceptor Compartment-Specific TULP1 Interactomes.International journal of molecular sciences · 2021
    Article
  14. Review
  15. The developmental biology of kinesins.Developmental biology · 2021
    Review
  16. Article
  17. Article
  18. Article
  19. Cilia in the developing zebrafish ear.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Review
  20. 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

5 authors at 1 institution in 1 country.

Chengtian ZhaoDivision of Craniofacial and Molecular Genetics and Program in Genetics, Sackler School of Graduate Biomedical Studies, Tufts University, Boston, MA 02111, USA.
Yoshihiro Omori
Katarzyna Brodowska
Peter Kovach
Jarema Malicki
Tufts University · US

Funding

CILIA IN EYE DEVELOPMENT AND DISEASER01EY018176 · NEI · UNIVERSITY OF SHEFFIELD · PI MALICKI, JAREMA · 2008 to 2014
$2.4M
GENETIC ANALYSIS OF PHOTORECEPTOR DIFFERENTIATIONR01EY016859 · NEI · TUFTS UNIVERSITY BOSTON · PI MALICKI, JAREMA · 2005 to 2010
$2.0M
NEI NIH HHS R01 EY016859NEI NIH HHS R01 EY018176Wellcome Trust WT 077047/Z/05/Z
6 · The paper itself

Abstract

The differentiation of cilia is mediated by kinesin-driven transport. As the function of kinesins in vertebrate ciliogenesis is poorly characterized, we decided to determine the role of kinesin-2 family motors--heterotrimeric kinesin-II and the homodimeric Kif17 kinesin--in zebrafish cilia. We report that kif17 is largely dispensable for ciliogenesis; kif17 homozygous mutant animals are viable and display subtle morphological defects of olfactory cilia only. In contrast to that, the kif3b gene, encoding a heterotrimeric kinesin subunit, is necessary for cilia differentiation in most tissues, although exceptions exist, and include photoreceptors and a subset of hair cells. Cilia of these cell types persist even in kif3b/kif17 double mutants. Although we have not observed a functional redundancy of kif3b and kif17, kif17 is able to substitute for kif3b in some cilia. In contrast to kif3b/kif17 double mutants, simultaneous interference with kif3b and kif3c leads to the complete loss of photoreceptor and hair cell cilia, revealing redundancy of function. This is in agreement with the idea that Kif3b and Kif3c motor subunits form complexes with Kif3a, but not with each other. Interestingly, kif3b mutant photoreceptor cilia differentiate with a delay, suggesting that kif3c, although redundant with kif3b at later stages of differentiation, is not active early in photoreceptor ciliogenesis. Consistent with that, the overexpression of kif3c in kif3b mutants rescues early photoreceptor cilia defects. These data reveal unexpected diversity of functional relationships between vertebrate ciliary kinesins, and show that the repertoire of kinesin motors changes in some cilia during their differentiation.

Indexed as

CiliaAnimalsBase SequenceDNA PrimersHomozygoteImmunohistochemistryKinesinsMutationPolymerase Chain ReactionZebrafishDNA PrimersKinesins

Identifiers

PMID22308397
PMCPMC3289367
OpenAlexW2061604906

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.