Evidence map›Paper›PMID 36946995›Full record

ArticleThe Journal of cell biology2023

The meiotic LINC complex component KASH5 is an activating adaptor for cytoplasmic dynein.

Kirsten E L Garner, Anna Salter, Clinton K Lau, Manickam Gurusaran, Cécile M Villemant, Elizabeth P Granger, Gavin McNee, Philip G Woodman, Owen R Davies, Brian E Burke and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. The Nemp1-Nesprin complex mediates cellular responses to matrix mechanics.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Heterochromatin in plant meiosis.Nucleus (Austin, Tex.) · 2024
    Review
  12. Review
  13. Review
  14. Article
  15. 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

11 authors at 4 institutions in 2 countries.

Kirsten E L Garner *School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester , Manchester, UK.ORCID 0000-0002-9792-4239
Anna Salter *School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester , Manchester, UK.ORCID 0000-0001-9429-6081
Clinton K LauMRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge Biomedical Campus , Cambridge, UK.ORCID 0000-0003-1083-2989
Manickam GurusaranWellcome Centre for Cell Biology, Institute of Cell Biology, University of Edinburgh , Edinburgh, UK.ORCID 0000-0002-6603-3118
Cécile M VillemantSchool of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester , Manchester, UK.ORCID 0000-0002-9682-3778
Elizabeth P GrangerSchool of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester , Manchester, UK.ORCID 0000-0002-0405-2794
Gavin McNeeSchool of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester , Manchester, UK.ORCID 0000-0003-4504-0404
Philip G WoodmanSchool of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester , Manchester, UK.ORCID 0000-0001-9497-1235
Owen R DaviesWellcome Centre for Cell Biology, Institute of Cell Biology, University of Edinburgh , Edinburgh, UK.ORCID 0000-0002-3806-5403
Brian E Burke *A*STAR Institute of Medical Biology , Singapore, Singapore.ORCID 0000-0002-6887-7154
Victoria J Allan *School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester , Manchester, UK.ORCID 0000-0003-4583-0836
University of Manchester · GBAgency for Science, Technology and Research · SGWellcome Centre for Cell Biology · GBMRC Laboratory of Molecular Biology · GB

Funding

Biotechnology and Biological Sciences Research Council BB/N006933/1Medical Research Council MC_UP_A025_1011Wellcome TrustWellcome Trust WT210711
6 · The paper itself

Abstract

Cytoplasmic dynein-driven movement of chromosomes during prophase I of mammalian meiosis is essential for synapsis and genetic exchange. Dynein connects to chromosome telomeres via KASH5 and SUN1 or SUN2, which together span the nuclear envelope. Here, we show that KASH5 promotes dynein motility in vitro, and cytosolic KASH5 inhibits dynein's interphase functions. KASH5 interacts with a dynein light intermediate chain (DYNC1LI1 or DYNC1LI2) via a conserved helix in the LIC C-terminal, and this region is also needed for dynein's recruitment to other cellular membranes. KASH5's N-terminal EF-hands are essential as the interaction with dynein is disrupted by mutation of key calcium-binding residues, although it is not regulated by cellular calcium levels. Dynein can be recruited to KASH5 at the nuclear envelope independently of dynactin, while LIS1 is essential for dynactin incorporation into the KASH5-dynein complex. Altogether, we show that the transmembrane protein KASH5 is an activating adaptor for dynein and shed light on the hierarchy of assembly of KASH5-dynein-dynactin complexes.

Indexed as

Cell Cycle ProteinsCytoplasmic DyneinsDynactin ComplexMicrotubule-Associated ProteinsAnimalsCalciumMammalsNuclear EnvelopeTelomereCalciumCell Cycle ProteinsCytoplasmic DyneinsDynactin ComplexMicrotubule-Associated Proteins

Identifiers

PMID36946995
PMCPMC10071310
OpenAlexW4353015072

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.