Evidence map›Paper›PMID 24030547›Full record

ArticleHuman molecular genetics2014

LIS1 controls mitosis and mitotic spindle organization via the LIS1-NDEL1-dynein complex.

Hyang Mi Moon, Yong Ha Youn, Hayley Pemble, Jessica Yingling, Torsten Wittmann, Anthony Wynshaw-Boris

Open access · bronzeAbstract read
In one paragraph

Article in Human molecular genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

59 citing papers in PubMed, 104 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Understanding the Molecular Basis of Miller-Dieker Syndrome.International journal of molecular sciences · 2025
    Review
  5. CCSer2 gates dynein activity at the cell periphery.The Journal of cell biology · 2025
    Article
  6. Article
  7. Article
  8. Nde1 Promotes Lis1 Binding to Full-Length Autoinhibited Human Dynein-1.bioRxiv : the preprint server for biology · 2025
    Article
  9. CCSer2 gates dynein activity at the cell periphery.bioRxiv : the preprint server for biology · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Nde1 Promotes Lis1-Mediated Activation of Dynein.bioRxiv : the preprint server for biology · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Ndel1 modulates dynein activation in two distinct ways.bioRxiv : the preprint server for biology · 2023
    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

6 authors at 3 institutions in 2 countries.

Hyang Mi MoonDepartment of Pediatrics, Institute for Human Genetics.
Yong Ha Youn
Hayley Pemble
Jessica Yingling
Torsten Wittmann
Anthony Wynshaw-Boris
Broad Center · USInstitute of Biomedical Science · GBUniversity of California, San Diego · US

Funding

Genetic Analysis of LIS1 Function in the MouseR01NS041030 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WYNSHAW-BORIS, ANTHONY J. · 2002 to 2009
$3.1M
Genetic Regulation of Neuronal MigrationR01HD047380 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WYNSHAW-BORIS, ANTHONY J. · 2005 to 2009
$1.2M
NICHD NIH HHS R01 HD047380NINDS NIH HHS R01 NS41030
6 · The paper itself

Abstract

Heterozygous LIS1 mutations are responsible for the human neuronal migration disorder lissencephaly. Mitotic functions of LIS1 have been suggested from many organisms throughout evolution. However, the cellular functions of LIS1 at distinct intracellular compartments such as the centrosome and the cell cortex have not been well defined especially during mitotic cell division. Here, we used detailed cellular approaches and time-lapse live cell imaging of mitosis from Lis1 mutant mouse embryonic fibroblasts to reveal critical roles of LIS1 in mitotic spindle regulation. We found that LIS1 is required for the tight control of chromosome congression and segregation to dictate kinetochore-microtubule (MT) interactions and anaphase progression. In addition, LIS1 is essential for the establishment of mitotic spindle pole integrity by maintaining normal centrosome number. Moreover, LIS1 plays crucial roles in mitotic spindle orientation by increasing the density of astral MT plus-end movements toward the cell cortex, which enhances cortical targeting of LIS1-dynein complex. Overexpression of NDEL1-dynein and MT stabilization rescues spindle orientation defects in Lis1 mutants, demonstrating that mouse LIS1 acts via the LIS1-NDEL1-dynein complex to regulate astral MT plus-ends dynamics and establish proper contacts of MTs with the cell cortex to ensure precise cell division.

Indexed as

Mitosis1-Alkyl-2-acetylglycerophosphocholine EsteraseAnimalsCarrier ProteinsCells, CulturedCentrosomeCerebral CortexChromosome SegregationDyneinsHEK293 CellsHumansLissencephalyMiceMicrotubule-Associated ProteinsMicrotubulesMutation1-Alkyl-2-acetylglycerophosphocholine EsteraseCarrier ProteinsDyneinsMicrotubule-Associated ProteinsNdel1 protein, mousePafah1b1 protein, mouse

Identifiers

PMID24030547
PMCPMC3869364
OpenAlexW2161458853

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.