Evidence map›Paper›PMID 39085203›Full record

ArticleCell death & disease2024

Eg5 UFMylation promotes spindle organization during mitosis.

Guangxu Li, Yuanjiang Huang, Wenbo Han, Liyi Wei, Hongjing Huang, Yingbao Zhu, Qiao Xiao, Zujia Wang, Wen Huang, Ranhui Duan

Abstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Kinesin Spindle Protein (KIF11) in Mitosis and Cancer.International journal of molecular sciences · 2025
    Review
  9. Review
  10. 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

10 authors.

Guangxu Li *Furong Laboratory, Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, China.ORCID 0009-0006-7474-7141
Yuanjiang Huang *Furong Laboratory, Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, China.
Wenbo HanFurong Laboratory, Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, China.
Liyi WeiFurong Laboratory, Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, China.
Hongjing HuangFurong Laboratory, Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, China.
Yingbao ZhuFurong Laboratory, Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, China.
Qiao XiaoFurong Laboratory, Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, China.
Zujia WangFurong Laboratory, Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, China.
Wen HuangFurong Laboratory, Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, China.
Ranhui DuanFurong Laboratory, Center for Medical Genetics, School of Life Sciences, Central South University, Changsha, China. duanranhui@sklmg.edu.cn.ORCID 0000-0001-7117-4487

Funding

Hunan Provincial Science and Technology Department (Department of Science and Technology of Hunan Province) 2019SK1010National Natural Science Foundation of China (National Science Foundation of China) 82071273National Natural Science Foundation of China (National Science Foundation of China) 82101958National Natural Science Foundation of China (National Science Foundation of China) 82271906
6 · The paper itself

Abstract

UFMylation is a highly conserved ubiquitin-like post-translational modification that catalyzes the covalent linkage of UFM1 to its target proteins. This modification plays a critical role in the maintenance of endoplasmic reticulum proteostasis, DNA damage response, autophagy, and transcriptional regulation. Mutations in UFM1, as well as in its specific E1 enzyme UBA5 and E2 enzyme UFC1, have been genetically linked to microcephaly. Our previous research unveiled the important role of UFMylation in regulating mitosis. However, the underlying mechanisms have remained unclear due to the limited identification of substrates. In this study, we identified Eg5, a motor protein crucial for mitotic spindle assembly and maintenance, as a novel substrate for UFMylation and identified Lys564 as the crucial UFMylation site. UFMylation did not alter its transcriptional level, phosphorylation level, or protein stability, but affected the mono-ubiquitination of Eg5. During mitosis, Eg5 and UFM1 co-localize at the centrosome and spindle apparatus, and defective UFMylation leads to diminished spindle localization of Eg5. Notably, the UFMylation-defective Eg5 mutant (K564R) exhibited shorter spindles, metaphase arrest, spindle checkpoint activation, and a failure of cell division in HeLa cells. Overall, Eg5 UFMylation is essential for proper spindle organization, mitotic progression, and cell proliferation.

Indexed as

KinesinsMitosisSpindle ApparatusUbiquitinationCentrosomeHEK293 CellsHeLa CellsHumansProtein Processing, Post-TranslationalProteinsUbiquitin-Activating EnzymesKIF11 protein, humanKinesinsProteinsUBA5 protein, humanUbiquitin-Activating EnzymesUFM1 protein, human

Identifiers

PMID39085203
PMCPMC11291904

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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.