Evidence map›Paper›PMID 35686621›Full record

ArticleThe EMBO journal2022

Precise control of microtubule disassembly in living cells.

Grace Y Liu, Shiau-Chi Chen, Gang-Hui Lee, Kritika Shaiv, Pin-Yu Chen, Hsuan Cheng, Shi-Rong Hong, Wen-Ting Yang, Shih-Han Huang, Ya-Chu Chang and 7 more

Open access · hybridAbstract read
In one paragraph

Article in The EMBO journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 37 citations in OpenAlex.

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  11. A review of mirvetuximab soravtansine-gynx in folate receptor alpha-expressing platinum-resistant ovarian cancer.American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists · 2025
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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

17 authors at 2 institutions in 1 country.

Grace Y Liu *Institute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Shiau-Chi Chen *Institute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Gang-Hui Lee *Department of Physiology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Kritika ShaivInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Pin-Yu ChenInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Hsuan ChengInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Shi-Rong HongInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Wen-Ting YangInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.ORCID 0000-0001-8720-8530
Shih-Han HuangInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Ya-Chu ChangInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Hsien-Chu WangInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Ching-Lin KaoInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Pin-Chiao SunInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Ming-Hong ChaoInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Yian-Ying LeeInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.
Ming-Jer TangDepartment of Physiology, College of Medicine, National Cheng Kung University, Tainan, Taiwan.ORCID 0000-0002-0883-4363
Yu-Chun LinInstitute of Molecular Medicine, National Tsing Hua University, Hsinchu, Taiwan.ORCID 0000-0002-9629-7560
National Tsing Hua University · TWNational Cheng Kung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microtubules tightly regulate various cellular activities. Our understanding of microtubules is largely based on experiments using microtubule-targeting agents, which, however, are insufficient to dissect the dynamic mechanisms of specific microtubule populations, due to their slow effects on the entire pool of microtubules. To overcome this technological limitation, we have used chemo and optogenetics to disassemble specific microtubule subtypes, including tyrosinated microtubules, primary cilia, mitotic spindles, and intercellular bridges, by rapidly recruiting engineered microtubule-cleaving enzymes onto target microtubules in a reversible manner. Using this approach, we show that acute microtubule disassembly swiftly halts vesicular trafficking and lysosomal dynamics. It also immediately triggers Golgi and ER reorganization and slows the fusion/fission of mitochondria without affecting mitochondrial membrane potential. In addition, cell rigidity is increased after microtubule disruption owing to increased contractile stress fibers. Microtubule disruption furthermore prevents cell division, but does not cause cell death during interphase. Overall, the reported tools facilitate detailed analysis of how microtubules precisely regulate cellular architecture and functions.

Indexed as

MicrotubulesSpindle ApparatusInterphaseintercellular bridgemicrotubulemitotic spindleprimary ciliumspastin

Identifiers

PMID35686621
PMCPMC9340485
OpenAlexW4281735145

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.