Evidence map›Paper›PMID 30567713›Full record

ArticleThe Journal of cell biology2019

Detyrosinated microtubules spatially constrain lysosomes facilitating lysosome-autophagosome fusion.

Nitin Mohan, Elena M Sorokina, Ione Vilanova Verdeny, Angel Sandoval Alvarez, Melike Lakadamyali

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In one paragraph

Article in The Journal of cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing 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

51 citing papers in PubMed.

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  6. Peptide-based covalent inhibitor of tubulin detyrosination promotes mesenchymal-to-epithelial transition in lung cancer cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
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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

5 authors.

Nitin MohanDepartment of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Elena M SorokinaDepartment of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0003-2079-869X
Ione Vilanova VerdenyInstitut de Ciencies Fotoniques, The Barcelona Institute of Science and Technology, Barcelona, Spain.
Angel Sandoval AlvarezInstitut de Ciencies Fotoniques, The Barcelona Institute of Science and Technology, Barcelona, Spain.
Melike LakadamyaliDepartment of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA melikel@pennmedicine.upenn.edu.ORCID 0000-0002-7524-6414

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microtubule post-translational modifications impart functional diversity to microtubules by affecting their dynamics, organization, and interaction with proteins. Using super-resolution microscopy, we show that only a small subpopulation of microtubules are detyrosinated in epithelial cells, while acetylated and tyrosinated microtubules comprise the majority of all microtubules. Surprisingly, lysosomes are enriched by approximately threefold on detyrosinated microtubules. Further, their motility on detyrosinated microtubules is impaired, showing shorter runs and more frequent and longer pauses. Lysosome enrichment is mediated through a kinesin-1-dependent mechanism, since knocking down this motor abolishes enrichment. Finally, correlative live-cell and super-resolution microscopy showed that lysosomes interact with autophagosomes on detyrosinated microtubules. Removal of detyrosinated microtubules or knockdown of kinesin-1 leads to a decrease in the percentage of autolysosomes, a fusion intermediate of autophagosomes and lysosomes. Taken together, our data reveal a new role of detyrosinated microtubules as hubs that spatially concentrate lysosomes on a small subset of microtubules and facilitate their interaction and fusion with autophagosomes to initiate autophagy.

Indexed as

Membrane FusionProtein Processing, Post-TranslationalAcetylationAnimalsAutophagosomesCell LineChlorocebus aethiopsEpithelial CellsKidneyKinesinsLysosomesMicrotubulesTubulinTyrosineKinesinsTubulinTyrosine

Identifiers

PMID30567713
PMCPMC6363446

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.