Evidence map›Paper›PMID 28325809›Full record

ArticleThe Journal of cell biology2017

The Rab7 effector PLEKHM1 binds Arl8b to promote cargo traffic to lysosomes.

Rituraj Marwaha, Subhash B Arya, Divya Jagga, Harmeet Kaur, Amit Tuli, Mahak Sharma

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
8.3field-weighted citation impact, top 1% 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

88 citing papers in PubMed, 162 citations in OpenAlex.

  1. Article
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  4. Late Endosome Transport by RILP-RAB7A Promotes Dendrite Arborization Independently of Degradation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  5. Review
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  8. Late endosome transport by RILP-RAB7A promotes dendrite arborization.bioRxiv : the preprint server for biology · 2025
    Article
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  11. Review
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  15. Article
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28 more citing papers are in PubMed but not listed here.

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 2 institutions in 1 country.

Rituraj MarwahaDepartment of Biological Sciences, Indian Institute of Science Education and Research, Mohali, Punjab 140306, India.
Subhash B AryaDivision of Cell Biology and Immunology, Council of Scientific and Industrial Research, Institute of Microbial Technology, Chandigarh 160036, India.
Divya JaggaDivision of Cell Biology and Immunology, Council of Scientific and Industrial Research, Institute of Microbial Technology, Chandigarh 160036, India.
Harmeet KaurDivision of Cell Biology and Immunology, Council of Scientific and Industrial Research, Institute of Microbial Technology, Chandigarh 160036, India.
Amit TuliDivision of Cell Biology and Immunology, Council of Scientific and Industrial Research, Institute of Microbial Technology, Chandigarh 160036, India atuli@imtech.res.in msharma@iisermohali.ac.in.ORCID 0000-0001-5476-4127
Mahak SharmaDepartment of Biological Sciences, Indian Institute of Science Education and Research, Mohali, Punjab 140306, India atuli@imtech.res.in msharma@iisermohali.ac.in.ORCID 0000-0002-4117-4790
Institute of Microbial Technology · INIndian Institute of Science Education and Research Mohali · IN

Funding

DBT-Wellcome Trust India Alliance IA/I/12/1/500523DBT-Wellcome Trust India Alliance IA/I/14/2/501543Wellcome Trust
6 · The paper itself

Abstract

Endocytic, autophagic, and phagocytic vesicles move on microtubule tracks to fuse with lysosomes. Small GTPases, such as Rab7 and Arl8b, recruit their downstream effectors to mediate this transport and fusion. However, the potential cross talk between these two GTPases is unclear. Here, we show that the Rab7 effector PLEKHM1 simultaneously binds Rab7 and Arl8b, bringing about clustering and fusion of late endosomes and lysosomes. We show that the N-terminal RUN domain of PLEKHM1 is necessary and sufficient for interaction with Arl8b and its subsequent localization to lysosomes. Notably, we also demonstrate that Arl8b mediates recruitment of HOPS complex to PLEKHM1-positive vesicle contact sites. Consequently, Arl8b binding to PLEKHM1 is required for its function in delivery and, therefore, degradation of endocytic and autophagic cargo in lysosomes. Finally, we also show that PLEKHM1 competes with SKIP for Arl8b binding, which dictates lysosome positioning. These findings suggest that Arl8b, along with its effectors, orchestrates lysosomal transport and fusion.

Indexed as

Adaptor Proteins, Signal TransducingADP-Ribosylation FactorsAnimalsAutophagyBiological TransportCell LineCell Line, TumorEndosomesHEK293 CellsHeLa CellsHumansLysosomesMembrane GlycoproteinsMicrotubulesProtein Bindingrab7 GTP-Binding ProteinsAdaptor Proteins, Signal TransducingADP-Ribosylation FactorsMembrane Glycoproteinsrab7 GTP-Binding Proteinsrab7 GTP-binding proteins, humanrab GTP-Binding Proteins

Identifiers

PMID28325809
PMCPMC5379943
OpenAlexW2603101815

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.