Evidence map›Paper›PMID 21169557›Full record

ArticleMolecular biology of the cell2011

Recruitment of dynein to late endosomes and lysosomes through light intermediate chains.

Serena C Tan, Julian Scherer, Richard B Vallee

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

54 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
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  11. Dynein Is Required for Rab7-Dependent Endosome Maturation, Retrograde Dendritic Transport, and Degradation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
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  15. The conserved autoimmune-disease risk geneProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Inositol hexakisphosphate kinase 3 promotes focal adhesion turnover via interactions with dynein intermediate chain 2.Proceedings of the National Academy of Sciences of the United States of America · 2019
    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

3 authors at 1 institution in 1 country.

Serena C TanDepartment of Pathology, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
Julian Scherer
Richard B Vallee
Columbia University · US

Funding

MOLECULAR GENETICS OF CYTOPLASMIC DYNEINR37GM047434 · NIGMS · WORCESTER FOUNDATION FOR BIOMEDICAL RES · PI VALLEE, RICHARD BERT · 1996 to 2006
$3.5M
MOLECULAR GENETICS OF CYTOPLASMIC DYNEINR01GM047434 · NIGMS · WORCESTER FOUNDATION FOR BIOMEDICAL RES · PI VALLEE, RICHARD BERT · 1992 to 2010
$2.6M
NIGMS NIH HHS GM47434NIGMS NIH HHS R01 GM047434NIGMS NIH HHS R37 GM047434
6 · The paper itself

Abstract

Cytoplasmic dynein is involved in a wide range of cellular processes, but how it is regulated and how it recognizes an extremely wide range of cargo are incompletely understood. The dynein light intermediate chains, LIC1 and LIC2 (DYNC1LI1 and DYNC1LI2, respectively), have been implicated in cargo binding, but their full range of functions is unknown. Using LIC isoform-specific antibodies, we report the first characterization of their subcellular distribution and identify a specific association with elements of the late endocytic pathway, but not other vesicular compartments. LIC1 and LIC2 RNA interference (RNAi) each specifically disrupts the distribution of lysosomes and late endosomes. Stimulation of dynein-mediated late-endosomal transport by the Rab7-interacting lysosomal protein (RILP) is reversed by LIC1 RNAi, which displaces dynein, but not dynactin, from these structures. Conversely, expression of ΔN-RILP or the dynactin subunit dynamitin each fails to displace dynein, but not dynactin. Thus, using a variety of complementary approaches, our results indicate a novel specific role for the LICs in dynein recruitment to components of the late endocytic pathway.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCarrier ProteinsCytoplasmic DyneinsDynactin ComplexEndosomesGene Knockdown TechniquesHeLa CellsHumansLysosomal-Associated Membrane Protein 1LysosomesMicrotubule-Associated ProteinsMicrotubulesMolecular Motor ProteinsProtein Bindingrab7 GTP-Binding ProteinsAdaptor Proteins, Signal TransducingCarrier ProteinsCytoplasmic DyneinsDCTN2 protein, humanDynactin ComplexDYNC1LI1 protein, humanDYNC1LI2 protein, humanLysosomal-Associated Membrane Protein 1Microtubule-Associated ProteinsMolecular Motor Proteinsrab7 GTP-Binding Proteinsrab7 GTP-binding proteins, humanrab7 GTP-binding proteins, ratrab GTP-Binding ProteinsRILP protein, human

Identifiers

PMID21169557
PMCPMC3038645
OpenAlexW2017228257

What OpenQuestion holds

Textmetadata
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.