Evidence map›Paper›PMID 19638346›Full record

ArticleThe Journal of biological chemistry2009

Activating mutations of the TRPML1 channel revealed by proline-scanning mutagenesis.

Xian-ping Dong, Xiang Wang, Dongbiao Shen, Su Chen, Meiling Liu, Yanbin Wang, Eric Mills, Xiping Cheng, Markus Delling, Haoxing Xu

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
6.1field-weighted citation impact, top 3% 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

73 citing papers in PubMed, 130 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. TRPML1 gating modulation by allosteric mutations and lipids.bioRxiv : the preprint server for biology · 2024
    Article
  6. Article
  7. The ion channels of endomembranes.Physiological reviews · 2024
    Review
  8. Review
  9. Review
  10. Article
  11. A Structural Overview of TRPML1 and the TRPML Family.Handbook of experimental pharmacology · 2023
    Article
  12. Article
  13. Lysosomal KEMBO reports · 2022
    Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Lysosomal TRPML1 Channel: Implications in Cardiovascular and Kidney Diseases.Advances in experimental medicine and biology · 2021
    Article
  19. Review
  20. A lysosomal KScientific reports · 2020
    Article

13 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

10 authors at 2 institutions in 1 country.

Xian-ping DongDepartment of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Xiang Wang
Dongbiao Shen
Su Chen
Meiling Liu
Yanbin Wang
Eric Mills
Xiping Cheng
Markus Delling
Haoxing Xu
University of Michigan–Ann Arbor · USBoston Children's Hospital · US

Funding

The Mucolipin TRP Ion ChannelsR01NS062792 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI XU, HAOXING · 2009 to 2018
$3.3M
NINDS NIH HHS NS062792NINDS NIH HHS R01 NS062792
6 · The paper itself

Abstract

The mucolipin TRP (TRPML) proteins are a family of endolysosomal cation channels with genetically established importance in humans and rodent. Mutations of human TRPML1 cause type IV mucolipidosis, a devastating pediatric neurodegenerative disease. Our recent electrophysiological studies revealed that, although a TRPML1-mediated current can only be recorded in late endosome and lysosome (LEL) using the lysosome patch clamp technique, a proline substitution in TRPML1 (TRPML1(V432P)) results in a large whole cell current. Thus, it remains unknown whether the large TRPML1(V432P)-mediated current results from an increased surface expression (trafficking), elevated channel activity (gating), or both. Here we performed systemic Pro substitutions in a region previously implicated in the gating of various 6 transmembrane cation channels. We found that several Pro substitutions displayed gain-of-function (GOF) constitutive activities at both the plasma membrane (PM) and endolysosomal membranes. Although wild-type TRPML1 and non-GOF Pro substitutions localized exclusively in LEL and were barely detectable in the PM, the GOF mutations with high constitutive activities were not restricted to LEL compartments, and most significantly, exhibited significant surface expression. Because lysosomal exocytosis is Ca(2+)-dependent, constitutive Ca(2+) permeability due to Pro substitutions may have resulted in stimulus-independent intralysosomal Ca(2+) release, hence the surface expression and whole cell current of TRPML1. Indeed, surface staining of lysosome-associated membrane protein-1 (Lamp-1) was dramatically increased in cells expressing GOF TRPML1 channels. We conclude that TRPML1 is an inwardly rectifying, proton-impermeable, Ca(2+) and Fe(2+)/Mn(2+) dually permeable cation channel that may be gated by unidentified cellular mechanisms through a conformational change in the cytoplasmic face of the transmembrane 5 (TM5). Furthermore, activation of TRPML1 in LEL may lead to the appearance of TRPML1 proteins at the PM.

Indexed as

Amino Acid SequenceAmino Acid SubstitutionCalciumCells, CulturedElectrophysiologyExocytosisHumansKidneyLysosomesManganeseMolecular Sequence DataMutagenesisMutationProlineSequence Homology, Amino AcidTransient Receptor Potential ChannelsCalciumManganeseMCOLN1 protein, humanProlineTransient Receptor Potential ChannelsTRPM Cation Channels

Identifiers

PMID19638346
PMCPMC2797275
OpenAlexW2065524119

What OpenQuestion holds

Textmetadata
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.