Evidence map›Paper›PMID 39504124›Full record

ArticleeLife2024

Functional implications of the exon 9 splice insert in GluK1 kainate receptors.

Surbhi Dhingra, Prachi M Chopade, Rajesh Vinnakota, Janesh Kumar

Abstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Structure and gating of kainate receptors.Frontiers in pharmacology · 2025
    Review
  3. 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

4 authors.

Surbhi DhingraLaboratory of Membrane Protein Biology, National Centre for Cell Science, Pune, India.ORCID https://orcid.org/0000-0003-4349-3215
Prachi M Chopade *Laboratory of Membrane Protein Biology, National Centre for Cell Science, Pune, India.ORCID https://orcid.org/0000-0001-5394-1136
Rajesh Vinnakota *Laboratory of Membrane Protein Biology, National Centre for Cell Science, Pune, India.ORCID https://orcid.org/0000-0002-2354-5105
Janesh KumarLaboratory of Membrane Protein Biology, National Centre for Cell Science, Pune, India.ORCID https://orcid.org/0000-0003-0767-3788

Funding

Department of Science and Technology, Ministry of Science and Technology, India CRG/2020/003971
6 · The paper itself

Abstract

Kainate receptors are key modulators of synaptic transmission and plasticity in the central nervous system. Different kainate receptor isoforms with distinct spatiotemporal expressions have been identified in the brain. The GluK1-1 splice variant receptors, which are abundant in the adult brain, have an extra fifteen amino acids inserted in the amino-terminal domain (ATD) of the receptor resulting from alternative splicing of exon 9. However, the functional implications of this post-transcriptional modification are not yet clear. We employed a multi-pronged approach using cryogenic electron microscopy, electrophysiology, and other biophysical and biochemical tools to understand the structural and functional impact of this splice insert in the extracellular domain of GluK1 receptors. Our study reveals that the splice insert alters the key gating properties of GluK1 receptors and their modulation by the cognate auxiliary Neuropilin and tolloid-like (Neto) proteins 1 and 2. Mutational analysis identified the role of crucial splice residues that influence receptor properties and their modulation. Furthermore, the cryoEM structure of the variant shows that the presence of exon 9 in GluK1 does not affect the receptor architecture or domain arrangement in the desensitized state. Our study thus provides the first detailed structural and functional characterization of GluK1-1a receptors, highlighting the role of the splice insert in modulating receptor properties and their modulation.

Indexed as

Alternative SplicingExonsKainic Acid ReceptorsAnimalsCryoelectron MicroscopyHEK293 CellsHumansProtein IsoformsKainic Acid ReceptorsProtein Isoformsalternative splicingCryo-EMelectrophysiologykainate receptorsmolecular biophysicsratstructural biology

Identifiers

PMID39504124
PMCPMC11540303

What Socratic 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 Socratic graph.