A novel anxiety-associated SNP identified in LYNX2 (LYPD1) is associated with decreased protein binding to nicotinic acetylcholine receptors

A polymorphism in LYNX2, which codes for an inhibitory modulator of nicotinic acetylcholine receptors, has the potential to lead to sensitized nicotinic receptor activity in anxiety-related circuits. The LYNX2 protein has been shown to bind to multiple nicotinic acetylcholine receptor subtypes, including α4β2, α7, and α3β4 subtypes, each of which have been shown to be involved in affective behaviors. This work suggests that a subpopulation of individuals harboring a deleterious mutation in LYNX2 may predispose them to anxiety through abnormal nicotinic receptor control. In the future, this work may lead to the development of a biomarker for anxiety or a diagnostic tool for the early detection of individuals with susceptibility to anxiety.

Authors

Institutions

Publication Details

Journal
Frontiers in Behavioral Neuroscience
Published
2024-12-23
DOI
https://doi.org/10.3389/fnbeh.2024.1347543
Citations
2
Primary Topic
Nicotinic Acetylcholine Receptors Study
Type
article
Field-Weighted Citation Impact
0.47

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

A novel anxiety-associated SNP identified in LYNX2 (LYPD1) is associated with decreased protein binding to nicotinic acetylcholine receptors

Talulla B. Palumbo, Krystle J. McLaughlin, Matthew Beatty, Amanda DeGraaf et al.
2 citations
Frontiers in Behavioral Neuroscience
Nicotinic Acetylcholine Receptors Study
0.47
article

A novel anxiety-associated SNP identified in LYNX2 (LYPD1) is associated with decreased protein binding to nicotinic acetylcholine receptors

Talulla B. Palumbo, Krystle J. McLaughlin, Matthew Beatty, Amanda DeGraaf, K. Anderson, Peter Rogu, Wonpil Im, Gabrielle M. Gracias, Katie M. Hoffman, Almut Hupbach, Julie M. Miwa, Wenpeng Cao, Avani V. Pisapati, Xiao Hui Zhang, Mark A. Crenshaw, Hui Sun Lee, Ethan Fisher-Perez
article en
2 citations

Abstract

A polymorphism in LYNX2, which codes for an inhibitory modulator of nicotinic acetylcholine receptors, has the potential to lead to sensitized nicotinic receptor activity in anxiety-related circuits. The LYNX2 protein has been shown to bind to multiple nicotinic acetylcholine receptor subtypes, including α4β2, α7, and α3β4 subtypes, each of which have been shown to be involved in affective behaviors. This work suggests that a subpopulation of individuals harboring a deleterious mutation in LYNX2 may predispose them to anxiety through abnormal nicotinic receptor control. In the future, this work may lead to the development of a biomarker for anxiety or a diagnostic tool for the early detection of individuals with susceptibility to anxiety.

Frontiers in Behavioral NeuroscienceVol. 18
Rutgers, The State University of New Jersey (US), Lehigh University (US), Johnson University (US)
Directorate for Biological Sciences
Good health and well-being
Openalex Percentile: Top 33%
Nicotinic Acetylcholine Receptors Study
0.47
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.