The Impact of Zyxin Modifications on Its Intracellular Distribution in the Xenopus Laevis Embryo Model

Objective: The aim of this study is to investigate the mechanisms underlying the intracellular transport of the mechanosensitive protein zyxin. Zyxin, a conserved LIM domain protein, plays a critical role in regulating the assembly of F-actin filaments at cellular junctions. In response to mechanical stimuli such as cell stretch, zyxin has the capacity to translocate into the nucleus to influence gene expression, or it may exit the nucleus. Importantly, zyxin is recognized as a tumor marker, making the exploration of its post-translational modifications and the dynamics of its nuclear-cytoplasmic shuttling significant for advancements in molecular diagnostics related to disease. Methods: To elucidate the nuclear entry dynamics of zyxin, we employed site-directed mutagenesis to selectively target palmitylation sites, O-GlcNAcylation sites, and specific amino acids at both the N- and C-termini. This investigation was conducted using Xenopus laevis gastrula embryos, which serve as an effective model for studying protein trafficking. Results and Discussion: Our findings reveal that the introduction of a Flag epitope at the C-terminus of the zyxin molecule results in a loss of its nuclear translocation capability. Conversely, mutating the palmitylation sites leads to a noticeable decrease in the nuclear presence of zyxin, while modifications to amino acids responsible for O-GlcNAcylation result in an increased accumulation of zyxin in the nucleus. Conclusions: The data obtained from this study highlight the significant impact of these specific post-translational modifications on the subcellular localization of zyxin. These findings contribute to the broader research knowledge regarding the mechanistic aspects of the localization dynamics of zyxin and related mechanosensitive proteins. Given that the disruption of intracellular localization can have profound implications in the development of cancer and cardiovascular diseases, this research bears both fundamental and medical importance.

Authors

Institutions

Publication Details

Journal
Russian Journal of Bioorganic Chemistry
Published
2025-04-01
DOI
https://doi.org/10.1134/s1068162024605755
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

The Impact of Zyxin Modifications on Its Intracellular Distribution in the Xenopus Laevis Embryo Model

N. Y. Martynova, Andrey G. Zaraisky, Е. А. Паршина, E. D. Ivanova
Russian Journal of Bioorganic Chemistry
Cellular Mechanics and Interactions
article

The Impact of Zyxin Modifications on Its Intracellular Distribution in the Xenopus Laevis Embryo Model

N. Y. Martynova, Andrey G. Zaraisky, Е. А. Паршина, E. D. Ivanova
article en

Abstract

Objective: The aim of this study is to investigate the mechanisms underlying the intracellular transport of the mechanosensitive protein zyxin. Zyxin, a conserved LIM domain protein, plays a critical role in regulating the assembly of F-actin filaments at cellular junctions. In response to mechanical stimuli such as cell stretch, zyxin has the capacity to translocate into the nucleus to influence gene expression, or it may exit the nucleus. Importantly, zyxin is recognized as a tumor marker, making the exploration of its post-translational modifications and the dynamics of its nuclear-cytoplasmic shuttling significant for advancements in molecular diagnostics related to disease. Methods: To elucidate the nuclear entry dynamics of zyxin, we employed site-directed mutagenesis to selectively target palmitylation sites, O-GlcNAcylation sites, and specific amino acids at both the N- and C-termini. This investigation was conducted using Xenopus laevis gastrula embryos, which serve as an effective model for studying protein trafficking. Results and Discussion: Our findings reveal that the introduction of a Flag epitope at the C-terminus of the zyxin molecule results in a loss of its nuclear translocation capability. Conversely, mutating the palmitylation sites leads to a noticeable decrease in the nuclear presence of zyxin, while modifications to amino acids responsible for O-GlcNAcylation result in an increased accumulation of zyxin in the nucleus. Conclusions: The data obtained from this study highlight the significant impact of these specific post-translational modifications on the subcellular localization of zyxin. These findings contribute to the broader research knowledge regarding the mechanistic aspects of the localization dynamics of zyxin and related mechanosensitive proteins. Given that the disruption of intracellular localization can have profound implications in the development of cancer and cardiovascular diseases, this research bears both fundamental and medical importance.

Russian Journal of Bioorganic ChemistryVol. 51(2)
Pirogov Russian National Research Medical University (RU), Institute of Bioorganic Chemistry (RU)
Zero hunger, Life in Land
Openalex Percentile: Top 92%
Cellular Mechanics and Interactions
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.