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LINKIN-associated proteins necessary for tissue integrity during collective cell migration. | LitMetric

AI Article Synopsis

  • Cell adhesion is crucial for various biological processes, and LINKIN (ITFG1) is a transmembrane protein essential for maintaining tissue integrity during cell migration.
  • Loss of LINKIN leads to cell detachment in the developing male gonad, and its interaction with proteins like RUVBL1 and alpha-tubulin has implications in processes like metastasis in breast cancer.
  • New potential interactors of LINKIN were discovered through analysis, indicating that membrane remodeling and chromosome biology may play important roles in its function related to cell adhesion.

Article Abstract

Cell adhesion plays essential roles in almost every aspect of metazoan biology. LINKIN (Human: ITFG1, : ) is a conserved transmembrane protein that has been identified to be necessary for tissue integrity during migration. In , loss of results in the detachment of the lead migratory cell from the rest of the developing male gonad. Previously, three interactors of ITFG1/ - RUVBL1/, RUVBL2/, and alpha-tubulin - were identified by immunoprecipitation-mass spectrometry (IP-MS) analysis using human HEK293T cells and then validated in the nematode male gonad. The ITFG1-RUVBL1 interaction has since been independently validated in a breast cancer cell line model that also implicates the involvement of the pair in metastasis. Here, we showed that epitope-tagged ITFG1 localized to the cell surface of MDA-MB-231 breast cancer cells. Using IP-MS analysis, we identified a new list of potential interactors of ITFG1. analysis of their orthologs found that three of the interactors - ATP9A/, NME1/, and ANAPC2/ - displayed migratory detachment phenotypes similar to that of . Taken together with the other genes whose reduction-of-function phenotype is similar to that of (notably cohesion and condensin), suggests the involvement of membrane remodeling and chromosome biology in LINKIN-dependent cell adhesion and supports the hypothesis for a structural role of chromosomes in post-mitotic cells.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934607PMC
http://dx.doi.org/10.1101/2023.02.08.527750DOI Listing

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