Knockdown of RNP1A reduces cell proliferation and adhesion in Dictyostelium, suggesting its role in regulating cell mechanics.
Cell shape regulation is important for many biological processes. Some cell shape-regulating proteins harbor mechanoresponsive properties that enable them to sense and respond to mechanical cues. In Dictyostelium discoideum, mechanoresponsive network proteins like Myosin II, Cortexillin I and IQGAP1 assemble in the cytoplasm into macromolecular complexes, which we term Contractility Kits. In our previous studies, we identified the RNA-binding protein, RNP1A, as a genetic interactor with the cell's cytoskeletal machinery and as a biochemical interactor of Cortexillin I, using in vivo fluorescence cross-correlation spectroscopy. In this study, the rnp1A knockdown cells have reduced cell proliferation, reduced adhesion, defective cytokinesis, and a gene expression profile that indicates rnp1A knockdown cells shift away from the vegetative growth state. RNP1A binds transcripts some of which encode proteins involved in macropinocytosis, a critical cell shape change process. Loss of other CK proteins leads to macropinocytotic defects characterized by reduced macropinocytotic crown size. RNP1A interacts with IQGAP1, leading to crosstalk during macropinocytosis. Overall, RNP1A binds transcripts and contributes to cell mechanics and cell shape change processes through interactions with Contractility Kit proteins.
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Ly T.S. Nguyen (2025) studied this question.
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