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The kinesin KIF1C transports APC-dependent mRNAs to cell protrusions.

Xavier PichonKonstadinos MoissogluEmeline ColenoTianhong WangArthur ImbertMarie-Cécile RobertMarion PeterRacha ChouaibThomas WalterFlorian MuellerKazem ZibaraEdouard BertrandStavroula Mili
Published in: RNA (New York, N.Y.) (2021)
RNA localization and local translation are important for numerous cellular functions. In mammals, a class of mRNAs localize to cytoplasmic protrusions in an APC-dependent manner, with roles during cell migration. Here, we investigated this localization mechanism. We found that the KIF1C motor interacts with APC-dependent mRNAs and is required for their localization. Live cell imaging revealed rapid, active transport of single mRNAs over long distances that requires both microtubules and KIF1C. Two-color imaging directly revealed single mRNAs transported by single KIF1C motors, with the 3'UTR being sufficient to trigger KIF1C-dependent RNA transport and localization. Moreover, KIF1C remained associated with peripheral, multimeric RNA clusters and was required for their formation. These results reveal a widespread RNA transport pathway in mammalian cells, in which the KIF1C motor has a dual role in transporting RNAs and clustering them within cytoplasmic protrusions. Interestingly, KIF1C also transports its own mRNA, suggesting a possible feedback loop acting at the level of mRNA transport.
Keyphrases
  • single cell
  • cell migration
  • high resolution
  • rna seq
  • genome wide analysis
  • nucleic acid
  • binding protein
  • mass spectrometry
  • bone marrow
  • mesenchymal stem cells
  • high speed
  • atomic force microscopy