A KIF1C-CNBP motor-adaptor complex for trafficking mRNAs to cell protrusions

mRNA localization to subcellular compartments is a widely used mechanism that functionally contributes to numerous processes. mRNA targeting can be achieved upon recognition of RNA cargo by molecular motors. However, our molecular understanding of how this is accomplished is limited, especially in higher organisms. We focus on a pathway that targets mRNAs to peripheral protrusions of mammalian cells and which is important for cell migration. Trafficking occurs through active transport on microtubules, mediated by the KIF1C kinesin. Here, we identify the RNA-binding protein CNBP as a factor required for mRNA localization to protrusions. CNBP binds directly to GA-rich sequences in the 3' UTR of protrusion-targeted mRNAs. CNBP also interacts with KIF1C and is required for KIF1C recruitment to mRNAs and their trafficking on microtubules to the periphery. This work provides a molecular mechanism for KIF1C recruitment to mRNA cargo and reveals a motor-adaptor complex for mRNA transport to cell protrusions.

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Publication Details

Journal
Cell Reports
Published
2025-02-20
DOI
https://doi.org/10.1016/j.celrep.2025.115346
Citations
4
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
3.22

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article

A KIF1C-CNBP motor-adaptor complex for trafficking mRNAs to cell protrusions

Lisa M. Miller Jenkins, Alexander N. Gasparski, Konstadinos Moissoglu, Elliott L. Paine et al.
4 citations
Cell Reports
RNA Research and Splicing
3.22
article

A KIF1C-CNBP motor-adaptor complex for trafficking mRNAs to cell protrusions

Lisa M. Miller Jenkins, Alexander N. Gasparski, Konstadinos Moissoglu, Elliott L. Paine, Tianhong Wang, Michael Stueland, Stavroula Mili
article en
4 citations

Abstract

mRNA localization to subcellular compartments is a widely used mechanism that functionally contributes to numerous processes. mRNA targeting can be achieved upon recognition of RNA cargo by molecular motors. However, our molecular understanding of how this is accomplished is limited, especially in higher organisms. We focus on a pathway that targets mRNAs to peripheral protrusions of mammalian cells and which is important for cell migration. Trafficking occurs through active transport on microtubules, mediated by the KIF1C kinesin. Here, we identify the RNA-binding protein CNBP as a factor required for mRNA localization to protrusions. CNBP binds directly to GA-rich sequences in the 3' UTR of protrusion-targeted mRNAs. CNBP also interacts with KIF1C and is required for KIF1C recruitment to mRNAs and their trafficking on microtubules to the periphery. This work provides a molecular mechanism for KIF1C recruitment to mRNA cargo and reveals a motor-adaptor complex for mRNA transport to cell protrusions.

Cell ReportsVol. 44(3)
National Cancer Institute (US), Center for Cancer Research (US)
National Cancer Institute
Gender equality
Openalex Percentile: Top 9%
RNA Research and Splicing
3.22
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A KIF1C-CNBP motor-adaptor complex for trafficking mRNAs to cell protrusions — Lisa M. Miller Jenkins, Alexander N. Gasparski, et al. · Cell Reports (2025) | TGRS Research Map | TGRS