We have been able to observe the dynamic interactions between a specific messenger RNA (mRNA) and its protein product in vivo by studying the synthesis and assembly of peripherin intermediate filaments (IFs). The results show that peripherin mRNA-containing particles (messenger ribonucleoproteins [mRNPs]) move mainly along microtubules (MT). These mRNPs are translationally silent, initiating translation when they cease moving. Many peripherin mRNPs contain multiple mRNAs, possibly amplifying the total amount of protein synthesized within these “translation factories.” This mRNA clustering is dependent on MT, regulatory sequences within the RNA and the nascent protein. Peripherin is cotranslationally assembled into insoluble, nonfilamentous particles that are precursors to the long IF that form extensive cytoskeletal networks. The results show that the motility and targeting of peripherin mRNPs, their translational control, and the assembly of an IF cytoskeletal system are linked together in a process we have termed dynamic cotranslation.
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27 February 2006
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February 27 2006
Assembling an intermediate filament network by dynamic cotranslation
Lynne Chang,
Lynne Chang
1Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611
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Yaron Shav-Tal,
Yaron Shav-Tal
2Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan 52900, Israel
3Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY 10461
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Tatjana Trcek,
Tatjana Trcek
3Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY 10461
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Robert H. Singer,
Robert H. Singer
3Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY 10461
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Robert D. Goldman
Robert D. Goldman
1Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611
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Lynne Chang
1Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611
Yaron Shav-Tal
2Faculty of Life Sciences, Bar-Ilan University, Ramat-Gan 52900, Israel
3Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY 10461
Tatjana Trcek
3Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY 10461
Robert H. Singer
3Department of Anatomy and Structural Biology, Albert Einstein College of Medicine, Bronx, NY 10461
Robert D. Goldman
1Department of Cell and Molecular Biology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611
Correspondence to Lynne Chang: [email protected]
Abbreviations used in this paper: 3D, three-dimensional; CDS, coding sequence; DM, differentiation medium; ECFP, enhanced CFP; IF, intermediate filament; mRNP, messenger RNP; MT, microtubules; TFI, total fluorescent intensity; ULF, unit-length filament; UTR, untranslated region.
Received:
November 21 2005
Accepted:
January 23 2006
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2006
J Cell Biol (2006) 172 (5): 747–758.
Article history
Received:
November 21 2005
Accepted:
January 23 2006
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This article has been corrected
Correction: Assembling an intermediate filament network by dynamic cotranslation
Citation
Lynne Chang, Yaron Shav-Tal, Tatjana Trcek, Robert H. Singer, Robert D. Goldman; Assembling an intermediate filament network by dynamic cotranslation . J Cell Biol 27 February 2006; 172 (5): 747–758. doi: https://doi.org/10.1083/jcb.200511033
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