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Plakophilins 1 and 3 bind to FXR1 and thereby influence the mRNA stability of desmosomal proteins.
- Source :
-
Molecular and cellular biology [Mol Cell Biol] 2014 Dec 01; Vol. 34 (23), pp. 4244-56. Date of Electronic Publication: 2014 Sep 15. - Publication Year :
- 2014
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Abstract
- Plakophilins 1 and 3 (PKP1/3) are members of the arm repeat family of catenin proteins and serve as structural components of desmosomes, which are important for cell-cell-adhesion. In addition, PKP1/3 occur as soluble proteins outside desmosomes, yet their role in the cytoplasm is not known. We found that cytoplasmic PKP1/3 coprecipitated with the RNA-binding proteins FXR1, G3BP, PABPC1, and UPF1, and these PKP1/3 complexes also comprised desmoplakin and PKP2 mRNAs. Moreover, we showed that the interaction of PKP1/3 with G3BP, PABPC1, and UPF1 but not with FXR1 was RNase sensitive. To address the cytoplasmic function of PKP1/3, we performed gain-and-loss-of-function studies. Both PKP1 and PKP3 knockdown cell lines showed reduced protein and mRNA levels for desmoplakin and PKP2. Whereas global rates of translation were unaffected, desmoplakin and PKP2 mRNA were destabilized. Furthermore, binding of PKP1/3 to FXR1 was RNA independent, and both PKP3 and FXR1 stabilized PKP2 mRNA. Our results demonstrate that cytoplasmic PKP1/3 are components of mRNA ribonucleoprotein particles and act as posttranscriptional regulators of gene expression.<br /> (Copyright © 2014, American Society for Microbiology. All Rights Reserved.)
- Subjects :
- Carrier Proteins metabolism
Cell Adhesion genetics
Cell Line
DNA Helicases
Desmoplakins genetics
Gene Knockdown Techniques
Humans
Plakophilins genetics
Poly(A)-Binding Proteins metabolism
Poly-ADP-Ribose Binding Proteins
Protein Binding
RNA Helicases
RNA Recognition Motif Proteins
RNA, Messenger genetics
RNA-Binding Proteins genetics
Trans-Activators metabolism
Desmosomes genetics
Plakophilins metabolism
RNA Stability genetics
RNA-Binding Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1098-5549
- Volume :
- 34
- Issue :
- 23
- Database :
- MEDLINE
- Journal :
- Molecular and cellular biology
- Publication Type :
- Academic Journal
- Accession number :
- 25225333
- Full Text :
- https://doi.org/10.1128/MCB.00766-14