Protein phosphatase 4 interacts with the Survival of Motor Neurons complex and enhances the temporal localisation of snRNPs
- PMID: 12668731
- DOI: 10.1242/jcs.00409
Protein phosphatase 4 interacts with the Survival of Motor Neurons complex and enhances the temporal localisation of snRNPs
Expression of concern in
-
Expression of Concern: Protein phosphatase 4 interacts with the Survival of Motor Neurons complex and enhances the temporal localisation of snRNPs.J Cell Sci. 2022 Oct 1;135(19):jcs260640. doi: 10.1242/jcs.260640. Epub 2022 Sep 29. J Cell Sci. 2022. PMID: 36173032 No abstract available.
Abstract
Protein phosphatase 4 (PPP4) is a ubiquitous essential protein serine/threonine phosphatase found in higher eukaryotes. Coordinate variation of the levels of the catalytic subunit (PPP4c) and the regulatory subunit (R2) suggests that PPP4c and R2 form a heterodimeric core to which other regulatory subunits bind. Two proteins that specifically co-purify with Flag-epitope-tagged R2 expressed in HEK-293 cells were identified as Gemin3 and Gemin4. These two proteins have been identified previously as components of the Survival of Motor Neurons (SMN) protein complex, which is functionally defective in the hereditary disorder spinal muscular atrophy. Immuno-sedimentation of the epitope-tagged SMN protein complex from HeLa cells expressing CFP-SMN showed that the SMN protein interacts, as previously reported, with Gemin2 (SIP1), Gemin3 and Gemin4 and in addition associates with PPP4c. The SMN complex has been implicated in the assembly and maturation of small nuclear ribonucleoproteins (snRNPs). Expression of GFP-R2-PPP4c in HeLa cells enhances the temporal localisation of newly formed snRNPs, which is consistent with an association of R2-PPP4c with the SMN protein complex.
Similar articles
-
Gemin proteins are required for efficient assembly of Sm-class ribonucleoproteins.Proc Natl Acad Sci U S A. 2005 Nov 29;102(48):17372-7. doi: 10.1073/pnas.0508947102. Epub 2005 Nov 21. Proc Natl Acad Sci U S A. 2005. PMID: 16301532 Free PMC article.
-
Gemin5, a novel WD repeat protein component of the SMN complex that binds Sm proteins.J Biol Chem. 2002 Feb 15;277(7):5631-6. doi: 10.1074/jbc.M109448200. Epub 2001 Nov 19. J Biol Chem. 2002. PMID: 11714716
-
Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems.J Cell Biol. 1999 Dec 13;147(6):1181-94. doi: 10.1083/jcb.147.6.1181. J Cell Biol. 1999. PMID: 10601333 Free PMC article.
-
Macromolecular complexes: SMN--the master assembler.Curr Biol. 2001 Oct 30;11(21):R862-4. doi: 10.1016/s0960-9822(01)00517-6. Curr Biol. 2001. PMID: 11696342 Review.
-
The SMN complex.Exp Cell Res. 2004 May 15;296(1):51-6. doi: 10.1016/j.yexcr.2004.03.022. Exp Cell Res. 2004. PMID: 15120993 Review.
Cited by
-
Presynaptic localization of Smn and hnRNP R in axon terminals of embryonic and postnatal mouse motoneurons.PLoS One. 2014 Oct 22;9(10):e110846. doi: 10.1371/journal.pone.0110846. eCollection 2014. PLoS One. 2014. PMID: 25338097 Free PMC article.
-
UsnRNP biogenesis: mechanisms and regulation.Chromosoma. 2017 Oct;126(5):577-593. doi: 10.1007/s00412-017-0637-6. Epub 2017 Aug 1. Chromosoma. 2017. PMID: 28766049 Review.
-
A PP4-phosphatase complex dephosphorylates gamma-H2AX generated during DNA replication.Mol Cell. 2008 Jul 11;31(1):33-46. doi: 10.1016/j.molcel.2008.05.016. Mol Cell. 2008. PMID: 18614045 Free PMC article.
-
SMN post-translational modifications in spinal muscular atrophy.Front Cell Neurosci. 2023 Feb 17;17:1092488. doi: 10.3389/fncel.2023.1092488. eCollection 2023. Front Cell Neurosci. 2023. PMID: 36874214 Free PMC article. Review.
-
Gigaxonin, mutated in Giant Axonal Neuropathy, interacts with TDP-43 and other RNA binding proteins.bioRxiv [Preprint]. 2024 Sep 5:2024.09.03.611033. doi: 10.1101/2024.09.03.611033. bioRxiv. 2024. PMID: 39282431 Free PMC article. Preprint.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Research Materials
Miscellaneous