Dynamic endogenous association of neurofilament mRNAs with K-homology domain ribonucleoproteins in developing cerebral cortex
- PMID: 18054780
- DOI: 10.1016/j.brainres.2007.11.012
Dynamic endogenous association of neurofilament mRNAs with K-homology domain ribonucleoproteins in developing cerebral cortex
Abstract
The low, middle, and high molecular mass neurofilament subunit proteins (NF-L, NF-M, and NF-H) co-polymerize to form neurofilaments (NFs). During development, NF subunit expression is highly regulated, and in neurodegenerative disease, aberrant regulation of this expression can lead to the formation of harmful aggregates. NF expression in both development and disease is under significant post-transcriptional control, but the specific ribonucleoproteins (RNPs) involved are only poorly understood. Previously, mass spectrometry on affinity purified proteins from rat brain identified three K-homology (KH) domain RNPs - hnRNP K, hnRNP E1, hnRNP E2 - as being capable of binding NF-M RNA. In the current study, to determine whether these RNPs associate with NF mRNAs endogenously, we performed a co-immunoprecipitation assay on homogenates of postnatal and developing rat cerebral cortex. We found that all three NF mRNAs indeed associated endogenously with these RNPs and that the degree of this association changed during postnatal development, a period when NF expression is under significant post-transcriptional control. The degree of these associations changed independently of the abundance of either the RNPs or the NF messages, indicating that the RNA-protein interactions themselves are directly regulated. This study is consistent with a model whereby these RNPs and NF mRNAs are components of a dynamic post-transcriptional regulatory module that influences the cytoskeletal compositions of neurons.
Similar articles
-
Dynamic regulation of middle neurofilament RNA pools during optic nerve regeneration.Neuroscience. 2008 Apr 22;153(1):144-53. doi: 10.1016/j.neuroscience.2008.02.001. Epub 2008 Feb 13. Neuroscience. 2008. PMID: 18358619
-
Expression changes of neurofilament subunits in the central nervous system of hens treated with tri-ortho-cresyl phosphate (TOCP).Toxicology. 2006 Jun 1;223(1-2):127-35. doi: 10.1016/j.tox.2006.03.008. Epub 2006 Mar 22. Toxicology. 2006. PMID: 16697097
-
Post-transcriptional control of neurofilaments in development and disease.Exp Cell Res. 2007 Jun 10;313(10):2088-97. doi: 10.1016/j.yexcr.2007.02.014. Epub 2007 Feb 27. Exp Cell Res. 2007. PMID: 17428473 Review.
-
hnRNP K post-transcriptionally co-regulates multiple cytoskeletal genes needed for axonogenesis.Development. 2011 Jul;138(14):3079-90. doi: 10.1242/dev.066993. Development. 2011. PMID: 21693523
-
Precision mechanics with multifunctional tools: how hnRNP K and hnRNPs E1/E2 contribute to post-transcriptional control of gene expression in hematopoiesis.Curr Protein Pept Sci. 2012 Jun;13(4):391-400. doi: 10.2174/138920312801619484. Curr Protein Pept Sci. 2012. PMID: 22708489 Review.
Cited by
-
Heterogeneous nuclear ribonucleoprotein K, an RNA-binding protein, is required for optic axon regeneration in Xenopus laevis.J Neurosci. 2012 Mar 7;32(10):3563-74. doi: 10.1523/JNEUROSCI.5197-11.2012. J Neurosci. 2012. PMID: 22399778 Free PMC article.
-
Neurofilament proteins in axonal regeneration and neurodegenerative diseases.Neural Regen Res. 2012 Mar 15;7(8):620-6. doi: 10.3969/j.issn.1673-5374.2012.08.010. Neural Regen Res. 2012. PMID: 25745454 Free PMC article. Review.
-
eIF4G2 balances its own mRNA translation via a PCBP2-based feedback loop.RNA. 2019 Jul;25(7):757-767. doi: 10.1261/rna.065623.118. Epub 2019 Apr 22. RNA. 2019. PMID: 31010886 Free PMC article.
-
Phosphorylation of poly(rC) binding protein 1 (PCBP1) contributes to stabilization of mu opioid receptor (MOR) mRNA via interaction with AU-rich element RNA-binding protein 1 (AUF1) and poly A binding protein (PABP).Gene. 2017 Jan 20;598:113-130. doi: 10.1016/j.gene.2016.11.003. Epub 2016 Nov 9. Gene. 2017. PMID: 27836661 Free PMC article.
-
Neurofilaments in health and Charcot-Marie-Tooth disease.Front Cell Dev Biol. 2023 Dec 18;11:1275155. doi: 10.3389/fcell.2023.1275155. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 38164457 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Miscellaneous