Biology:Exosome component 3
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Exosome component 3, also known as EXOSC3, is a human gene, which is part of the exosome complex.[1]
Clinical significance
Mutations in EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration.[2]
References
- ↑ "Entrez Gene: EXOSC3 exosome component 3". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=51010.
- ↑ "Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration". Nat. Genet. 44 (6): 704–8. 2012. doi:10.1038/ng.2254. PMID 22544365.
Further reading
- "The yeast exosome and human PM-Scl are related complexes of 3' --> 5' exonucleases.". Genes Dev. 13 (16): 2148–58. 1999. doi:10.1101/gad.13.16.2148. PMID 10465791.
- "Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics.". Genome Res. 10 (5): 703–13. 2000. doi:10.1101/gr.10.5.703. PMID 10810093.
- "Three novel components of the human exosome.". J. Biol. Chem. 276 (9): 6177–84. 2001. doi:10.1074/jbc.M007603200. PMID 11110791.
- "AU binding proteins recruit the exosome to degrade ARE-containing mRNAs.". Cell 107 (4): 451–64. 2002. doi:10.1016/S0092-8674(01)00578-5. PMID 11719186.
- "Directed proteomic analysis of the human nucleolus.". Curr. Biol. 12 (1): 1–11. 2002. doi:10.1016/S0960-9822(01)00650-9. PMID 11790298.
- "Protein-protein interactions of hCsl4p with other human exosome subunits.". J. Mol. Biol. 315 (4): 809–18. 2002. doi:10.1006/jmbi.2001.5265. PMID 11812149.
- "Autoantibodies directed to novel components of the PM/Scl complex, the human exosome.". Arthritis Res. 4 (2): 134–8. 2002. doi:10.1186/ar389. PMID 11879549.
- "Protein-protein interactions between human exosome components support the assembly of RNase PH-type subunits into a six-membered PNPase-like ring.". J. Mol. Biol. 323 (4): 653–63. 2002. doi:10.1016/S0022-2836(02)00947-6. PMID 12419256.
- "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. 2003. doi:10.1073/pnas.242603899. PMID 12477932.
- "A KH domain RNA binding protein, KSRP, promotes ARE-directed mRNA turnover by recruiting the degradation machinery.". Mol. Cell 14 (5): 571–83. 2004. doi:10.1016/j.molcel.2004.05.002. PMID 15175153.
- "A protein interaction framework for human mRNA degradation.". Genome Res. 14 (7): 1315–23. 2004. doi:10.1101/gr.2122004. PMID 15231747.
- "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. 2004. doi:10.1101/gr.2596504. PMID 15489334.
- "Towards a proteome-scale map of the human protein-protein interaction network.". Nature 437 (7062): 1173–8. 2005. doi:10.1038/nature04209. PMID 16189514.
External links
- Overview of all the structural information available in the PDB for UniProt: Q9NQT5 (Human Exosome complex component RRP40) at the PDBe-KB.