Biology:CUGBP1

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CUG triplet repeat, RNA binding protein 1, also known as CUGBP1, is a protein which in humans is encoded by the CUGBP1 gene.[1][2][3]

Function

Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing, and translation. This gene may play a role in myotonic dystrophy type 1 (DM1) via interactions with the dystrophia myotonica-protein kinase (DMPK) gene. Alternative splicing results in multiple transcript variants encoding different isoforms.[1]

mRNA degradation factor

It is estimated that 5 to 8% of human mRNAs are unstable because of mRNA instability elements in their 3' untranslated regions (3'UTR).[4] A number of such elements have been called AU-rich elements (AREs). It is now known that AREs are binding sites for RNA-binding proteins that target mRNAs to rapid degradation. However, only few of the proteins reported to bind AREs were demonstrated to play a role in mRNA degradation. A shared feature of these proteins is to bind only to a subclass of the known AREs that contain the pentamer AUUUA. A convergent effort of several research teams now adds CUGBP1 (CUG binding protein 1) to the short list of ARE-Binding proteins that control mRNA stability, with the peculiarity that it binds to non-AUUUA AREs. CUGBP1 has been involved both as a key regulator of human myotonic dystrophy 1 (DM1) and more recently as a regulator of human papilloma virus mRNA expression.[5]

Evidence for CUGBP1 acting as a RNA degradation factor came first from the Xenopus model. Xenopus CUGBP1 (xCUGBP1, formerly known as EDEN-BP) was identified in 1998[6] for its ability to bind specifically to a GU-rich element (Embryonic deadenylation element EDEN) located in the 3'UTRs of some mRNAs that are rapidly deadenylated and translationally repressed after fertilization in early development. Because deadenylation is often the rate limiting step of mRNA degradation the enhancement of deadenylation increases mRNA turnover.[7]

Human CUGBP1 (hCUGBP1) had been previously identified by Timchenko and colleagues[2] for its ability to bind to CUG repeats located in the DMPK 3'UTR. A large amount of work has since described the role of hCUGBP1 on control of alternative splicing and will not be discussed here.[8] The demonstration that hCUGBP1 is involved in the control of mRNA deadenylation and instability like xCUGBP1 came next. In mammalian cell extract as well as in xenopus egg extracts, depletion and rescue experiments showed that specific binding of CUGBP1 to the 3'UTR of mRNA is required for the targeted specific deadenylation to occur.[9] In rescue experiments in xenopus egg extracts, the recombinant human protein can replace the xenopus one making them functional homolog.[10] Furthermore, the Poly(A) ribonuclease PARN was shown to interact with CUGBP1.[11] In human cells, tethering of hCUGBP1 to a mRNA decreases its steadystate suggesting the destabilization of the mRNA.[12] The first human mRNA reported to be targeted to rapid deadenylation and degradation by CUGBP1 is the oncogene c-jun. Years ago, it was shown that the class III ARE (devoid of any AUUUA motif) of the human c-jun oncogene directed rapid deadenylation and degradation to a reporter mRNA.[13] Both xCUGBP1 and hCUGBP1 were shown to specifically bind to c-jun ARE.[9] The binding of CUGBP1 to the 3'UTR of mRNAs bearing GU-rich element would target these mRNAs for rapid deadenylation by PARN and subsequent degradation. This was recently demonstrated by siRNA-mediated knockdown of hCUGBP1 that led to stabilization of a reporter RNA bearing the c-jun UG -rich ARE.[14]

UGU(G/A) tetranucleotides are key determinants of the binding site for xCUGBP1. A SELEX approach for the identification of artificial substrate of hCUGBP1 led to the proposition that UGU containing sequences were highly favoured for binding.[15] More recently, the reappraisal of CUGBP1 binding sites on the base of a combination of the SELEX approach and

Immunoprecipitation of the CUGBP1 containing complexes has led Graindorge et al. to propose a 15 nt motif as a key determinant of CUGBP1 binding.[16] Such a motif is found in a number of unstable mRNAs in human cells[14] suggesting that they are degraded by a CUGBP1 deadenylation dependent pathway.

References

  1. ↑ 1.0 1.1 "Entrez Gene: CUGBP1 CUG triplet repeat, RNA binding protein 1". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10658. 
  2. ↑ 2.0 2.1 "Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophy". Nucleic Acids Res. 24 (22): 4407–14. November 1996. doi:10.1093/nar/24.22.4407. PMID 8948631. 
  3. ↑ "Altered phosphorylation and intracellular distribution of a (CUG)n triplet repeat RNA-binding protein in patients with myotonic dystrophy and in myotonin protein kinase knockout mice". Proc. Natl. Acad. Sci. U.S.A. 94 (24): 13221–6. November 1997. doi:10.1073/pnas.94.24.13221. PMID 9371827. Bibcode: 1997PNAS...9413221R. 
  4. ↑ "ARED: human AU-rich element-containing mRNA database reveals an unexpectedly diverse functional repertoire of encoded proteins". Nucleic Acids Res. 29 (1): 246–54. January 2001. doi:10.1093/nar/29.1.246. PMID 11125104. 
  5. ↑ "The regulatory element in the 3'-untranslated region of human papillomavirus 16 inhibits expression by binding CUG-binding protein 1". J. Biol. Chem. 283 (4): 2286–96. January 2008. doi:10.1074/jbc.M708789200. PMID 18042543. 
  6. ↑ "EDEN and EDEN-BP, a cis element and an associated factor that mediate sequence-specific mRNA deadenylation in Xenopus embryos". EMBO J. 17 (1): 278–87. January 1998. doi:10.1093/emboj/17.1.278. PMID 9427761. 
  7. ↑ "Messenger RNA turnover in eukaryotes: pathways and enzymes". Crit. Rev. Biochem. Mol. Biol. 39 (4): 197–216. 2004. doi:10.1080/10409230490513991. PMID 15596551. 
  8. ↑ "Elevation of RNA-binding protein CUGBP1 is an early event in an inducible heart-specific mouse model of myotonic dystrophy". J. Clin. Invest. 117 (10): 2802–11. October 2007. doi:10.1172/JCI32308. PMID 17823658. 
  9. ↑ 9.0 9.1 "c-Jun ARE targets mRNA deadenylation by an EDEN-BP (embryo deadenylation element-binding protein)-dependent pathway". J. Biol. Chem. 277 (5): 3232–5. February 2002. doi:10.1074/jbc.M109362200. PMID 11707455. 
  10. ↑ "A functional deadenylation assay identifies human CUG-BP as a deadenylation factor". Biol. Cell 95 (2): 107–13. 2003. doi:10.1016/S0248-4900(03)00010-8. PMID 12799066. 
  11. ↑ "CUG-BP binds to RNA substrates and recruits PARN deadenylase". RNA 12 (6): 1084–91. June 2006. doi:10.1261/rna.59606. PMID 16601207. 
  12. ↑ "Protein expression is increased by a class III AU-rich element and tethered CUG-BP1". Biochem. Biophys. Res. Commun. 347 (3): 723–30. September 2006. doi:10.1016/j.bbrc.2006.06.177. PMID 16843434. 
  13. ↑ "Functional characterization of a non-AUUUA AU-rich element from the c-jun proto-oncogene mRNA: evidence for a novel class of AU-rich elements". Mol. Cell. Biol. 16 (4): 1490–9. April 1996. doi:10.1128/MCB.16.4.1490. PMID 8657122. 
  14. ↑ 14.0 14.1 "Conserved GU-Rich Elements Mediate mRNA Decay by Binding to CUG-Binding Protein 1". Mol. Cell 29 (2): 263–70. February 2008. doi:10.1016/j.molcel.2007.11.024. PMID 18243120. 
  15. ↑ "CUG-BP1/CELF1 requires UGU-rich sequences for high-affinity binding". Biochem. J. 400 (2): 291–301. December 2006. doi:10.1042/BJ20060490. PMID 16938098. 
  16. ↑ "Identification of CUG-BP1/EDEN-BP target mRNAs in Xenopus tropicalis". Nucleic Acids Res. 36 (6): 1861–70. April 2008. doi:10.1093/nar/gkn031. PMID 18267972. 

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