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NMR assignments of SPOC domain of the human transcriptional corepressor SHARP in complex with a C-terminal SMRT peptide

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Abstract

The transcriptional corepressor SMRT/HDAC1-associated repressor protein (SHARP) recruits histone deacetylases. Human SHARP protein is thought to function in processes involving steroid hormone responses and the Notch signaling pathway. SHARP consists of RNA recognition motifs (RRMs) in the N-terminal region and the spen paralog and ortholog C-terminal (SPOC) domain in the C-terminal region. It is known that the SPOC domain binds the LSD motif in the C-terminal tail of corepressors silencing mediator for retinoid and thyroid receptor (SMRT)/nuclear receptor corepressor (NcoR). We are interested in delineating the mechanism by which the SPOC domain recognizes the LSD motif of the C-terminal tail of SMRT/NcoR. To this end, we are investigating the tertiary structure of the SPOC/SMRT peptide using NMR. Herein, we report on the 1H, 13C and 15N resonance assignments of the SPOC domain in complex with a SMRT peptide, which contributes towards a structural understanding of the SPOC/SMRT peptide and its molecular recognition.

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References

  • Archer SJ, Ikura M, Torchia DA, Bax A (1991) An alternative 3D NMR technique for correlating backbone 15N with side-chain Hβ resonances in larger proteins. J Magn Reson 95:636–641

    Google Scholar 

  • Ariyoshi M, Schwabe JW (2003) A conserved structural motif reveals the essential transcriptional repression function of spen proteins and their role in developmental signaling. Genes Dev 17(15):1909–1920

    Article  Google Scholar 

  • Clowes RT, Boucher W, Hardman CH, Domaille PJ, Laue ED (1993) A 4D HCC(CO)NNH experiment for the correlation of aliphatic side-chain and backbone resonances in 13C/15N-labelled proteins. J Biomol NMR 3:349–354

    Article  Google Scholar 

  • Delaglio F, Grzesiek S, Vuister GW, Zhu G, Pfeifer J, Bax A (1995) NMRPipe: a multidimensional spectral processing system based on UNIX pipes. J Biomol NMR 6(3):277–293

    Article  Google Scholar 

  • Goddard TD, Kneller DG (1999) SPARKY3. University of California, San Francisco

    Google Scholar 

  • Grzesiek S, Ikura M, Clore GM, Gronenborn AM, Bax A (1992) A 3D triple-resonance NMR technique for qualitative measurement of carbonyl-Hβ J couplings in isotopically enriched protein. J Magn Reson 96:215–221

    Google Scholar 

  • Markley JL, Bax A, Arata Y, Hilbers CW, Kaptein R, Sykes BD, Wright PE, Wuthrich K (1998) Recommendations for the presentation of NMR structures of proteins and nucleic acids. IUPAC-IUBMB-IUPAB inter-union task group on the standardization of data bases of protein and nucleic acid structures determined by NMR spectroscopy. J Biomol NMR 12(1):1–23

    Article  Google Scholar 

  • Neri D, Szyperski T, Otting G, Senn H, Wuthrich K (1989) Stereospecific nuclear magnetic resonance assignments of the methyl groups of valine and leucine in the DNA-binding domain of the 434 repressor by biosynthetically directed fractional 13C labeling. Biochemistry 28:7510–7516

    Article  Google Scholar 

  • Oswald F, Kostezka U, Astrahantseff K, Bourteele S, Dillinger K, Zechner U, Ludwig L, Wilda M, Hameister H, Knochel W, Liptay S, Schmid RM (2002) SHARP is a novel component of the Notch/RBP-Jkappa signalling pathway. EMBO J 21(20):5417–5426

    Article  Google Scholar 

  • Sattler M, Schleucher J, Griesinger C (1999) Heteronuclear multidimensional NMR experiments for the structure determination of proteins in solution employing pulsed field gradients. Prog Nucl Magn Reson Spectrosc 34:93–158

    Article  Google Scholar 

  • Shi Y, Downes M, Xie W, Kao HY, Ordentlich P, Tsai CC, Hon M, Evans RM (2001) Sharp, an inducible cofactor that integrates nuclear receptor repression and activation. Genes Dev 15(9):1140–1151

    Article  Google Scholar 

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Acknowledgments

This work was supported in part by a Grant-in-Aid for Scientific Research on Innovative Areas, “Structural Cell Biology” and “Transient Macromolecular Complex” from the Japanese Ministry of Education, Culture, Sports, and Technology (to M.M.), and the Asian Human Resources Fund of Tokyo Metropolitan Government (under Project Asian Network for Major Cities 21) (to Y.I. and M.M.). T.K. is a recipient of a Sasagawa Scientific Research Grant. We thank RIKEN SSBC for help with the 900 MHz NMR measurements.

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Correspondence to Masaki Mishima.

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Mikami, S., Kanaba, T., Ito, Y. et al. NMR assignments of SPOC domain of the human transcriptional corepressor SHARP in complex with a C-terminal SMRT peptide. Biomol NMR Assign 7, 267–270 (2013). https://doi.org/10.1007/s12104-012-9424-8

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  • DOI: https://doi.org/10.1007/s12104-012-9424-8

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