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      H2O2-dependent translocation of TCTP into the nucleus enables its interaction with VDR in human keratinocytes: TCTP as a further module in calcitriol signalling

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          Abstract

          Translationally controlled tumour protein (TCTP) is an evolutionarily highly conserved molecule implicated in many processes related to cell cycle progression, proliferation and growth, to the protection against harmful conditions including apoptosis and to the human allergic response. We are showing here that after application of mild oxidative stress, human TCTP relocates from the cytoplasm to the nuclei of HaCaT keratinocytes where it directly associates with the ligand-binding domain of endogenous vitamin D(3) receptor (VDR) through its helical domain 2 (AA 71-132). Interestingly, the latter harbours a putative nuclear hormone receptor coregulatory LxxLL-like motif which seems to be involved in the interaction. Moreover, we demonstrate that VDR transcriptionally induces the expression of TCTP by binding to a previously unknown VDR response element within the TCTP promotor. Conversely, ectopically overexpressed TCTP downregulates the amount of VDR on both mRNA as well as protein level. These data, to conclude, suggest a kind of feedback regulation between TCTP and VDR to regulate a variety of (Ca(2+) dependent) cellular effects and in this way further underscore the physiological relevance of this novel protein-protein interaction. Copyright 2009 Elsevier Ltd. All rights reserved.

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          Author and article information

          Journal
          The Journal of Steroid Biochemistry and Molecular Biology
          The Journal of Steroid Biochemistry and Molecular Biology
          Elsevier BV
          09600760
          January 2010
          January 2010
          : 118
          : 1-2
          : 29-40
          Article
          10.1016/j.jsbmb.2009.09.015
          19815065
          75364b37-3aca-4b9c-86a5-ab5dd471b059
          © 2010

          https://www.elsevier.com/tdm/userlicense/1.0/

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