An N-terminal region of translationally controlled tumor protein is required for its antiapoptotic activity.
Bcl-xL plays a critical role in maintaining cell survival. However, the relationship between the potential interaction of Bcl-xL with other cytosolic proteins and the regulation of cell survival remains incompletely defined. We have identified translationally controlled tumor protein (TCTP), a multifunctional protein, as a novel antiapoptotic Bcl-xL-interacting protein. TCTP interacted ... in vivo and in vitro with Bcl-xL, and their sites have been mapped to an N-terminal region of TCTP and the Bcl-2 homology domain 3 of Bcl-xL. Consistent with a role in maintaining T-cell survival during activation, TCTP was significantly upregulated in murine T cells activated by T-cell antigen receptor (TCR) ligation and CD28 costimulation, which was correlated with the upregulation of Bcl-xL in activated T cells. Moreover, downregulation of TCTP expression by antisense technology in T cells results in the increase of T-cell apoptosis. Furthermore, the N-terminal region of TCTP was required for its ability to inhibit apoptosis. In conclusion, this study has demonstrated that an N-terminal region of a cytosolic protein, TCTP, is required for its binding to Bcl-xL and for its antiapoptotic activity.
Mesh Terms:
Amino Acid Sequence, Animals, Apoptosis, Binding Sites, Humans, Lymphocyte Activation, Mice, Protein Binding, Protein Biosynthesis, Protein Structure, Tertiary, Proteins, Proto-Oncogene Proteins c-bcl-2, Sequence Alignment, T-Lymphocytes, Tumor Markers, Biological, Up-Regulation, bcl-X Protein
Amino Acid Sequence, Animals, Apoptosis, Binding Sites, Humans, Lymphocyte Activation, Mice, Protein Binding, Protein Biosynthesis, Protein Structure, Tertiary, Proteins, Proto-Oncogene Proteins c-bcl-2, Sequence Alignment, T-Lymphocytes, Tumor Markers, Biological, Up-Regulation, bcl-X Protein
Oncogene
Date: Jul. 14, 2005
PubMed ID: 15870695
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