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TCTP contains a BH3-like domain, which instead of inhibiting, activates Bcl-xL.

Authors :
Thébault S
Agez M
Chi X
Stojko J
Cura V
Telerman SB
Maillet L
Gautier F
Billas-Massobrio I
Birck C
Troffer-Charlier N
Karafin T
Honoré J
Senff-Ribeiro A
Montessuit S
Johnson CM
Juin P
Cianférani S
Martinou JC
Andrews DW
Amson R
Telerman A
Cavarelli J
Source :
Scientific reports [Sci Rep] 2016 Jan 27; Vol. 6, pp. 19725. Date of Electronic Publication: 2016 Jan 27.
Publication Year :
2016

Abstract

Translationally Controlled Tumor Protein (TCTP) is anti-apoptotic, key in development and cancer, however without the typical Bcl2 family members' structure. Here we report that TCTP contains a BH3-like domain and forms heterocomplexes with Bcl-xL. The crystal structure of a Bcl-xL deletion variant-TCTP11-31 complex reveals that TCTP refolds in a helical conformation upon binding the BH3-groove of Bcl-xL, although lacking the h1-subregion interaction. Experiments using in vitro-vivo reconstituted systems and TCTP(+/-) mice indicate that TCTP activates the anti-apoptotic function of Bcl-xL, in contrast to all other BH3-proteins. Replacing the non-conserved h1 of TCTP by that of Bax drastically increases the affinity of this hybrid for Bcl-xL, modifying its biological properties. This work reveals a novel class of BH3-proteins potentiating the anti-apoptotic function of Bcl-xL.

Details

Language :
English
ISSN :
2045-2322
Volume :
6
Database :
MEDLINE
Journal :
Scientific reports
Publication Type :
Academic Journal
Accession number :
26813996
Full Text :
https://doi.org/10.1038/srep19725