Title: The selective BH4-domain biology of Bcl-2-family members: IP(3)Rs and beyond
Authors: Monaco, Giovanni *
Vervliet, Tim *
Akl, Haidar *
Bultynck, Geert # ×
Issue Date: Apr-2013
Publisher: Birkhäuser Verlag
Series Title: Cellular and Molecular Life Sciences vol:70 issue:7 pages:1171-1183
Abstract: Anti-apoptotic Bcl-2-family members not only neutralize pro-apoptotic proteins but also directly regulate intracellular Ca(2+) signaling from the endoplasmic reticulum (ER), critically controlling cellular health, survival, and death initiation. Furthermore, distinct Bcl-2-family members may selectively regulate inositol 1,4,5-trisphosphate receptor (IP(3)R): Bcl-2 likely acts as an endogenous inhibitor of the IP(3)R, preventing pro-apoptotic Ca(2+) transients, while Bcl-X(L) likely acts as an endogenous IP(3)R-sensitizing protein promoting pro-survival Ca(2+) oscillations. Furthermore, distinct functional domains in Bcl-2 and Bcl-X(L) may underlie the divergence in IP(3)R regulation. The Bcl-2 homology (BH) 4 domain, which targets the central modulatory domain of the IP(3)R, is likely to be Bcl-2's determining factor. In contrast, the hydrophobic cleft targets the C-terminal Ca(2+)-channel tail and might be more crucial for Bcl-X(L)'s function. Furthermore, one amino acid critically different in the sequence of Bcl-2's and Bcl-X(L)'s BH4 domains underpins their selective effect on Ca(2+) signaling and distinct biological properties of Bcl-2 versus Bcl-X(L). This difference is evolutionary conserved across five classes of vertebrates and may represent a fundamental divergence in their biological function. Moreover, these insights open novel avenues to selectively suppress malignant Bcl-2 function in cancer cells by targeting its BH4 domain, while maintaining essential Bcl-X(L) functions in normal cells. Thus, IP(3)R-derived molecules that mimic the BH4 domain's binding site on the IP(3)R may function synergistically with BH3-mimetic molecules selectivity suppressing Bcl-2's proto-oncogenic activity. Finally, a more general role for the BH4 domain on IP(3)Rs, rather than solely anti-apoptotic, may not be excluded as part of a complex network of molecular interactions.
ISSN: 1420-682X
Publication status: published
KU Leuven publication type: IT
Appears in Collections:Laboratory of Molecular and Cellular Signaling
* (joint) first author
× corresponding author
# (joint) last author

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