Caria Sofia, Hinds Mark G, Kvansakul Marc
Department of Biochemistry & Genetics, La Trobe Institute for Molecular Science, La Trobe University, Melbourne,Victoria 3086, Australia.
Department of Chemistry & Physics, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, Victoria 3086, Australia.
Cell Death Dis. 2017 Jan 12;8(1):e2543. doi: 10.1038/cddis.2016.469.
Sponges of the porifera family harbor some of the evolutionary most ancient orthologs of the B-cell lymphoma-2 (Bcl-2) family, a protein family critical to regulation of apoptosis. The genome of the sponge Geodia cydonium contains the putative pro-survival Bcl-2 homolog BHP2, which protects sponge tissue as well as mammalian Hek-293 and NIH-3T3 cells against diverse apoptotic stimuli. The Lake Baikal demosponge Lubomirskia baicalensis has been shown to encode both putative pro-survival Bcl-2 (LB-Bcl-2) and pro-apoptotic Bcl-2 members (LB-Bak-2), which have been implied in axis formation (branches) in L. baicalensis. However, the molecular mechanism of action of sponge-encoded orthologs of Bcl-2 remains to be clarified. Here, we report that the pro-survival Bcl-2 ortholog BHP2 from G. cydonium is able to bind the BH3 motif of a pro-apoptotic Bcl-2 protein, LB-Bak-2 of the sponge L. baicalensis. Furthermore, we determined the crystal structure of BHP2 bound to LB-Bak-2, which revealed that using a binding groove conserved across all pro-survival Bcl-2 proteins, BHP2 binds multi-motif Bax-like proteins through their BH3-binding regions. However, BHP2 discriminates against BH3-only bearing proteins by blocking access to a hydrophobic pocket that is critical for BH3 motif binding in pro-survival Bcl-2 proteins from higher organisms. This differential binding mode is reflected in a structure-based phylogenetic comparison of BHP2 with other Bcl-2 family members, which revealed that BHP2 does not cluster with either Bcl-2 members of higher organisms or pathogen-encoded homologs, and assumes a discrete position. Our findings suggest that the molecular machinery and mechanisms for executing Bcl-2-mediated apoptosis as observed in mammals are evolutionary ancient, with early regulation of apoptotic machineries closely resembling their modern counterparts in mammals rather than Caenorhabditis elegans or drosophila.
多孔动物门的海绵含有一些进化上最古老的B细胞淋巴瘤-2(Bcl-2)家族直系同源物,这是一个对细胞凋亡调控至关重要的蛋白质家族。海绵Geodia cydonium的基因组包含假定的促生存Bcl-2同源物BHP2,它能保护海绵组织以及哺乳动物的Hek-293和NIH-3T3细胞免受多种凋亡刺激。贝加尔湖的硬海绵Lubomirskia baicalensis已被证明能编码假定的促生存Bcl-2(LB-Bcl-2)和促凋亡Bcl-2成员(LB-Bak-2),它们与L. baicalensis的轴形成(分支)有关。然而,海绵编码的Bcl-2直系同源物的分子作用机制仍有待阐明。在这里,我们报告来自G. cydonium的促生存Bcl-2直系同源物BHP2能够结合促凋亡Bcl-2蛋白LB-Bak-2的BH3基序,LB-Bak-2来自海绵L. baicalensis。此外,我们确定了与LB-Bak-2结合的BHP2的晶体结构,结果表明,通过一个在所有促生存Bcl-2蛋白中保守的结合凹槽,BHP2通过其BH3结合区域结合多基序Bax样蛋白。然而,BHP2通过阻断进入一个疏水口袋来区分仅含BH3的蛋白,这个疏水口袋对于高等生物促生存Bcl-2蛋白中BH3基序的结合至关重要。这种差异结合模式反映在基于结构的BHP2与其他Bcl-2家族成员的系统发育比较中,结果表明BHP2既不与高等生物的Bcl-2成员聚类,也不与病原体编码的同源物聚类,而是处于一个离散的位置。我们的研究结果表明,哺乳动物中观察到的执行Bcl-2介导的细胞凋亡的分子机制和机器在进化上很古老,凋亡机器的早期调控与其在哺乳动物中的现代对应物非常相似,而不是与秀丽隐杆线虫或果蝇相似。