Department of Bio and Brain Engineering, KAIST, Daejeon, Korea.
J Cell Physiol. 2012 Aug;227(8):3027-35. doi: 10.1002/jcp.23044.
Bcl-2/adenovirus E1B 19-kDa interacting protein 1 (BNIP1), which is predominantly localized to the endoplasmic reticulum (ER), is a pro-apoptotic Bcl-2 homology domain 3 (BH3)-only protein. Here, we show that the expression of BNIP1 induced not only a highly interconnected ER network but also mitochondrial fragmentation in a BH3 domain-dependent manner. Functional analysis demonstrated that BNIP1 expression increased dynamin-related protein 1 (Drp1) expression followed by the mitochondrial translocation of Drp1 and subsequent mitochondrial fission. Both BNIP1-induced mitochondrial fission and the translocation of Drp1 were abrogated by Bcl-2 overexpression. These results collectively indicate that ER-specific BNIP1 plays an important role in mitochondrial dynamics by modulating the mitochondrial fission protein Drp1 in a BH3 domain-dependent fashion.
Bcl-2/腺病毒 E1B 19-kDa 相互作用蛋白 1(BNIP1)主要定位于内质网(ER),是一种促凋亡的 Bcl-2 同源结构域 3(BH3)仅蛋白。在这里,我们表明 BNIP1 的表达不仅诱导了高度相互连接的 ER 网络,而且还以 BH3 结构域依赖性方式诱导了线粒体片段化。功能分析表明,BNIP1 的表达增加了与动力相关蛋白 1(Drp1)的表达,随后 Drp1 的线粒体易位和随后的线粒体分裂。Bcl-2 的过表达可以阻断 BNIP1 诱导的线粒体分裂和 Drp1 的易位。这些结果共同表明,ER 特异性 BNIP1 通过以 BH3 结构域依赖性方式调节线粒体分裂蛋白 Drp1 在调节线粒体动力学方面发挥重要作用。