Katoh Keiichi, Suzuki Hidenori, Terasawa Yoshinori, Mizuno Takako, Yasuda Jiro, Shibata Hideki, Maki Masatoshi
Department of Applied Molecular Biosciences, Graduate School of Bioagricultural Sciences, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8601, Japan.
Biochem J. 2005 Nov 1;391(Pt 3):677-85. doi: 10.1042/BJ20050398.
ALG-2 (apoptosis-linked gene 2) is a Ca2+-binding protein that belongs to the PEF (penta-EF-hand) protein family. Alix (ALG-2-interacting protein X)/AIP1 (ALG-2-interacting protein 1), one of its binding partners, interacts with TSG101 and CHMP4 (charged multivesicular body protein 4), which are components of ESCRT-I (endosomal sorting complex required for transport I) and ESCRT-III respectively. In the present study, we investigated the association between ALG-2 and ESCRT-I. By a GST (glutathione S-transferase) pull-down assay using HEK-293T (human embryonic kidney 293T) cell lysates, endogenous TSG101 and two other exogenously expressed ESCRT-I components [hVps28 (human vacuolar protein sorting 28) and hVps37A] were shown to associate with GST-ALG-2 in the presence of Ca2+. By the yeast two-hybrid assay, however, a positive interaction was observed with only TSG101 among the three ESCRT-I components, suggesting that ALG-2 associates with hVps28 and hVps37A indirectly through TSG101. Using various deletion mutants of TSG101, the central PRR (proline-rich region) was found to be sufficient for interaction with ALG-2 by the GST-pull-down assay. Direct binding of ALG-2 to the TSG101 PRR was demonstrated by an overlay assay using biotin-labelled ALG-2 as a probe. In immunofluorescence microscopic analysis of HeLa cells that overexpressed a GFP (green fluorescent protein)-fused ATPase-defective dominant-negative form of SKD1/Vps4B (GFP-SKD1(E235Q)), ALG-2 exhibited a punctate distribution at the perinuclear area and co-localized with GFP-SKD1(E235Q) to aberrant endosomes. This punctate distribution of ALG-2 was markedly diminished by treatment of HeLa cells with a membrane-permeant Ca2+ chelator. Moreover, a Ca2+-binding-defective mutant of ALG-2 did not co-localize with GFP-SKD1(E235Q). Our findings suggest that ALG-2 may function as a Ca2+-dependent accessory protein of the endosomal sorting machinery by interacting directly with TSG101 as well as with Alix.
ALG-2(凋亡相关基因2)是一种钙结合蛋白,属于PEF(五EF手型)蛋白家族。其结合伴侣之一Alix(ALG-2相互作用蛋白X)/AIP1(ALG-2相互作用蛋白1)与TSG101和CHMP4(带电多泡体蛋白4)相互作用,它们分别是运输所需内体分选复合物I(ESCRT-I)和ESCRT-III的组成成分。在本研究中,我们调查了ALG-2与ESCRT-I之间的关联。通过使用HEK-293T(人胚肾293T)细胞裂解物进行的GST(谷胱甘肽S-转移酶)下拉实验,发现在有Ca2+存在的情况下,内源性TSG101以及另外两种外源表达的ESCRT-I成分[hVps28(人液泡蛋白分选28)和hVps37A]与GST-ALG-2相关联。然而,通过酵母双杂交实验,在三种ESCRT-I成分中仅观察到TSG101有阳性相互作用,这表明ALG-2通过TSG101间接与hVps28和hVps37A相关联。使用TSG101的各种缺失突变体,通过GST下拉实验发现中央富含脯氨酸区域(PRR)足以与ALG-2相互作用。使用生物素标记的ALG-2作为探针的覆盖实验证明了ALG-2与TSG101 PRR的直接结合。在对过表达GFP(绿色荧光蛋白)融合的ATP酶缺陷型显性负性形式的SKD1/Vps4B(GFP-SKD1(E235Q))的HeLa细胞进行免疫荧光显微镜分析时,ALG-2在核周区域呈现点状分布,并与GFP-SKD1(E235Q)共定位于异常内体。用膜通透性钙螯合剂处理HeLa细胞后,ALG-2的这种点状分布明显减少。此外,ALG-2的钙结合缺陷型突变体不与GFP-SKD1(E235Q)共定位。我们的研究结果表明,ALG-2可能通过直接与TSG101以及Alix相互作用,作为内体分选机制的钙依赖性辅助蛋白发挥作用。