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Sprouty 2 结合 ESCRT-II 因子 Eap20 并促进 HIV-1 gag 释放。

Sprouty 2 binds ESCRT-II factor Eap20 and facilitates HIV-1 gag release.

机构信息

Life Sciences Bldg., Rm. 248, Department of Molecular Genetics & Microbiology, Stony Brook University, Stony Brook, NY 11794-5222, USA.

出版信息

J Virol. 2011 Jul;85(14):7353-62. doi: 10.1128/JVI.00141-11. Epub 2011 May 4.

Abstract

The four ESCRT (endocytic sorting complexes required for transport) complexes (ESCRT-0, -I, -II, and -III) normally operate sequentially in the trafficking of cellular cargo. HIV-1 Gag trafficking and release as virus-like particles (VLPs) require the participation of ESCRTs; however, its use of ESCRTs is selective and nonsequential. Specifically, Gag trafficking to release sites on the plasma membrane does not require ESCRT-0 or -II. It is known that a bypass of ESCRT-0 is achieved by the direct linkage of the ESCRT-I component, Tsg101, to the primary L domain motif (PTAP) in Gag and that bypass of ESCRT-II is achieved by the linkage of Gag to ESCRT-III through the adaptor protein Alix. However, the mechanism by which Gag suppresses the interaction of bound ESCRT-I with ESCRT-II is unknown. Here we show (i) that VLP release requires the steady-state level of Sprouty 2 (Spry2) in COS-1 cells, (ii) that Spry2 binds the ESCRT-II component Eap20, (iii) that binding Eap20 permits Spry2 to disrupt ESCRT-I interaction with ESCRT-II, and (iv) that coexpression of Gag with a Spry2 fragment that binds Eap20 increases VLP release. Spry2 also facilitated release of P7L-Gag (i.e., release in the absence of Tsg101 binding). In this case, rescue required the secondary L domain (YPX(n)L) in HIV-1 Gag that binds Alix and the region in Spry2 that binds Eap20. The results identify Spry2 as a novel cellular factor that facilitates release driven by the primary and secondary HIV-1 Gag L domains.

摘要

四个内体分选复合物(ESCRT,endocytic sorting complexes required for transport)(ESCRT-0、-I、-II 和 -III)通常在细胞货物运输中按顺序运作。HIV-1 Gag 运输和作为病毒样颗粒(VLPs)释放需要 ESCRTs 的参与;然而,其对 ESCRTs 的利用是有选择性的,而且是非连续的。具体来说,Gag 向质膜上的释放部位的运输不需要 ESCRT-0 或 -II。已知 ESCRT-I 成分 Tsg101 与 Gag 中的主要 L 结构域基序(PTAP)的直接连接绕过了 ESCRT-0,而 Gag 通过衔接蛋白 Alix 与 ESCRT-III 的连接绕过了 ESCRT-II。然而,Gag 抑制结合的 ESCRT-I 与 ESCRT-II 相互作用的机制尚不清楚。在这里,我们展示了:(i)VLPs 的释放需要 COS-1 细胞中 Sprouty 2(Spry2)的稳态水平;(ii)Spry2 结合 ESCRT-II 成分 Eap20;(iii)结合 Eap20 允许 Spry2 破坏 ESCRT-I 与 ESCRT-II 的相互作用;(iv)Gag 与结合 Eap20 的 Spry2 片段的共表达增加了 VLP 的释放。Spry2 还促进了 P7L-Gag 的释放(即,在没有 Tsg101 结合的情况下释放)。在这种情况下,拯救需要 HIV-1 Gag 中的二级 L 结构域(YPX(n)L),该结构域与 Alix 结合,以及与 Spry2 结合的 Eap20 区域。结果表明,Spry2 是一种新的细胞因子,可促进由 HIV-1 Gag 的主要和次要 L 结构域驱动的释放。

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