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ITCH 蛋白在人类 T 细胞白血病病毒 1 型释放中的作用。

The role of ITCH protein in human T-cell leukemia virus type 1 release.

机构信息

HIV-Drug Resistance Program, NCI Frederick, Frederick, Maryland 21702, USA.

出版信息

J Biol Chem. 2011 Sep 9;286(36):31092-104. doi: 10.1074/jbc.M111.259945. Epub 2011 Jul 1.

Abstract

Human T-cell leukemia virus type 1 (HTLV-1) has two late domain (LD) motifs, PPPY and PTAP, which are important for viral budding. Mutations in the PPPY motif are more deleterious for viral release than changes in the PTAP motif. Several reports have shown that the interaction of PPPY with the WW domains of a Nedd4 (neuronal precursor cell-expressed developmentally down-regulated-4) family ubiquitin ligase (UL) is a critical event in virus release. We tested nine members of the Nedd4 family ULs and found that ITCH is the main contributor to HTLV-1 budding. ITCH overexpression strongly inhibited release and infectivity of wild-type (wt) HTLV-1, but rescued the release of infectious virions with certain mutations in the PPPY motif. Electron microscopy showed either fewer or misshapen virus particles when wt HTLV-1 was produced in the presence of overexpressed ITCH, whereas mutants with changes in the PPPY motif yielded normal looking particles at wt level. The other ULs had significantly weaker or no effects on HTLV-1 release and infectivity except for SMURF-1, which caused enhanced release of wt and all PPPY(-) mutant particles. These particles were poorly infectious and showed abnormal morphology by electron microscopy. Budding and infectivity defects due to overexpression of ITCH and SMURF-1 were correlated with higher than normal ubiquitination of Gag. Only silencing of ITCH, but not of WWP1, WWP2, and Nedd4, resulted in a reduction of HTLV-1 budding from 293T cells. The binding efficiencies between the HTLV-1 LD and WW domains of different ULs as measured by mammalian two-hybrid interaction did not correlate with the strength of their effect on HTLV-1 budding.

摘要

人类 T 细胞白血病病毒 1 型(HTLV-1)有两个晚期结构域(LD)基序,PPP Y 和 PTAP,这对于病毒出芽很重要。PPP Y 基序中的突变比 PTAP 基序中的突变对病毒释放更具危害性。有几项报告表明,PPP Y 与 Nedd4(神经前体细胞表达的发育下调 4)家族泛素连接酶(UL)的 WW 结构域的相互作用是病毒释放的关键事件。我们测试了 Nedd4 家族的 9 个 UL,发现 ITCH 是 HTLV-1 出芽的主要贡献者。ITCH 过表达强烈抑制野生型(wt)HTLV-1 的释放和感染性,但挽救了 PPP Y 基序中某些突变的感染性病毒粒子的释放。电子显微镜显示,当 wt HTLV-1 在过表达 ITCH 的存在下产生时,病毒粒子要么较少,要么形状异常,而 PPP Y 基序发生变化的突变体以 wt 水平产生正常外观的颗粒。除了 SMURF-1 之外,其他 UL 对 HTLV-1 的释放和感染性没有明显的影响,SMURF-1 导致 wt 和所有 PPP Y(-)突变体颗粒的释放增强。这些颗粒的感染性很差,电子显微镜下显示出异常形态。由于 ITCH 和 SMURF-1 的过表达导致的出芽和感染缺陷与 Gag 的泛素化水平高于正常水平相关。只有 ITCH 的沉默,而不是 WWP1、WWP2 和 Nedd4 的沉默,导致从 293T 细胞中减少 HTLV-1 的出芽。通过哺乳动物双杂交相互作用测量的 HTLV-1 LD 和不同 UL 的 WW 结构域之间的结合效率与它们对 HTLV-1 出芽的影响强度没有相关性。

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本文引用的文献

1
Functional interchangeability of late domains, late domain cofactors and ubiquitin in viral budding.
PLoS Pathog. 2010 Oct 21;6(10):e1001153. doi: 10.1371/journal.ppat.1001153.
4
Quantitative comparison of HTLV-1 and HIV-1 cell-to-cell infection with new replication dependent vectors.
PLoS Pathog. 2010 Feb 26;6(2):e1000788. doi: 10.1371/journal.ppat.1000788.
5
Late domain-independent rescue of a release-deficient Moloney murine leukemia virus by the ubiquitin ligase itch.
J Virol. 2010 Jan;84(2):704-15. doi: 10.1128/JVI.01319-09. Epub 2009 Oct 28.
6
Physiological functions of the HECT family of ubiquitin ligases.
Nat Rev Mol Cell Biol. 2009 Jun;10(6):398-409. doi: 10.1038/nrm2690. Epub 2009 May 13.
7
The ESCRT machinery in endosomal sorting of ubiquitylated membrane proteins.
Nature. 2009 Mar 26;458(7237):445-52. doi: 10.1038/nature07961.
9
The ESCRT machinery: new functions in viral and cellular biology.
Biochem Soc Trans. 2009 Feb;37(Pt 1):195-9. doi: 10.1042/BST0370195.
10
The ESCRT pathway and HIV-1 budding.
Biochem Soc Trans. 2009 Feb;37(Pt 1):181-4. doi: 10.1042/BST0370181.

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