Human T-cell leukemia virus type 1 (HTLV-1) encodes a 40-kDa Tax phosphoprotein. Tax is a transcriptional activator which modulates expression of the viral long terminal repeat and transcription of many cellular genes. Because Tax is a critical HTLV-1 factor which mediates viral transformation of T cells during the genesis of adult T-cell leukemia, it is important to understand the processes which can activate or inactivate Tax function. Here, we report that ubiquitination of Tax is a posttranscriptional mechanism which regulates Tax function. We show that ubiquitination does not target Tax for degradation by the proteasome. Rather, ubiquitin addition modifies Tax in a proteasome-independent manner from an active to a less-active transcriptional form.
Ubiquitination of human T-cell leukemia virus type 1 tax modulates its activity.
人类T细胞白血病病毒1型Tax蛋白的泛素化调节其活性
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作者:Peloponese Jean-Marie Jr, Iha Hidekatsu, Yedavalli Venkat R K, Miyazato Akiko, Li Yan, Haller Kerstin, Benkirane Monsef, Jeang Kuan-Teh
| 期刊: | Journal of Virology | 影响因子: | 3.800 |
| 时间: | 2004 | 起止号: | 2004 Nov;78(21):11686-95 |
| doi: | 10.1128/JVI.78.21.11686-11695.2004 | 种属: | Human |
| 研究方向: | 细胞生物学 | 疾病类型: | 白血病 |
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