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乙型肝炎病毒X蛋白的生物化学与功能

Biochemistry and functions of hepatitis B virus X protein.

作者信息

Koike K, Takada S

机构信息

Department of Gene Research, Cancer Institute, Tokyo, Japan.

出版信息

Intervirology. 1995;38(1-2):89-99. doi: 10.1159/000150417.

Abstract

Hepatitis B virus X gene codes for a small basic cytoplasmic protein and is able to transactivate viral and cellular genes, although X protein exhibits no DNA-binding activity. The mechanism of transactivation by X protein has been suggested to be via protein-protein interaction(s). X protein had amino acid sequences homologous to the functionally essential domain of Kunitz-type serine protease inhibitors, and these sequences were indispensable for transactivation function. X protein activated X-gene transcription itself and an X-responsive element were localized in their minimal promoter. Furthermore, tumor suppressor gene product p53, but not mutant p53, repressed X-gene transcription from the minimal promoter, indicating that X protein disrupts the function of normal p53, which represses transcription of X gene or cellular gene. Data suggest that inhibition of a hepatic serine protease by X protein leads to eliminate the suppressor effect of p53 on the basic transcription machinery in nucleus.

摘要

乙型肝炎病毒X基因编码一种小的碱性细胞质蛋白,尽管X蛋白不具有DNA结合活性,但它能够反式激活病毒和细胞基因。X蛋白的反式激活机制被认为是通过蛋白质-蛋白质相互作用实现的。X蛋白具有与Kunitz型丝氨酸蛋白酶抑制剂功能必需结构域同源的氨基酸序列,这些序列对于反式激活功能是不可或缺的。X蛋白自身激活X基因转录,并且一个X反应元件定位在其最小启动子中。此外,肿瘤抑制基因产物p53而非突变型p53抑制了最小启动子的X基因转录,这表明X蛋白破坏了正常p53的功能,而正常p53可抑制X基因或细胞基因的转录。数据表明,X蛋白对肝脏丝氨酸蛋白酶的抑制作用导致消除了p53对细胞核中基础转录机制的抑制作用。

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