Quarleri Jorge
Jorge Quarleri, Instituto de Investigaciones Biomédicas en Retrovirus y Sida, Universidad de Buenos Aires, CONICET, Buenos Aires C1121ABG, Argentina.
World J Gastroenterol. 2014 Jan 14;20(2):425-35. doi: 10.3748/wjg.v20.i2.425.
The core promoter (CP) of the viral genome plays an important role for hepatitis B virus (HBV) replication as it directs initiation of transcription for the synthesis of both the precore and pregenomic (pg) RNAs. The CP consists of the upper regulatory region and the basal core promoter (BCP). The CP overlaps with the 3'-end of the X open reading frames and the 5'-end of the precore region, and contains cis-acting elements that can independently direct transcription of the precore mRNA and pgRNA. Its transcription regulation is under strict control of viral and cellular factors. Even though this regulatory region exhibits high sequence conservation, when variations appear, they may contribute to the persistence of HBV within the host, leading to chronic infection and cirrhosis, and eventually, hepatocellular carcinoma. Among CP sequence variations, those occurring at BCP may dysregulate viral gene expression with emphasis in the hepatitis B e antigen, and contribute to disease progression. In this review these molecular aspects and pathologic topics of core promoter are deeply evaluated.
病毒基因组的核心启动子(CP)对乙型肝炎病毒(HBV)复制起着重要作用,因为它指导前核心RNA和前基因组(pg)RNA合成的转录起始。CP由上游调控区和基础核心启动子(BCP)组成。CP与X开放阅读框的3'端和前核心区的5'端重叠,并包含可独立指导前核心mRNA和pgRNA转录的顺式作用元件。其转录调控受到病毒和细胞因子的严格控制。尽管该调控区表现出高度的序列保守性,但当出现变异时,它们可能有助于HBV在宿主体内的持续存在,导致慢性感染和肝硬化,并最终引发肝细胞癌。在CP序列变异中,那些发生在BCP的变异可能会失调病毒基因表达,尤其是乙型肝炎e抗原,并促进疾病进展。在这篇综述中,对核心启动子的这些分子方面和病理主题进行了深入评估。