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Solution structure of stem-loop alpha of the hepatitis B virus post-transcriptional regulatory element

机译:乙型肝炎病毒转录后调控元件茎环α的溶液结构

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Chronic hepatitis B virus (HBV) infections may lead to severe diseases like liver cirrhosis or hepatocellular carcinoma (HCC). The HBV post-transcriptional regulatory element (HPRE) facilitates the nuclear export of unspliced viral mRNAs, contains a splicing regulatory element and resides in the 3'-region of all viral transcripts. The HPRE consists of three sub-elements alpha (nucleotides 1151-1346), beta 1(nucleotides 1347-1457) and beta 2 (nucleotides 1458-1582), which confer together full export competence. Here, we present the NMR solution structure (pdb 2JYM) of the stem-loop alpha (SL alpha nucleotides 1292-1321) located in the sub-element . The SL alpha contains a CAGGC pentaloop highly conserved in hepatoviruses, which essentially adopts a CUNG-like tetraloop conformation. Furthermore, the SL alpha harbours a single bulged G residue flanked by A-helical regions. The structure is highly suggestive of serving two functions in the context of export of unspliced viral RNA: binding sterile alpha motif (SAM-) domain containing proteins and/or preventing the utilization of a 3'-splice site contained within SL alpha.
机译:慢性乙型肝炎病毒(HBV)感染可能导致严重的疾病,例如肝硬化或肝细胞癌(HCC)。 HBV转录后调控元件(HPRE)促进了未剪接病毒mRNA的核输出,包含一个剪接调控元件,并位于所有病毒转录本的3'区。 HPRE由三个子元素alpha(核苷酸1151-1346),beta 1(核苷酸1347-1457)和beta 2(核苷酸1458-1582)组成,它们共同赋予了全部出口能力。在这里,我们介绍位于子元素中的茎环α(SLα核苷酸1292-1321)的NMR溶液结构(pdb 2JYM)。 SL alpha包含在肝病毒中高度保守的CAGGC pentaloop,其本质上采用CUNG样四环构象。此外,SLα带有单个凸起的G残基,两侧是A螺旋区。该结构强烈提示在未剪接的病毒RNA的输出中起两种作用:结合含有无菌α模体(SAM-)的蛋白质和/或阻止SLα中包含的3'剪接位点的利用。

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