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鸭乙型肝炎病毒衣壳前基因组RNA 3'区域的代表性不足。

Underrepresentation of the 3' region of the capsid pregenomic RNA of duck hepatitis B virus.

作者信息

Ostrow Kristin M, Loeb Daniel D

机构信息

McArdle Laboratory for Cancer Research, University of Wisconsin Medical School, Madison, Wisconsin 53706, USA.

出版信息

J Virol. 2004 Mar;78(5):2179-86. doi: 10.1128/jvi.78.5.2179-2186.2004.

Abstract

The pregenomic RNA (pgRNA) of hepadnaviruses is packaged into capsids where it is reverse transcribed to yield mature DNA genomes. This report describes differences between the 3' region and other regions of the pgRNA isolated from capsids. Analysis of capsid pgRNA isolated by using an established method involving micrococcal nuclease treatment demonstrated reduced levels of the 3' region of the pgRNA compared to the 5' region. This underrepresentation of the 3' region was partly a result of microccocal nuclease digestion of the 3' region because isolation of capsid pgRNA by an alternative method that did not involve nuclease treatment led to a greater, but not complete, recovery of the 3' region. These results indicate that the 3' region of the capsid pgRNA is susceptible to micrococcal nuclease digestion during its isolation and that the 3' region can still be underrepresented when capsid pgRNA is isolated without nuclease digestion. Additional experiments show that the 3' ends of capsid pgRNA isolated by micrococcal nuclease treatment are heterogeneously dispersed from nucleotide 2577 to the poly(A) tail. These data provide evidence that the 3' region of the capsid pgRNA has biochemical properties different from those of its 5' region. Possibly, the 3' region of the pgRNA is not packaged into the interior of the capsid but rather is associated with a part of the capsid where it is susceptible to microccocal nuclease digestion.

摘要

嗜肝DNA病毒的前基因组RNA(pgRNA)被包装进衣壳,在其中进行逆转录以产生成熟的DNA基因组。本报告描述了从衣壳中分离出的pgRNA的3'区域与其他区域之间的差异。通过使用涉及微球菌核酸酶处理的既定方法分离衣壳pgRNA进行分析,结果表明与5'区域相比,pgRNA的3'区域水平降低。3'区域的这种代表性不足部分是由于微球菌核酸酶对3'区域的消化,因为通过不涉及核酸酶处理的替代方法分离衣壳pgRNA导致3'区域的回收率更高但不完全。这些结果表明,衣壳pgRNA的3'区域在分离过程中易受微球菌核酸酶消化,并且在不进行核酸酶消化分离衣壳pgRNA时,3'区域仍可能代表性不足。额外的实验表明,通过微球菌核酸酶处理分离的衣壳pgRNA的3'末端从核苷酸2577到聚(A)尾是异质分散的。这些数据提供了证据,证明衣壳pgRNA的3'区域具有与其5'区域不同的生化特性。可能,pgRNA的3'区域没有被包装进衣壳内部,而是与衣壳的一部分相关联,在那里它易受微球菌核酸酶消化。

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