The hepatitis B virus post transcriptional regulatory element contains a highly stable RNA secondary structure

被引:18
作者
Patzel, V [1 ]
Sczakiel, G [1 ]
机构
[1] DEUTSCH KREBSFORSCHUNGSZENTRUM, FORSCH SCHWERPUNKT ANGEW TUMORVIROL, D-69120 HEIDELBERG, GERMANY
关键词
D O I
10.1006/bbrc.1997.6205
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatitis B virus (HBV) transcripts contain a sequence known as the posttranscriptional regulatory element (PRE). This element was shown to facilitate the nuclear export of the S gene transcripts, to partially substitute for the human immunodeficiency virus (HIV-1) Rev-response element (RRE), and to bind two cellular factors, Within the genetically defined PRE (approximately 450 nucleotides), we identified a highly stable secondary structural element of 313 nucleotides in length termed PRE(313). The energy values of the PRE(313) are similar to those of the RRE of HIV-1 and significantly lower than those of other portions of HBV RNA. A comparison of human HBV subtypes shows strong conservation of the PRE(313) in terms of energy and structure, providing further evidence for the biological significance of the genetically defined PRE and the PRE(313) in particular. The structural model for the PRE(313) described in this study may help in identifying crucial components of the transport mechanism of transcripts of HBV. (C) 1997 Academic Press.
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页码:864 / 867
页数:4
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