Chang J, Moraleda G, Gudima S, Taylor J
Fox Chase Cancer Center, Philadelphia, Pennsylvania 19111-2497, USA.
J Virol. 2000 Nov;74(21):9889-94. doi: 10.1128/jvi.74.21.9889-9894.2000.
Examination of the 1,679-nucleotide (nt) unit-length hepatitis delta virus (HDV) RNAs in the livers of two HDV-infected woodchucks showed that 96% of the antigenomic RNA but only 50% of the genomic RNA was circular. We subsequently found that at least half of the linear unit-length genomic RNA was open at a unique location. Using a modified form of RNA ligation-mediated amplification of cDNA ends, we showed that the 5' end was located at nt 1212. Like the previously described ribozyme cleavage site at nt 686, the new site produced a 5'-OH. Nevertheless, we showed that this novel site was not produced by activity of the HDV genomic ribozyme. We speculate that the 5' end at nt 1212 reflects a preferred site of posttranscriptional endonucleolytic cleavage of genomic RNA.
对两只感染丁型肝炎病毒(HDV)的土拨鼠肝脏中1679个核苷酸(nt)单位长度的HDV RNA进行检测发现,反基因组RNA的96%呈环状,但基因组RNA只有50%呈环状。随后我们发现,至少一半的线性单位长度基因组RNA在一个独特位置是开放的。使用一种改良形式的RNA连接介导的cDNA末端扩增方法,我们发现5'端位于第1212个核苷酸处。与之前描述的位于第686个核苷酸处的核酶切割位点一样,新位点产生一个5'-OH。然而,我们发现这个新位点并非由HDV基因组核酶的活性产生。我们推测,第1212个核苷酸处的5'端反映了基因组RNA转录后内切核酸酶切割的一个优先位点。