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苦苣菜黄网病毒基因组RNA末端区域的序列分析

Sequence analysis of the trailer region of sonchus yellow net virus genomic RNA.

作者信息

Choi T J, Wagner J D, Jackson A O

机构信息

Department of Plant Biology, University of California, Berkeley 94720.

出版信息

Virology. 1994 Jul;202(1):33-40. doi: 10.1006/viro.1994.1319.

Abstract

The sequence of the 5' terminus (or the "trailer" region) of the minus-sense RNA genome of sonchus yellow net virus (SYNV) was determined by dideoxynucleotide termination sequencing of purified viral RNA and cloned cDNAs. The 5'-terminal nucleotide was identified by nuclease P1 digestion of 32P-end-labeled genomic RNA followed by polyethyleneimine cellulose chromatography. The trailer sequence occupies positions 13,561 to 13,720 relative to the 3' end of the genomic RNA and is composed of 160 nucleotides (nt) adjacent to a dinucleotide forming a portion of the "gene junction" sequence at the terminus of the L protein gene. The trailer sequence is longer than the 144-nt plus-strand leader RNA transcribed from the 3' end of the genomic RNA and is the longest trailer sequence yet reported among the nonsegmented negative-strand viruses. As is characteristic of other rhabdovirus genomes, the 3' and 5' termini of the SYNV genome are complementary and are capable of forming a panhandle structure involving 16 of the 18 terminal nucleotides. However, there is no obvious direct nucleotide sequence relatedness between the SYNV trailer sequence and those of animal rhabdoviruses and paramyxoviruses. The existence of a minus-strand leader RNA of the same polarity as the trailer sequence could not be detected in nucleic acid extracted from infected plants under hybridization conditions suitable for detection of the plus-strand leader RNA. In this regard, SYNV differs from vesicular stomatitis virus and is similar to other rhabdoviruses which also fail to accumulate detectable minus-strand leader RNAs.

摘要

通过对纯化的病毒RNA和克隆的cDNA进行双脱氧核苷酸末端测序,确定了苣荬菜黄网病毒(SYNV)负义RNA基因组5'末端(或“尾区”)的序列。通过对32P末端标记的基因组RNA进行核酸酶P1消化,然后进行聚乙烯亚胺纤维素层析,鉴定了5'-末端核苷酸。相对于基因组RNA的3'末端,尾区序列占据第13561至13720位,由160个核苷酸(nt)组成,与一个二核苷酸相邻,该二核苷酸构成L蛋白基因末端“基因连接”序列的一部分。尾区序列比从基因组RNA的3'末端转录的144-nt正链前导RNA长,是迄今在非节段负链病毒中报道的最长的尾区序列。正如其他弹状病毒基因组的特征一样,SYNV基因组的3'和5'末端是互补的,能够形成一个涉及18个末端核苷酸中的16个的锅柄结构。然而,SYNV尾区序列与动物弹状病毒和副粘病毒的尾区序列之间没有明显的直接核苷酸序列相关性。在适合检测正链前导RNA的杂交条件下,从受感染植物中提取的核酸中未检测到与尾区序列极性相同的负链前导RNA的存在。在这方面,SYNV与水泡性口炎病毒不同,与其他也未能积累可检测到的负链前导RNA的弹状病毒相似。

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