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乳酸脱氢酶升高病毒基因组序列:P株和C株之间的异质性

Sequence of the genome of lactate dehydrogenase-elevating virus: heterogenicity between strains P and C.

作者信息

Palmer G A, Kuo L, Chen Z, Faaberg K S, Plagemann P G

机构信息

Department of Microbiology, University of Minnesota Medical School, Minneapolis 55455, USA.

出版信息

Virology. 1995 Jun 1;209(2):637-42. doi: 10.1006/viro.1995.1296.

Abstract

The complete nucleotide sequence of genomic RNA (14104 nt) of one strain of lactate dehydrogenase-elevating virus (LDV), LDV-P, is reported. It exhibits only about 80% nucleotide identity with the sequence reported for another LDV strain, LDV-C (Godeny et al., Virology 194, 585-596 (1993), and is 68 nucleotides shorter than the reported LDV-C sequence. The difference in length is largely due to the lack of a 59-nucleotide-long direct repeat in ORF 1a of the reported LDV-C sequence. Sequence analysis of a total of 1.4 kb of ORF 1a of LDV-C via reverse transcription/polymerase chain reaction (RT/PCR) technology failed to confirm the presence of this repeat in the LDV-C genome as well as of 24 deletions/insertions of single nucleotides that give rise to apparent transient reading frame differences between the LDV-P and LDV-C genomes and might have represented frameshift mutations. An additional 35 nucleotides in ORF 1a of the RT/PCR LDV-C products were the same as in the LDV-P rather than the reported LDV-C genome. The nucleotide sequences of the 5' leader and the 3' noncoding ends of the two genomes and the heptanucleotides involved in joining the 5' leader to the bodies of the subgenomic mRNAs were highly conserved or identical. The predicted LDV-P proteins, however, differed from those predicted for the LDV-C proteins between 25% for the ORF 2 protein and 1% for the ORF 7 nucleocapsid protein. All functional motifs of the ORF 1a and ORF 1b proteins were conserved. The ORF 1a protein possesses 11 potential transmembrane segments that flank the serine protease domain.

摘要

报道了一株乳酸脱氢酶升高病毒(LDV)——LDV-P基因组RNA(14104个核苷酸)的完整核苷酸序列。它与另一株LDV——LDV-C报道的序列仅约有80%的核苷酸同一性(戈德尼等人,《病毒学》194卷,585 - 596页(1993年)),并且比报道的LDV-C序列短68个核苷酸。长度差异主要是由于报道的LDV-C序列的开放阅读框1a中缺少一个59个核苷酸长的直接重复序列。通过逆转录/聚合酶链反应(RT/PCR)技术对LDV-C的总共1.4kb的开放阅读框1a进行序列分析,未能证实该重复序列在LDV-C基因组中的存在,也未证实有24个单核苷酸的缺失/插入,这些缺失/插入导致LDV-P和LDV-C基因组之间出现明显的瞬时阅读框差异,可能代表移码突变。RT/PCR LDV-C产物的开放阅读框1a中另外35个核苷酸与LDV-P中的相同,而不是与报道的LDV-C基因组中的相同。两个基因组的5'前导序列和3'非编码末端的核苷酸序列以及参与将5'前导序列连接到亚基因组mRNA主体的七核苷酸高度保守或相同。然而,预测的LDV-P蛋白与预测的LDV-C蛋白不同,开放阅读框2蛋白的差异为25%,开放阅读框7核衣壳蛋白的差异为1%。开放阅读框1a和开放阅读框1b蛋白的所有功能基序都是保守的。开放阅读框1a蛋白拥有11个潜在的跨膜区段,位于丝氨酸蛋白酶结构域两侧。

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