首页> 美国卫生研究院文献>Journal of Virology >Polyoma Virus DNA: Complete Nucleotide Sequence of the Gene Which Codes for Polyoma Virus Capsid Protein VP1 and Overlaps the VP2/VP3 Genes
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Polyoma Virus DNA: Complete Nucleotide Sequence of the Gene Which Codes for Polyoma Virus Capsid Protein VP1 and Overlaps the VP2/VP3 Genes

机译:多瘤病毒DNA:编码多瘤病毒衣壳蛋白VP1且与VP2 / VP3基因重叠的基因的完整核苷酸序列

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摘要

The nucleotide sequence of part of the late region of the polyoma virus genome was determined. It contains coding information for the major capsid protein VP1 and the C-terminal region of the minor proteins VP2 and VP3. In the sequence with the same polarity as late mRNA's, all coding frames are blocked by termination codons in a region around 48 units on the physical map. This is the region where the N-terminus of VP1 and the C-termini of VP2 and VP3 have been located (T. Hunter and W. Gibson, J. Virol. >28:240-253, 1978; S. G. Siddell and A. E. Smith, J. Virol. >27:427-431, 1978; Smith et al., Cell >9:481-487, 1976). There are two long uninterrupted coding frames in the late region of polyoma virus DNA. One lies at the 5′ end of the sequence and contains potential coding sequences for VP2 and VP3. The other contains 383 consecutive sense codons starting with the ATG at nucleotide position 1,218, extends from 47.5 to 25.8 units counterclockwise on the physical map, and is located where the VP1 gene has been mapped. The VP1 gene overlaps the genes for proteins VP2/VP3 by 32 nucleotides and uses a different coding frame. From the DNA sequence, the amino acid sequence of VP1 was predicted. The proposed VP1 sequence is in good agreement with other data, namely, with the partial N-terminal amino acid sequence and the total amino acid composition. The VP1 coding frame terminates with a TAA codon at 25.8 map units. This is followed by an AATAAA sequence, which may act as a processing signal for the viral late mRNA's. When both nucleotide and amino acid sequences are compared with their counterparts in the related simian virus 40, extensive homologies are found over the entire region of the two viral genomes. Maximum homology appears to occur in those regions which code for the C-termini of the VP1 proteins. The overlap region of VP1 with VP2/VP3 of polyoma virus is shorter by 90 nucleotides than is that of simian virus 40 and shows very limited homology with the simian virus 40 sequence. This leads to the suggestion that the overlap segments of both viruses have been freed from stringency imposed on drifting during evolution and that proteins VP2 and VP3 of polyoma virus may have been truncated by the appearance of a termination codon within the sequence.
机译:确定了多瘤病毒基因组的晚期区域的一部分的核苷酸序列。它包含主要衣壳蛋白VP1和次要蛋白VP2和VP3的C端区域的编码信息。在具有与晚期mRNA相同极性的序列中,所有编码框架均被物理图谱上48个单位附近区域中的终止密码子所封闭。这是VP1的N端以及VP2和VP3的C末端所在的区域(T. Hunter和W. Gibson,J。Virol。> 28 :240-253,1978年) ; SG Siddell和AE Smith,J。Virol。> 27 :427-431,1978; Smith等,Cell > 9 :481-487,1976)。在多瘤病毒DNA的晚期区域有两个较长的不间断编码框架。一个位于序列的5'末端,并包含VP2和VP3的潜在编码序列。另一个包含383个连续的有义密码子,起始于核苷酸位置1,218处的ATG,在物理图谱上逆时针从47.5延伸至25.8个单位,并且位于VP1基因的定位位置。 VP1基因与蛋白VP2 / VP3的基因重叠32个核苷酸,并使用不同的编码框架。根据DNA序列,可以预测VP1的氨基酸序列。提出的VP1序列与其他数据,即部分N-末端氨基酸序列和总氨基酸组成非常吻合。 VP1编码帧以25.8个图单元的TAA密码子终止。其后是AATAAA序列,其可以作为病毒后期mRNA的加工信号。当在相关的猿猴病毒40中比较核苷酸和氨基酸序列与它们的对应序列时,在两个病毒基因组的整个区域中发现了广泛的同源性。最大的同源性似乎发生在编码VP1蛋白的C末端的那些区域中。 VP1与多瘤病毒的VP2 / VP3的重叠区域比猿猴病毒40的重叠区域短90个核苷酸,并且显示出与猿猴病毒40序列的非常有限的同源性。这提示了这两种病毒的重叠部分已摆脱进化过程中施加于漂移的严格性,并且多瘤病毒的蛋白VP2和VP3可能已被序列中终止密码子的出现截断了。

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