Molecular cloning and sequencing of the region of the Rubella virus genome coding for glycoprotein E1
The sequence of the 1600 3′ terminal nucleotides of the RNA of rubella virus was determined from cDNA synthesized from both virion and intracellular RNA using reverse transcriptase and an oligodeoxythymidine primer and cloned into a bacterial plasmid vector. This sequence contained the complete codi...
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Published in | Virology (New York, N.Y.) Vol. 154; no. 1; pp. 228 - 232 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
San Diego, CA
Elsevier Inc
15.10.1986
Elsevier |
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Abstract | The sequence of the 1600 3′ terminal nucleotides of the RNA of rubella virus was determined from cDNA synthesized from both virion and intracellular RNA using reverse transcriptase and an oligodeoxythymidine primer and cloned into a bacterial plasmid vector. This sequence contained the complete coding sequence for virion envelope protein E1 and a 57 nucleotide nontranslated region between the stop codon for E1 and the poly A tract. The predicted size for E1 was 481 amino acids and within this sequence were three potential N-linked glycosylation sites and a putative trans-membrane domain near the carboxy terminus. Immediately preceding the E1 coding region was a putative signal sequence. No homology was found at either the amino acid or nucleotide level between the region of the rubella virus genome sequenced and corresponding regions of the genomes of the alphaviruses, the other genus of the family Togaviridae for which sequence information has been obtained. |
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AbstractList | The sequence of the 1600 3′ terminal nucleotides of the RNA of rubella virus was determined from cDNA synthesized from both virion and intracellular RNA using reverse transcriptase and an oligodeoxythymidine primer and cloned into a bacterial plasmid vector. This sequence contained the complete coding sequence for virion envelope protein E1 and a 57 nucleotide nontranslated region between the stop codon for E1 and the poly A tract. The predicted size for E1 was 481 amino acids and within this sequence were three potential N-linked glycosylation sites and a putative trans-membrane domain near the carboxy terminus. Immediately preceding the E1 coding region was a putative signal sequence. No homology was found at either the amino acid or nucleotide level between the region of the rubella virus genome sequenced and corresponding regions of the genomes of the alphaviruses, the other genus of the family Togaviridae for which sequence information has been obtained. The sequence of the 1600 3' terminal nucleotides of the RNA of rubella virus was determined from cDNA synthesized from both virion and intracellular RNA using reverse transcriptase and an oligodeoxythymidine primer and cloned into a bacterial plasmid vector. No homology was found at either the amino acid or nucleotide level between the region of the rubella virus genome sequenced and corresponding regions of the genomes of the alphaviruses, the other genus of the family Togaviridae for which sequence information has been obtained. |
Author | Marr, Lee D. Hemphill, Mark L. Frey, Teryl K. Dominguez, Geraldina |
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Keywords | Virus RNA Nucleotide sequence Rubivirus Togaviridae Glycoproteins Molecular cloning Rubella virus |
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Snippet | The sequence of the 1600 3′ terminal nucleotides of the RNA of rubella virus was determined from cDNA synthesized from both virion and intracellular RNA using... The sequence of the 1600 3' terminal nucleotides of the RNA of rubella virus was determined from cDNA synthesized from both virion and intracellular RNA using... |
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SubjectTerms | Amino Acid Sequence Base Sequence Biological and medical sciences Cloning, Molecular DNA - genetics DNA, Viral - genetics Fundamental and applied biological sciences. Psychology Genes, Viral Genetics Microbiology RNA, Viral - genetics rubella virus Rubella virus - genetics Virology |
Title | Molecular cloning and sequencing of the region of the Rubella virus genome coding for glycoprotein E1 |
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