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Literature DB >> 1312123

Nucleotide sequences of normal and rearranged RNA segments 10 of human rotaviruses.

Abstract

Normal and rearranged RNA segments 10 of group A rotaviruses isolated from a chronically infected immunodeficient child were amplified by the polymerase chain reaction as full-length cDNA copies, and were subsequently cloned and sequenced. Compared with the nucleotide sequence of the normal RNA segment 10, the rearranged form contains a partial non-coding duplication at its 3' end and several point mutations. The normal RNA segment 10 was similar to that of bovine rotavirus.

Entities: Disease Species

Mesh：

Substances：
RNA, Viral

Year: 1992 PMID： 1312123 DOI： 10.1099/0022-1317-73-3-633

Source DB: PubMed Journal: J Gen Virol ISSN： 0022-1317 Impact factor: 3.891

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Cited

22 in total

1. A human rotavirus with rearranged genes 7 and 11 encodes a modified NSP3 protein and suggests an additional mechanism for gene rearrangement.

Authors: E Gault; N Schnepf; D Poncet; A Servant; S Teran; A Garbarg-Chenon
Journal: J Virol Date: 2001-08 Impact factor: 5.103

2. Nondefective rotavirus mutants with an NSP1 gene which has a deletion of 500 nucleotides, including a cysteine-rich zinc finger motif-encoding region (nucleotides 156 to 248), or which has a nonsense codon at nucleotides 153-155.

Authors: K Taniguchi; K Kojima; S Urasawa
Journal: J Virol Date: 1996-06 Impact factor: 5.103

3. Sequence analysis demonstrates that VP6, NSP1 and NSP4 genes of Indian neonatal rotavirus strain 116E are of human origin.

Authors: N A Cunliffe; B K Das; M Ramachandran; M K Bhan; R I Glass; J R Gentsch
Journal: Virus Genes Date: 1997 Impact factor: 2.332

4. Rotavirus variant replicates efficiently although encoding an aberrant NSP3 that fails to induce nuclear localization of poly(A)-binding protein.

Authors: Michelle M Arnold; Catie Small Brownback; Zenobia F Taraporewala; John T Patton
Journal: J Gen Virol Date: 2012-03-21 Impact factor: 3.891

5. Generation of genetically stable recombinant rotaviruses containing novel genome rearrangements and heterologous sequences by reverse genetics.

Authors: Aitor Navarro; Shane D Trask; John T Patton
Journal: J Virol Date: 2013-03-27 Impact factor: 5.103

Nucleotide sequences of normal and rearranged RNA segments 10 of human rotaviruses.

1. A human rotavirus with rearranged genes 7 and 11 encodes a modified NSP3 protein and suggests an additional mechanism for gene rearrangement.

2. Nondefective rotavirus mutants with an NSP1 gene which has a deletion of 500 nucleotides, including a cysteine-rich zinc finger motif-encoding region (nucleotides 156 to 248), or which has a nonsense codon at nucleotides 153-155.

3. Sequence analysis demonstrates that VP6, NSP1 and NSP4 genes of Indian neonatal rotavirus strain 116E are of human origin.

4. Rotavirus variant replicates efficiently although encoding an aberrant NSP3 that fails to induce nuclear localization of poly(A)-binding protein.

5. Generation of genetically stable recombinant rotaviruses containing novel genome rearrangements and heterologous sequences by reverse genetics.

6. Sequence analysis of the NSP4 gene from human rotavirus strains isolated in the United States.

7. A rearranged genomic segment 11 is common to different human rotaviruses.

8. Rearrangement of the VP6 gene of a group A rotavirus in combination with a point mutation affecting trimer stability.

9. Group A human rotavirus genomics: evidence that gene constellations are influenced by viral protein interactions.

10. RNA structure and heterologous recombination in the double-stranded RNA bacteriophage phi 6.