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An Activity Associated with Human Chromosome 21 Permits Nuclear Colocalization of the Adenovirus E1B-55K and E4orf6 Proteins and Promotes Viral Late Gene Expression

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Journal J Virol
Date 2003 Jun 28
PMID 12829847
Citations 2
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Abstract

The adenovirus E1B-55K and E4orf6 proteins cooperate during virus infection while performing several tasks that contribute to a productive infection, including the selective nucleocytoplasmic transport of late viral mRNA. Previous studies have shown that the E4orf6 protein retains the E1B-55K protein in the nucleus of human and monkey cells, but not in those of rodents, suggesting that primate-specific cellular factors contribute to the E4orf6-mediated retention of the E1B-55K protein in the nucleus. In an effort to identify these proposed primate-specific cellular factors, the interaction of the E1B-55K and E4orf6 proteins was studied in a panel of stable human-rodent monochromosomal somatic cell hybrids. Analysis of this panel of cell lines has demonstrated the existence of an activity associated with human chromosome 21 that permits the E1B-55K and E4orf6 proteins to colocalize in the nucleus of a rodent cell. Additional hybrid cells bearing portions of human chromosome 21 were used to map this activity to a 10-megabase-pair segment of the chromosome, extending from 21q22.12 to a region near the q terminus. Strikingly, this region also facilitates the expression of adenovirus late genes in a rodent cell background while having little impact on the expression of early viral genes.

Citing Articles

RUNX1 permits E4orf6-directed nuclear localization of the adenovirus E1B-55K protein and associates with centers of viral DNA and RNA synthesis.

Marshall L, Moore A, Ohki M, Kitabayashi I, Patterson D, Ornelles D J Virol. 2008; 82(13):6395-408.

PMID: 18417565 PMC: 2447068. DOI: 10.1128/JVI.00043-08.


Both BC-box motifs of adenovirus protein E4orf6 are required to efficiently assemble an E3 ligase complex that degrades p53.

Blanchette P, Cheng C, Yan Q, Ketner G, Ornelles D, Dobner T Mol Cell Biol. 2004; 24(21):9619-29.

PMID: 15485928 PMC: 522240. DOI: 10.1128/MCB.24.21.9619-9629.2004.

References
1.
Bowles K, Gibson J, Wu J, Shaffer L, Towbin J, Bowles N . Genomic organization and chromosomal localization of the human Coxsackievirus B-adenovirus receptor gene. Hum Genet. 1999; 105(4):354-9. DOI: 10.1007/s004399900136. View

2.
Pedron J . Identification of intranuclear structures containing the 72K DNA-binding protein of human adenovirus type 5. Eur J Cell Biol. 1984; 34(2):313-22. View

3.
Kratzer F, Rosorius O, Heger P, HIRSCHMANN N, Dobner T, HAUBER J . The adenovirus type 5 E1B-55K oncoprotein is a highly active shuttle protein and shuttling is independent of E4orf6, p53 and Mdm2. Oncogene. 2000; 19(7):850-7. DOI: 10.1038/sj.onc.1203395. View

4.
Nevels M, Rubenwolf S, Spruss T, Wolf H, Dobner T . Two distinct activities contribute to the oncogenic potential of the adenovirus type 5 E4orf6 protein. J Virol. 2000; 74(11):5168-81. PMC: 110870. DOI: 10.1128/jvi.74.11.5168-5181.2000. View

5.
Harlow E, Franza Jr B, Schley C . Monoclonal antibodies specific for adenovirus early region 1A proteins: extensive heterogeneity in early region 1A products. J Virol. 1985; 55(3):533-46. PMC: 255001. DOI: 10.1128/JVI.55.3.533-546.1985. View