Expression and Packaging of a Human Endogenous Retrovirus-K Genomic DNA Clone.
10.4167/jbv.2006.36.4.237
- Author:
Young Mie HA-LEE
1
Author Information
1. Department of Molecular Biology and Microbiology Tufts University School of Medicine 136 Harrison Avenue, Boston, MA 02111, USA. ymhalee@yonsei.ac.kr
- Publication Type:Original Article
- Keywords:
HERV-K;
Genome;
Gag;
Expression;
Packaging
- MeSH:
Autoimmune Diseases;
Capsid Proteins;
Cell Line;
Clinical Coding;
Clone Cells*;
DNA*;
Endogenous Retroviruses;
Genome;
Genome, Human;
Humans*;
Nuclear Export Signals;
Product Packaging*;
Proviruses;
Retroviridae;
RNA;
Transfection
- From:Journal of Bacteriology and Virology
2006;36(4):237-245
- CountryRepublic of Korea
- Language:English
-
Abstract:
Human contains large number of human endogenous retroviruses (HERVs) in its genome. One of the HERV families, HERV-K, entered human genome most recently and includes many members with full-length intact proviruses. Normally, these proviruses do not express but infrequently they seem to express in cancers or autoimmune disease patients. To investigate expression mechanisms of these endogenous retroviruses, a DNA copy of HERV-K was cloned and its expression was studied. The transfection of the full-length clone into human cell lines did not produce any detectable viral capsid protein, Gag, and the transcription from its own promoter in LTR was extremely poor. The transcription was less than 10 percent compare to the exogenous retrovirus. However, when the Gag coding region was cloned under CMV promoter, Gag could be expressed efficiently and secreted as particles, probably virus like particles. The efficient expression also required a nuclear export signal. The expressed Gag could also package its own genomic RNA. These results indicate that the LTR of HERV-K is normally not active but its genes have a potential to express and possibly produce infectious particles.
