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J Gen Virol 71 (1990), 1829-1833; DOI 10.1099/0022-1317-71-8-1829
© 1990 Society for General Microbiology

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A New Transcription Element in the JC Virus Enhancer

Taka-aki Tamura1, Atsuo Aoyama1,2,, Takafumi Inoue1, Masayuki Miura1,{dagger} and Katsuhiko Mikoshiba1,2,

1 Division of Behaviour and Neurobiology, National Institute for Basic Biology, Myodaiji-cho, Okazaki-444
and2 Division of Macromolecular Function, Institute for Protein Research, Osaka University, Suita-565, Japan

The enhancer of JC virus restricts its gene expression to the brain. In a previous study, we demonstrated an enhancer element, nuclear factor I (NFI) motif, in the middle of the enhancer. Here, we demonstrate that the NFI motif is a tissue-specific element. We further present a new tissue-specific element, SacI motif, just upstream from the NFI motif. These motifs showed transcriptional enhancement both in vitro and in vivo and acted upon a heterologous adenovirus major late promoter. DNase I footprint analyses demonstrated that the SacI motif bound to a brain nuclear factor, and that its binding region overlapped with the NFI motif. Gel shift experiments with the SacI motif revealed that the populations of SacI motif factors in the brain and HeLa cell extracts were different. Together with our previous findings about tissue-specific NFI-like factor(s), cooperation of NFI motif and SacI motif factors may be required for the strong brain specificity of the viral gene expression.

{dagger} Present address: Department of Physiology, Keio University School of Medicine, Shinjuku-ku, Tokyo-160, Japan.

Received 19 December 1989; accepted 9 April 1990.


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F. K. Bedford, D. Julius, and H. A. Ingraham
Neuronal Expression of the 5HT3 Serotonin Receptor Gene Requires Nuclear Factor 1 Complexes
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[Abstract] [Full Text] [PDF]




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