Interaction of Bombyx mori nucleopolyhedrovirus BRO-A and host cell protein laminin
Article
Kang, WK, Imai, N, Suzuki, M et al. (2003). Interaction of Bombyx mori nucleopolyhedrovirus BRO-A and host cell protein laminin
. ARCHIVES OF VIROLOGY, 148(1), 99-113. 10.1007/s00705-002-0902-7
Kang, WK, Imai, N, Suzuki, M et al. (2003). Interaction of Bombyx mori nucleopolyhedrovirus BRO-A and host cell protein laminin
. ARCHIVES OF VIROLOGY, 148(1), 99-113. 10.1007/s00705-002-0902-7
The Bombyx mori nucleopolyhedrovirus (BmNPV) contains five baculovirus repeated ORF (bro) genes, all of which are expressed as delayed early genes. We have recently reported that BmNPV BRO proteins, specially BRO-A and BRO-C, contain a nucleic acid binding activity and are involved in nucleosome structures in nuclei of infected cells. To further understand the function of bro-a gene, we looked for factors interacting with BmNPV BRO-A using the yeast two-hybrid system. Fifteen clones obtained from a cDNA library of mock-infected cells and one from a library prepared at 2 h postinfection (p.i.) were found to comprise one distinct gene, which was identified as the Bombyx homolog (bLaminin) of Drosophila laminin β1. A direct interaction between BRO-A and N-terminal region of bLaminin was demonstrated by in vitro pull-down experiments. Further pull-down assays using BmN cell extracts and anti-laminin antibodies also showed interaction of both proteins. In addition, two more clones were obtained from cDNA library of 12 h p.i. and were found to encode BRO-A itself, indicating that BRO-A forms an oligomer. Taken together, we propose that BRO-A may function as a laminin binding protein.
