| Literature DB >> 17416904 |
Daisuke Shiokawa1, Tokiyoshi Matsushita, Yukari Shika, Mamoru Shimizu, Masahiro Maeda, Sei-ichi Tanuma.
Abstract
DNase X is the first mammalian DNase to be isolated that is homologous to DNase I. In this study, we have examined its function using a novel monoclonal antibody and showed it to be expressed on the cell surface as a glycosylphosphatidylinositolanchored membrane protein. High level expression was observed in human muscular tissues and in myotubes obtained in vitro from RD rhabdomyosarcoma cells. We observed that RD myotubes incorporated a foreign gene, lacZ, by endocytosis but that expression of the encoded coding product, beta-galactosidase, was strongly inhibited. Overexpression of DNase X inhibited endocytosis-mediated gene transfer, whereas knockdown of DNase X with small interfering RNA had the opposite effect. These results reveal that DNase X provides a cell surface barrier to endocytosis-mediated gene transfer.Entities:
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Year: 2007 PMID: 17416904 DOI: 10.1074/jbc.M610428200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157