Boone L R, Innes C L, Heitman C K
Cellular and Genetic Toxicology Branch, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709.
J Virol. 1990 Jul;64(7):3376-81. doi: 10.1128/JVI.64.7.3376-3381.1990.
The Fv-1b-mediated restriction of N-tropic retrovirus vector infection of BALB/3T3 cells was partially abrogated by prior infection with N-tropic murine leukemia virus. Likewise, abrogation of the Fv-1b restriction of N-tropic murine leukemia virus replication was accomplished by prior infection with genome-deficient virions produced by an N-tropic murine leukemia virus packaging cell line. The latter observation suggests that the Fv-1 target in genome-deficient virions abrogates Fv-1 restriction in the absence of any viral genome-directed processes.
用N-嗜性鼠白血病病毒预先感染可部分消除Fv-1b介导的对BALB/3T3细胞N-嗜性逆转录病毒载体感染的限制。同样,用N-嗜性鼠白血病病毒包装细胞系产生的基因组缺陷型病毒粒子预先感染,可消除Fv-1b对N-嗜性鼠白血病病毒复制的限制。后一观察结果表明,在没有任何病毒基因组导向过程的情况下,基因组缺陷型病毒粒子中的Fv-1靶点可消除Fv-1限制。