Berleth T, Nobis P, Jaenisch R, Harbers K
Heinrich-Pette-Institut für Experimentelle Virologie und Immunologie, Universität, Hamburg, F.R.G.
J Gen Virol. 1987 Nov;68 ( Pt 11):2919-23. doi: 10.1099/0022-1317-68-11-2919.
A collection of Mov mouse strains, each carrying in their germ line a Moloney murine leukaemia virus (M-MuLV) proviral genome at a different chromosomal location, was used to study expression of endogenous retroviruses. No M-MuLV-specific RNA was detected in the non-viraemic Mov strains studied, indicating that less than two copies of RNA are transcribed per cell. Virus expression was seen in three viraemic Mov strains. In Mov-3 mice the provirus was activated shortly after birth, whereas proviruses in Mov-9 and Mov-14 were activated at different stages of embryogenesis. The results suggest that the chromosomal position influences proviral expression during development. The first appearance of virus particles was not accompanied by detectable amounts of viral transcripts, suggesting that viraemia is a consequence of provirus activation in a small, as yet unidentified, population of cells, followed by virus spread and infection of susceptible cells.
利用一组Mov小鼠品系来研究内源性逆转录病毒的表达,每个品系在其种系中携带莫洛尼鼠白血病病毒(M-MuLV)前病毒基因组,且位于不同的染色体位置。在所研究的无病毒血症的Mov品系中未检测到M-MuLV特异性RNA,这表明每个细胞转录的RNA少于两份。在三个有病毒血症的Mov品系中观察到了病毒表达。在Mov-3小鼠中,出生后不久前病毒就被激活,而Mov-9和Mov-14中的前病毒在胚胎发育的不同阶段被激活。结果表明,染色体位置在发育过程中影响前病毒的表达。病毒颗粒的首次出现并未伴随着可检测到的病毒转录本,这表明病毒血症是一小群尚未确定的细胞中前病毒激活的结果,随后是病毒传播和对易感细胞的感染。