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首页> 外文期刊>Journal of Virology >Complementation of adenovirus type 5 host range mutants by adenovirus type 12 in coinfected HeLa and BHK-21 cells.
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Complementation of adenovirus type 5 host range mutants by adenovirus type 12 in coinfected HeLa and BHK-21 cells.

机译:腺病毒12型腺病毒型12型腺瘤型12在辛的HeLa和BHK-21细胞中的互补型均突变体。

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We have studied the ability of adenovirus type 12 (Ad12) to complement the Ad5 transformation-defective host rang (hr) mutants during infection of human cells (HeLa) or hamster cells (BHK-21). The group I mutant hr3 (mapped within 1.3 to 3.7 map units), which is incapable of synthesizing viral DNA, was complemented for both DNA synthesis and infectious virus production in nonpermissive HeLa cells during coinfection with Ad12. Similarly, the group II mutant hr6 (6.1 to 9.4 map units), which does synthesize DNA, was also shown to be complemented for virus production. When the host cells were BHK-21, an established hamster cell line that is permissive for Ad5 but nonpermissive for Ad12 DNA synthesis and virus production, coinfection with Ad5 and Ad12 did not overcome the block to Ad12 DNA synthesis. Coinfection of BHK-21 cells with Ad12 and either hr3 or hr6 leads to the complementation of only the group I mutant (hr3). The inability of Ad12 to complement hr6 in BHK-21 cells may be due to the failure of Ad12 to express an early gene product from the region corresponding to early region 1B (4.5 to 11 map units) Ad5 where hr6 and the other group II mutations are located.
机译:我们研究了腺病毒型12(AD12)的能力在感染人体细胞(HELA)或仓鼠细胞(BHK-21)感染期间补充AD5转化缺陷宿主rang(HR)突变体。 I族突变体HR3(映射到1.3至3.7内的地图单元中),其无法合成病毒DNA,在与AD12的繁殖期间,在非智能HeLa细胞中的DNA合成和传染性病毒产生辅成。类似地,还显示合成DNA的II族突变体HR6(6.1至9.4个地图单元),用于病毒产生补充。当宿主细胞为BHK-21时,允许AD5的允许但对于AD12 DNA合成和病毒产生的非施用,与AD5和AD12的杂交,没有克服该嵌段对AD12 DNA合成的植物进行杂散但不令人生动的仓鼠细胞系。使用Ad12和HR3或HR6的BHK-21细胞的繁殖导致仅I基团突变体(HR3)的互补。在BHK-21细胞中的AD12在BHK-21细胞中的不稳定可以是由于AD12的发生故障,以从对应于对应于早期区域1B(4.5至11个MAP单元)AD5的区域的早期基因产物,其中HR6和其他II族突变位于。

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