Functional expression of influenza A viral nucleoprotein in cells transformed with cloned DNA.

Abstract:

:Simian cells permissive for influenza A virus infection were stably transformed with a full-length cloned influenza A nucleoprotein gene under the control of an inducible metallothionein promoter and linked to a dihydrofolate reductase gene to facilitate cell selection. Transformed cells synthesized a virus-specific nucleoprotein which was indistinguishable from the nucleoprotein synthesized in virus-infected cells with respect to molecular weight and intracellular localization. It was estimated that transformed cells produced only 1% of the amount of nucleoprotein synthesized in simian cells infected with influenza A virus. Nonetheless, when transformed cells were infected with influenza virus mutants which synthesized temperature-sensitive nucleoprotein, protein expressed by the cloned gene was able to complement the synthesis of plus-strand and minus-strand viral RNA for one mutant and only plus-strand synthesis for another mutant. This indicated that the influenza A nucleoprotein expressed in the transformed cells exhibited functional activity.

journal_name

Virology

journal_title

Virology

authors

Ryan KW,Mackow ER,Chanock RM,Lai CJ

doi

10.1016/0042-6822(86)90437-x

subject

Has Abstract

pub_date

1986-10-15 00:00:00

pages

144-54

issue

1

eissn

0042-6822

issn

1096-0341

journal_volume

154

pub_type

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