Comparative structural analysis of transcriptionally competent and incompetent rotavirus-antibody complexes

Citation
Ja. Lawton et al., Comparative structural analysis of transcriptionally competent and incompetent rotavirus-antibody complexes, P NAS US, 96(10), 1999, pp. 5428-5433
Citations number
29
Categorie Soggetti
Multidisciplinary
Journal title
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
ISSN journal
00278424 → ACNP
Volume
96
Issue
10
Year of publication
1999
Pages
5428 - 5433
Database
ISI
SICI code
0027-8424(19990511)96:10<5428:CSAOTC>2.0.ZU;2-G
Abstract
During genome transcription in rotavirus, as with many segmented double-str anded RNA viruses, mRNA is transcribed within the intact subviral particle and translocated through specific channels in the capsid, To understand how the conformation of the capsid affects the efficiency of transcriptional e vents in the viral core, we carried out a series of comparative structural and biochemical studies to characterize four different structural forms of the virus exhibiting differing transcriptional behavior. Two of these were virus-antibody complexes having contrasting transcriptional capabilities, a nd two were variant structural forms of the virus that exist during the lif e cycle and also exhibit contrasting transcriptional behavior. Three-dimens ional structural studies using electron cryomicroscopy showed that the bind ing of one Fab (8H2/G5) does not affect the conformation of the capsid, and the efficiency of mRNA production is similar to that of the native subvira l particle. The other Fab (2A11/E9) introduces conformational changes in th e capsid similar to those seen in the transcriptionally incompetent mature particle. In both of the transcriptionally incompetent particle types, mRNA synthesis was arrested after limited elongation with the resulting oligonu cleotide transcripts remaining trapped inside the particles. Our results in dicate that the continuous translocation of nascent mRNA through the capsid is critical for efficient transcript elongation and that the blockage of t ranslocation causes premature termination of transcription.