Hostname: page-component-848d4c4894-m9kch Total loading time: 0 Render date: 2024-06-08T06:04:41.886Z Has data issue: false hasContentIssue false

Towards Understanding the Structural Requirements for Endogenous Transcription in Rotavirus

Published online by Cambridge University Press:  02 July 2020

J. A. Lawton
Affiliation:
Program in Cell and Molecular Biology, Houston, TX77030.
M. K. Estes
Affiliation:
Division of Molecular Virology, Baylor College of Medicine, Houston, TX77030.
B. V. Venkataram Prasad
Affiliation:
Department of Biochemistry, Houston, TX77030.
Get access

Extract

Rotaviruses are complex, relatively large (1000 Å) nonenveloped icosahedral viruses. They are the major causative agents of severe diarrhea in children and animals. Annually an estimated 1 million children die from rotavirus-induced gastroenteritis worldwide. Medical relevance, intriguing structural complexity, and several unique strategies in the morphogenesis and replication have provoked extensive molecular biological and structural studies on rotaviruses in recent years.

Rotaviruses are double-stranded RNA (dsRNA) viruses belonging to the family Reoviridae. Each of the 11 segments codes for one protein. Of the eleven proteins encoded by the genomic RNA, six are structural and five are non-structural. Structural studies have shown that mature rotaviruses are triple-layered particles (TLPs). During the process of cell entry the outer-most layer consisting of VP7 and the spike protein VP4 is lost and the resulting double layered particles (DLPs) become transcriptionally active (Fig. 1 A). During the process of transcription, the DLPs maintain their structural Integrity.

Type
Application of Classical and Novel Microscopy to Tissue Injury and Infectious Disease Pathogenesis
Copyright
Copyright © Microscopy Society of America

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Prasad, B.V.V. and Estes, M.K., in Chiu et al., Eds., Structural Biology of Viruses, New York: Oxford (1996) 239.Google Scholar

2. Prasad, B.V.V. et al., Nature 382 (1996)471.CrossRefGoogle Scholar

3. Lawton, J. A. et al., Nature Struct. Biol. 4 (1977)118.CrossRefGoogle Scholar

4. We acknowledge Dr. Richard Ward for a generous gift of anti-VP6 ascites, and support from NIH grants Al 36040 (BVVP), DK 30144 (MKE), and a training fellowship to JAL (GM-08280).Google Scholar