Mutational changes in the vesicular stomatitis virus glycoprotein affect the requirement of carbohydrate in

Journal of Virology
|January 1, 1981
PubMed

Insights

Simple mutations in vesicular stomatitis virus glycoprotein alter carbohydrate needs for virus formation. Some mutants, unlike wild-type virus, do not require glycosylation for efficient morphogenesis and particle release.

Area of Science:

  • Virology
  • Molecular Biology
  • Biochemistry

Background:

  • Vesicular stomatitis virus (VSV) morphogenesis is influenced by carbohydrate, with different strains exhibiting varying requirements.
  • Previous studies indicated strain-specific differences in VSV glycoprotein (G) glycosylation needs for cell surface migration and virion formation.

Purpose of the Study:

  • To investigate the role of carbohydrate in VSV morphogenesis.
  • To determine how specific mutations in the G protein affect its requirement for glycosylation.

Main Methods:

  • Utilized the antibiotic tunicamycin to inhibit glycosylation in VSV-infected cells.
  • Compared the morphogenesis and G protein behavior of wild-type VSV strains and various G protein mutants (tsO45, tsO44, tsO110, tsO44R) under different temperature and tunicamycin conditions.

Main Results:

  • Mutations within the G protein of the prototype VSV strain altered its carbohydrate requirement for morphogenesis at 30°C.
  • Mutants tsO45 and tsO44 showed no carbohydrate requirement, while tsO110 was completely dependent on glycosylation for G protein cell surface migration and particle release.
  • Wild-type VSV required carbohydrate at 39.5°C, but the tsO44R pseudorevertant eliminated this temperature-sensitive requirement, efficiently producing particles with unglycosylated G protein.

Conclusions:

  • Specific mutations in the VSV G protein can significantly alter or even eliminate its requirement for glycosylation during morphogenesis.
  • Simple mutational changes are sufficient to modify the carbohydrate dependency of viral glycoprotein processing and virion assembly.

Related Concept Videos

Viral Structure00:56

Viral Structure

Viruses are extraordinarily diverse in shape and size, but they all have several structural features in common. All viruses have a core that contains a DNA- or RNA-based genome. The core is surrounded by a protective coat of proteins called the capsid. The capsid is composed of subunits called capsomeres. The capsid and genome-containing core are together known as the nucleocapsid.
Viral Mutations00:36

Viral Mutations

A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material for adaptive...
Leaky Scanning02:28

Leaky Scanning

During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R stands for...
Overview of Secretory Vesicles01:33

Overview of Secretory Vesicles

Secretory vesicles, also known as dense core vesicles (DCVs), are membrane-bound vesicles that transport secretory proteins, such as hormones or neurotransmitters. Regulated secretory vesicles transport proteins from the trans-Golgi network to the exterior of the cell. Proteins present in regulated secretory vesicles are required to be rapidly exocytosed in large amounts upon a specific stimulus.
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
Coat Assembly and GTPases01:33

Coat Assembly and GTPases

Vesicles incorporate different coat protein subunits in different cell locations, which changes the properties of the coat, such as the shape and geometry of the transport vesicles. Thus, vesicle coat proteins also play a significant role in cargo selection.
Coat assembly depends on the local availability of phosphatidylinositol phosphates or PIPs and GTP-binding proteins. Adaptor proteins, which link the coat proteins to the membrane, bind to these PIPs and play a crucial role in controlling...
Inhibitors of Virion Maturation and Assembly01:19

Inhibitors of Virion Maturation and Assembly

As part of their replication cycle, certain viruses synthesize long precursor proteins called polyproteins within infected host cells. In human immunodeficiency virus (HIV), two major polyproteins are produced: Gag and Gag-Pol. The Gag polyprotein supplies the structural components of the virus, while Gag-Pol includes essential viral enzymes such as reverse transcriptase, integrase, and protease. After synthesis, these polyproteins move to the host cell membrane, where they assemble into an...