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Nucleotide sequence of the gene encoding the matrix protein of a recent measles virus isolate

M D Curran1, B K Rima

  • 1Department of Biology, Queen's University of Belfast, U.K.

Insights

The measles virus M gene sequence was determined for the Hu2 strain. Minor genetic changes were found compared to the Edmonston strain, impacting protein structure and potentially disease mechanisms.

Area of Science:

  • Virology
  • Molecular Biology
  • Genetics

Background:

  • Measles virus (MeV) causes a significant global health burden.
  • Understanding genetic variations in MeV strains is crucial for disease control and vaccine development.
  • The matrix (M) protein plays a key role in MeV assembly and pathogenesis.

Purpose of the Study:

  • To determine the complete nucleotide sequence of the M gene from the Hu2 strain of measles virus.
  • To compare the M gene sequence of the Hu2 strain with that of the Edmonston strain.
  • To analyze the implications of observed genetic variations on the M protein structure and function.

Main Methods:

  • Nucleotide sequencing of the M gene from the Hu2 measles virus strain.
  • Bioinformatic analysis to compare sequences with the Edmonston strain.
  • Analysis of nucleotide and amino acid substitutions.
  • Comparison with sequences from subacute sclerosing panencephalitis (SSPE) viruses.

Main Results:

  • Six nucleotide replacements were identified in the M gene's coding region compared to the Edmonston strain.
  • Two silent and four amino acid-altering substitutions were found, leading to a predicted Mr increase of 2000 for the M protein.
  • No changes were observed in the 5' untranslated region, but two changes occurred in the 3' untranslated region.
  • Sequence comparisons were made with published SSPE virus sequences.

Conclusions:

  • The Hu2 strain M gene exhibits specific genetic variations compared to the Edmonston strain.
  • These variations may influence M protein characteristics and potentially MeV pathogenesis.
  • Further research is needed to elucidate the functional impact of these M gene alterations in measles and SSPE.

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