Reovirus Type 3 Genome Segment S4: Nucleotide Sequence of the Gene Encoding a Major Virion Surface Protein

1985 ◽  
Vol 53 (2) ◽  
pp. 710-710
Keyword(s):  
Nucleotide Sequence ◽  
Surface Protein ◽  
Genome Segment ◽  
Gene Encoding ◽  
Reovirus Type ◽  
Type 3 ◽  
Virion Surface

scholarly journals Sites and Determinants of Early Cleavages in the Proteolytic Processing Pathway of Reovirus Surface Protein σ3

2002 ◽  
Vol 76 (10) ◽  
pp. 5184-5197 ◽  
Author(s):  
Judit Jané-Valbuena ◽  
Laura A. Breun ◽  
Leslie A. Schiff ◽  
Max L. Nibert
Keyword(s):  
Structural Changes ◽  
Proper Time ◽  
Strain Differences ◽  
Surface Protein ◽  
Cellular Membrane ◽  
Proteolytic Processing ◽  
Target Cells ◽  
Inactive Form ◽  
Reovirus Type ◽  
Type 3

ABSTRACT Entry of mammalian reovirus virions into target cells requires proteolytic processing of surface protein σ3. In the virion, σ3 mostly covers the membrane-penetration protein μ1, appearing to keep it in an inactive form and to prevent it from interacting with the cellular membrane until the proper time in infection. The molecular mechanism by which σ3 maintains μ1 in this inactive state and the structural changes that accompany σ3 processing and μ1 activation, however, are not well understood. In this study we characterized the early steps in σ3 processing and determined their effects on μ1 function and particle infectivity. We identified two regions of high protease sensitivity, “hypersensitive” regions located at residues 208 to 214 and 238 to 244, within which all proteases tested selectively cleaved σ3 as an early step in processing. Further processing of σ3 was required for infection, consistent with the fact that the fragments resulting from these early cleavages remained bound to the particles. Reovirus type 1 Lang (T1L), type 3 Dearing (T3D), and T1L × T3D reassortant virions differed in the sites of early σ3 cleavage, with T1L σ3 being cleaved mainly at residues 238 to 244 and T3D σ3 being cleaved mainly at residues 208 to 214. These virions also differed in the rates at which the early cleavages occurred, with cleavage of T1L σ3 occurring faster than cleavage of T3D σ3. Analyses using chimeric and site-directed mutants of recombinant σ3 identified carboxy-proximal residues 344, 347, and 353 as the primary determinants of these strain differences. The spatial relationships between these more carboxy-proximal residues and the hypersensitive regions were discerned from the σ3 crystal structure. The results indicate that proteolytic processing of σ3 during reovirus disassembly is a multistep pathway with a number of molecular determinants.

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