The 5' and 3' ends of the genome have a
cap and
poly(A) tract, respectively. The
viral envelope, obtained by budding through membranes of the
endoplasmic reticulum (ER) or
Golgi apparatus, invariably contains two virus-specified
glycoprotein species, known as the spike (S) and membrane (M) proteins. The
spike protein makes up the large surface projections (sometimes known as
peplomers), while the
membrane protein is a triple-spanning
transmembrane protein.
Toroviruses and a select subset of coronaviruses (in particular the members of subgroup A in the genus
Betacoronavirus) possess, in addition to the peplomers composed of S, a second type of surface projections composed of the
hemagglutinin-esterase protein. Another important structural
protein is the
phosphoprotein nucleocapsid protein (N), which is responsible for the helical symmetry of the nucleocapsid that encloses the genomic RNA. The fourth and smallest
viral structural protein is known as the
envelope protein (E), thought to be involved in
viral budding.
Genetic recombination can occur when at least two viral
genomes are present in the same infected host cell. RNA recombination appears to be a major driving force in coronavirus evolution. Recombination can determine genetic variability within a CoV species, the capability of a CoV species to jump from one host to another and, infrequently, the emergence of a novel CoV. The exact mechanism of recombination in CoVs is not known, but likely involves template switching during genome replication. ==Taxonomy==