Gh. Reubel et Mj. Studdert, IDENTIFICATION, CLONING AND SEQUENCE-ANALYSIS OF THE EQUINE ADENOVIRUS-1 HEXON GENE, Archives of virology, 142(6), 1997, pp. 1193-1212
Based on sequence homology with human adenovirus 2 (HAdV2), the hexon
gene of equine adenovirus 1 (EAdV1) was identified. HindIII restrictio
n fragments containing the hexon and other viral genes were cloned int
o the plasmids pUC19 and pBlueScript SK(-) and sequenced. The nucleoti
de sequence of the hexon gene was completely determined and partial se
quence data were obtained for seven other EAdV1 genes. Amino acid (aa)
sequence comparison with published adenovirus (AdV) proteins identifi
ed the genes for the IIIa, penton, pVII, pVI, 23K proteinase, DNA bind
ing and 100K proteins. The eight EAdV1 genes appeared to be in the sam
e relative order as homologous genes of other AdV. The EAdV1 hexon pro
tein was encoded between the hexon-associated pVI upstream and the 23K
proteinase gene downstream and comprised 2742 nucleotides which trans
lated into 913 aa. Similar to other members of the genus Mastadenoviru
s the EAdV1 hexon yielded two highly conserved genome segments at the
N- and C-termini which flanked intermediate variable and hypervariable
regions. The majority of the residue differences between EAdV1 and ot
her AdV herons occurred in two loops that are known for other AdV to p
rotrude from the surface of the nucleocapsid. Amino acid comparisons w
ith other AdV herons revealed highest homology with HAdV12 hexon with
72% identical and 83% functionally similar residues, followed by bovin
e AdV3 hexon with 71% identities and 82% functional residue conservati
on. Phylogenetic analysis suggested that EAdV1 and other AdV do not ha
ve an immediate common ancestor.