Three mRNAs from the murine polyomavirus early region encode the three
well-characterized tumor antigens, We report the existence of a fourt
h alternatively spliced mRNA which encodes a fourth tumor antigen, tin
y T antigen, which comprises the amino-terminal domain common to all o
f the T antigens but is extended by six unique amino acid residues, Th
e amount of tiny T antigen in infected cells is small because of its s
hort half-life. Tiny T antigen stimulates the ATPase activity of Hsc70
, most likely because of its DnaJ-like motif, The common amino-termina
l domain may interface with chaperone complexes to assist the T antige
ns in carrying out their diverse functions of replication, transcripti
on, and transformation in the appropriate cellular compartments.