Recombinations between c-myc and immunoglobulin (Ig) sequences that ty
pically occur in pristane-induced mouse plasmacytomas were detected in
secondary lymphoid tissues from normal mice, chiefly in the gut-assoc
iated lymphoid tissue. Based on the analysis of recombination sequence
s as clonotypic markers, migration of c-myc recombination-positive cel
ls was observed between Peyer's patches and into the intestine. Treatm
ent of plasmacytoma-susceptible BALB/cAn mice with pristane induced pr
oliferation and migration of these cells into mesenteric lymph node, s
pleen, and oil granuloma within 7 days. Plasmacytoma-resistant strains
of mice (DBA/2N, C3H/HeJ, C57BL/6) differed in that (1) they harbored
fewer clones (Ig/c-myc recombinations were detected in 33% of resista
nt mice versus 91% of BALB/cAn mice after pristane treatment); (2) Ig/
c-myc-positive cells were rarely detected in the oil granuloma, and (3
) c-myc recombined predominantly with the Ig alpha locus in BALB/cAn m
ice (72%), but with the Ig mu locus in DBA/2N and in C57BL/6 (67%). Th
e results demonstrate that normal mice generate a large number of lymp
hocytes with aberrant c-myc in intestinal tissues without developing t
umors.