B6.129S7-Gtrosa26 (B6.R26) mice carry a LacZ-neoR insertion on Chromosome (
Chr) 6, made by promoter trapping with 129 ES cells. Female C57BL/6J Apc(Mi
n)/+ (B6Min/+) mice are highly susceptible to intestinal tumors and to the
induction of mammary tumors after treatment with ethylnitrosourea (ENU). Ho
wever, B6.R26/+ Min/+ females develop fewer mammary and intestinal tumors a
fter ENU treatment than do B6 Min/+ mice. B6.R26/+ mice from two independen
tly derived congenic lines show this modifier effect. Each of these congeni
c lines carries approximately 20 cM of 129-derived DNA flanking the inserti
on, raising the possibility that the resistance is due to a linked modifier
locus. To further map the modifier locus, we have generated several lines
of mice carrying different regions of the congenic interval. We have found
that resistance to mammary and intestinal tumors in ENU-treated Min/+ mice
maps to a minimum 4-cM interval that includes the ROSA26 LacZ-neoR insertio
n. Therefore, the resistance to tumor development is due to either the ROSA
26 insertion or a very tightly linked modifier locus.