Kohlhepp R L, Hegge L F, Moser A R
The Department of Human Oncology, K4/330 CSC 3864, 600 Highland Ave, University of Wisconsin-Madison, Madison, Wisconsin 53792, USA.
Mamm Genome. 2001 Aug;12(8):606-11. doi: 10.1007/s003350020042.
B6.129S7-Gtrosa26 (ROSA26) mice carry a LacZ-neo(R) insertion on Chromosome (Chr) 6, made by promoter trapping with AB1 129 ES cells. Female C57BL/6J Apc(Min/+) (B6 Min/+) mice are very susceptible to the induction of mammary tumors after treatment with ethylnitrosourea (ENU). However, ENU-treated B6 mice carrying both Apc(Min) and ROSA26 are resistant to mammary tumor formation. Thus, ROSA26 mice carry a modifier of Min-induced mammary tumor susceptibility. We have previously mapped the modifier to a 4-cM interval of 129-derived DNA that also contains the ROSA26 insertion. Here we report additional evidence for the effect of the ROSA26 insertion on mammary tumor formation. To test the hypothesis that the resistance was due to a linked modifier locus, we utilized two approaches. We have derived and tested two lines of mice that are congenic for 129-derived DNA within the minimal modifier interval and show that they are as susceptible to mammary tumors as are B6 mice. Additionally, we analyzed a backcross population segregating for the insertion and show that mice carrying the insertion are more resistant to mammary tumor development than are mice not carrying the insertion. Thus, the resistance is not due to a 129-derived modifier allele, but must be due to the ROSA26 insertion. In addition, the effect of the ROSA26 insertion can be detected in a backcross population segregating for other mammary modifiers.
B6.129S7-Gtrosa26(ROSA26)小鼠在6号染色体(Chr)上携带LacZ-新霉素抗性基因(neo)插入片段,该插入是通过用AB1 129胚胎干细胞进行启动子捕获实现的。雌性C57BL/6J Apc(Min/+)(B6 Min/+)小鼠在用乙基亚硝基脲(ENU)处理后极易诱发乳腺肿瘤。然而,同时携带Apc(Min)和ROSA26的ENU处理的B6小鼠对乳腺肿瘤形成具有抗性。因此,ROSA26小鼠携带一种修饰基因,可调节Min诱导的乳腺肿瘤易感性。我们之前已将该修饰基因定位到一段129来源的DNA的4厘摩区间,该区间也包含ROSA26插入片段。在此,我们报告关于ROSA26插入对乳腺肿瘤形成影响的更多证据。为了检验抗性是由于一个连锁修饰基因座这一假说,我们采用了两种方法。我们培育并检测了两系小鼠,它们在最小修饰区间内对于129来源的DNA是同源的,结果显示它们与B6小鼠一样易患乳腺肿瘤。此外,我们分析了一个针对该插入片段进行分离的回交群体,结果表明携带该插入片段的小鼠比未携带该插入片段的小鼠对乳腺肿瘤发展更具抗性。因此,抗性并非由于129来源的修饰等位基因,而必定是由于ROSA26插入片段。此外,在针对其他乳腺修饰基因进行分离的回交群体中也能检测到ROSA26插入片段的影响。