Department of Microbiology and Immunology, Thomas Jefferson University, Philadelphia, PA USA.
Cell Cycle. 2011 Apr 1;10(7):1092-9. doi: 10.4161/cc.10.7.15089.
Colorectal cancer is a heterogeneous disease resulting from a combination of genetic and environmental factors. The C57BL/6J (B6) Apc (Min/+) mouse develops polyps throughout the gastrointestinal tract and has been a valuable model for understanding the genetic basis of intestinal tumorigenesis. Apc (Min/+) mice have been used to study known oncogenes and tumor suppressor genes on a controlled genetic background. These studies often utilize congenic knockout alleles, which can carry an unknown amount of residual donor DNA. The Apc (Min) model has also been used to identify modifer loci, known as Modifier of Min (Mom) loci, which alter Apc (Min) -mediated intestinal tumorigenesis. B6 mice carrying a knockout allele generated in WW6 embryonic stem cells were crossed to B6 Apc (Min/+) mice to determine the effect on polyp multiplicity. The newly generated colony developed significantly more intestinal polyps than Apc (Min/+) controls. Polyp multiplicity did not correlate with inheritance of the knockout allele, suggesting the presence of one or more modifier loci segregating in the colony. Genotyping of simple sequence length polymorphism (SSLP) markers revealed residual 129X1/SvJ genomic DNA within the congenic region of the parental knockout line. An analysis of polyp multiplicity data and SSLP genotyping indicated the presence of two Mom loci in the colony: 1) Mom12, a dominant modifier linked to the congenic region on chromosome 6, and 2) Mom13, which is unlinked to the congenic region and whose effect is masked by Mom12. The identification of Mom12 and Mom13 demonstrates the potential problems resulting from residual heterozygosity present in congenic lines.
结直肠癌是一种异质性疾病,由遗传和环境因素共同作用导致。C57BL/6J(B6)Apc(Min/+)小鼠在整个胃肠道中形成息肉,是研究肠道肿瘤发生遗传基础的重要模型。Apc(Min/+)小鼠已被用于在受控遗传背景下研究已知的癌基因和肿瘤抑制基因。这些研究通常利用同源敲除等位基因,这些等位基因可能带有未知量的残留供体 DNA。Apc(Min)模型还被用于鉴定修饰基因座,称为 Min 修饰基因座(Mom 基因座),这些基因座改变 Apc(Min)介导的肠道肿瘤发生。携带 WW6 胚胎干细胞中产生的敲除等位基因的 B6 小鼠与 B6 Apc(Min/+)小鼠杂交,以确定对息肉多发性的影响。新产生的品系比 Apc(Min/+)对照产生的肠道息肉多得多。息肉多发性与敲除等位基因的遗传无关,表明存在一个或多个在群体中分离的修饰基因座。简单序列长度多态性(SSLP)标记的基因分型显示,亲本敲除系的同源区域内存在残留的 129X1/SvJ 基因组 DNA。对息肉多发性数据和 SSLP 基因分型的分析表明,该群体中存在两个 Mom 基因座:1)Mom12,与染色体 6 上的同源区域连锁的显性修饰基因座;2)Mom13,与同源区域不连锁,其效应被 Mom12 掩盖。Mom12 和 Mom13 的鉴定表明,在同源系中存在残留杂合性会导致潜在问题。