Laboratory of Anatomy, Department of Biomedical Sciences, Graduate School of Veterinary Medicine, Hokkaido University, Kita 18-Nishi 9, Kita-ku, Sapporo, 060-0818, Japan.
Mamm Genome. 2010 Apr;21(3-4):162-71. doi: 10.1007/s00335-010-9254-x. Epub 2010 Feb 25.
MRL/MpJ (MRL) is a model mouse for autoimmune diseases such as dermatitis, vasculitis, arthritis, and glomerulonephritis. In addition to these immune-associated disorders, we found that older MRL mice develop ovarian cysts originating from the rete ovarii, which is lined by ciliated or nonciliated epithelium and considered remnants of mesonephric tubules. Ovarian cysts, which are reported to have several sources, are associated with female infertility, but information regarding the genetic etiology of ovarian cysts originating from the rete ovarii is rare. In this study, to elucidate the genetic background of development of ovarian cysts, we performed quantitative trait locus (QTL) analysis using 120 microsatellite markers, which cover the whole genome of murine chromosomes, and 213 backcross progenies between female MRL and male C57BL/6N mice. The quantitative trait measured was the circumferences of rete ovarii or ovarian cysts. As a result, suggestive linkages were detected on Chrs 3, 4, 6, and 11, but significant linkages were located on Chr 14 by interval mapping. We thereby designated the 27.5-cM region of Chr 14 "MRL Rete Ovarian Cysts (mroc)." The peak regions of Chrs 4 and 14 in particular showed a close additive interaction (p < 0.00001). From these results we concluded that multiple loci on Chrs 3, 4, 6, 11, and 14 interact to result in development of ovarian cysts in MRL mice.
MRL/MpJ(MRL)是一种自身免疫性疾病的模型鼠,例如皮炎、血管炎、关节炎和肾小球肾炎。除了这些免疫相关疾病外,我们发现老年 MRL 小鼠会出现起源于卵巢网的卵巢囊肿,卵巢网由纤毛或非纤毛上皮细胞衬里,被认为是中肾管的残余物。卵巢囊肿有多种来源,与女性不孕有关,但关于起源于卵巢网的卵巢囊肿的遗传病因的信息很少。在这项研究中,为了阐明卵巢囊肿发生的遗传背景,我们使用覆盖鼠染色体全基因组的 120 个微卫星标记和雌性 MRL 和雄性 C57BL/6N 小鼠之间的 213 个回交后代进行了数量性状基因座(QTL)分析。测量的数量性状是卵巢网或卵巢囊肿的周长。结果,在 Chrs 3、4、6 和 11 上检测到了暗示性的连锁,但通过区间作图在 Chr 14 上检测到了显著的连锁。因此,我们将 Chr 14 的 27.5-cM 区域命名为“MRL 卵巢网囊肿(mroc)”。特别是 Chrs 4 和 14 的峰值区域表现出密切的累加交互作用(p <0.00001)。根据这些结果,我们得出结论,Chrs 3、4、6、11 和 14 上的多个位点相互作用导致 MRL 小鼠中卵巢囊肿的发展。