Yu Ying, Zhang Huanmin, Tian Fei, Zhang Wensheng, Fang Hongbin, Song Jiuzhou
Department of Animal and Avian Sciences, University of Maryland, College Park, Maryland, United State of America.
PLoS One. 2008 Jul 16;3(7):e2672. doi: 10.1371/journal.pone.0002672.
Both epigenetic alterations and genetic variations play essential roles in tumorigenesis. The epigenetic modification of DNA methylation is catalyzed and maintained by the DNA methyltransferases (DNMT3a, DNMT3b and DNMT1). DNA mutations and DNA methylation profiles of DNMTs themselves and their relationships with chicken neoplastic disease resistance and susceptibility are not yet defined. In the present study, we analyzed the complexity of the DNA methylation variations and DNA mutations in the first exon of three DNMTs genes over generations, tissues, and ages among chickens of two highly inbred White Leghorn lines, Marek's disease-resistant line 6(3) and -susceptible line 7(2), and six recombinant congenic strains (RCSs). Among them, tissue-specific methylation patterns of DNMT3a were disclosed in spleen, liver, and hypothalamus in lines 6(3) and 7(2). The methylation level of DNMT3b on four CpG sites was not significantly different among four tissues of the two lines. However, two line-specific DNA transition mutations, CpG-->TpG (Chr20:10203733 and 10203778), were discovered in line 7(2) compared to the line 6(3) and RCSs. The methylation contents of DNMT1 in blood cell showed significant epimutations in the first CpG site among the two inbred lines and the six RCSs (P<0.05). Age-specific methylation of DNMT1 was detected in comparisons between 15 month-old and 2 month-old chickens in both lines except in spleen samples from line 7(2). No DNA mutations were discovered on the studied regions of DNMT1 and DNMT3a among the two lines and the six RCSs. Moreover, we developed a novel method that can effectively test the significance of DNA methylation patterns consisting of continuous CpG sites. Taken together, these results highlight the potential of epigenetic alterations in DNMT1 and DNMT3a, as well as the DNA mutations in DNMT3b, as epigenetic and genetic factors to neoplastic diseases of chickens.
表观遗传改变和基因变异在肿瘤发生过程中都起着至关重要的作用。DNA甲基化的表观遗传修饰由DNA甲基转移酶(DNMT3a、DNMT3b和DNMT1)催化并维持。DNMTs自身的DNA突变和DNA甲基化谱及其与鸡肿瘤疾病抗性和易感性的关系尚未明确。在本研究中,我们分析了两个高度近交的白来航鸡品系(马立克氏病抗性品系6(3)和易感品系7(2))以及六个重组近交系(RCSs)中,三个DNMTs基因第一外显子在代际、组织和年龄方面的DNA甲基化变异和DNA突变的复杂性。其中,在品系6(3)和7(2)的脾脏、肝脏和下丘脑中揭示了DNMT3a的组织特异性甲基化模式。两个品系的四个组织中,DNMT3b在四个CpG位点的甲基化水平无显著差异。然而,与品系6(3)和RCSs相比,在品系7(2)中发现了两个品系特异性的DNA转换突变,即CpG→TpG(Chr20:10203733和10203778)。血细胞中DNMT1的甲基化含量在两个近交系和六个RCSs的第一个CpG位点显示出显著的表观突变(P<0.05)。除了品系7(2)的脾脏样本外,在两个品系中15月龄和2月龄鸡的比较中检测到了DNMT1的年龄特异性甲基化。在两个品系和六个RCSs中,未在DNMT1和DNMT3a的研究区域发现DNA突变。此外,我们开发了一种新方法,可有效检验由连续CpG位点组成的DNA甲基化模式的显著性。综上所述,这些结果突出了DNMT1和DNMT3a表观遗传改变以及DNMT3b中DNA突变作为鸡肿瘤疾病的表观遗传和遗传因素的潜力。