Lawton Betty R, Carone Benjamin R, Obergfell Craig J, Ferreri Gianni C, Gondolphi Christina M, Vandeberg John L, Imumorin Ikhide, O'Neill Rachel J, O'Neill Michael J
Department of Molecular and Cell Biology, University of Connecticut, 354 Mansfield Rd., Storrs, CT 06269, USA .
BMC Genomics. 2008 May 2;9:205. doi: 10.1186/1471-2164-9-205.
Parent-specific methylation of specific CpG residues is critical to imprinting in eutherian mammals, but its importance to imprinting in marsupials and, thus, the evolutionary origins of the imprinting mechanism have been the subject of controversy. This has been particularly true for the imprinted Insulin-like Growth Factor II (IGF2), a key regulator of embryonic growth in vertebrates and a focal point of the selective forces leading to genomic imprinting. The presence of the essential imprinting effector, DNMT3L, in marsupial genomes and the demonstration of a differentially methylated region (DMR) in the retrotransposon-derived imprinted gene, PEG10, in tammar wallaby argue for a role for methylation in imprinting, but several studies have found no evidence of parent-specific methylation at other imprinted loci in marsupials.
We performed the most extensive search to date for allele-specific patterns of CpG methylation within CpG isochores or CpG enriched segments across a 22 kilobase region surrounding the IGF2 gene in the South American opossum Monodelphis domestica. We identified a previously unknown 5'-untranslated exon for opossum IGF2, which is flanked by sequences defining a putative neonatal promoter, a DMR and an active Matrix Attachment Region (MAR). Demethylation of this DMR in opossum neonatal fibroblasts results in abherrant biallelic expression of IGF2.
The demonstration of a DMR and an active MAR in the 5' flank of opossum IGF2 mirrors the regulatory features of the 5' flank of Igf2 in mice. However, demethylation induced activation of the maternal allele of IGF2 in opossum differs from the demethylation induced repression of the paternal Igf2 allele in mice. While it can now be concluded that parent-specific DNA methylation is an epigentic mark common to Marsupialia and Eutheria, the molecular mechanisms of transcriptional silencing at imprinted loci have clearly evolved along independent trajectories.
特定CpG残基的亲本特异性甲基化对于真兽亚纲哺乳动物的印记形成至关重要,但其对有袋类动物印记形成的重要性以及印记机制的进化起源一直存在争议。对于印记基因胰岛素样生长因子II(IGF2)而言尤其如此,IGF2是脊椎动物胚胎生长的关键调节因子,也是导致基因组印记的选择力的焦点。有袋类动物基因组中存在必需的印记效应因子DNMT3L,并且在袋鼩的反转录转座子衍生的印记基因PEG10中发现了差异甲基化区域(DMR),这表明甲基化在印记形成中发挥作用,但多项研究未在有袋类动物的其他印记位点发现亲本特异性甲基化的证据。
我们对南美负鼠短尾负鼠围绕IGF2基因的22千碱基区域内的CpG同线序列或富含CpG的片段中的CpG甲基化等位基因特异性模式进行了迄今为止最广泛的搜索。我们鉴定出了负鼠IGF2一个先前未知的5'-非翻译外显子,其两侧是定义推定的新生启动子、一个DMR和一个活性基质附着区域(MAR)的序列。负鼠新生成纤维细胞中该DMR的去甲基化导致IGF2异常的双等位基因表达。
负鼠IGF2 5'侧翼区存在DMR和活性MAR反映了小鼠Igf2 5'侧翼区的调控特征。然而,负鼠中去甲基化诱导的IGF2母本等位基因激活不同于小鼠中去甲基化诱导的父本Igf2等位基因抑制。虽然现在可以得出结论,亲本特异性DNA甲基化是有袋类动物和真兽亚纲动物共有的表观遗传标记,但印记位点转录沉默的分子机制显然是沿着独立的轨迹进化的。