Paulsen M, Takada S, Youngson N A, Benchaib M, Charlier C, Segers K, Georges M, Ferguson-Smith A C
University of Cambridge, Department of Anatomy, Cambridge CB2 3DY, United Kingdom.
Genome Res. 2001 Dec;11(12):2085-94. doi: 10.1101/gr.206901.
The Dlk1-Gtl2 domain on mouse chromosome 12 contains reciprocally imprinted genes with the potential to contribute to our understanding of common features involved in imprinting control. We have sequenced this conserved region in the mouse and sheep and included the human sequence in a three species comparison. This analysis resulted in a precise conservation map and identification of highly conserved sequence elements, some of which we have shown previously to be differentially methylated in the mouse. Additionally, this analysis facilitated identification of a CpG-rich tandem repeat array located approximately 13-15 kb upstream of Gtl2. Furthermore, we have identified a third imprinted transcript that overlaps with the last Dlk1 exon in the mouse. This transcript lacks a conserved open reading frame and is probably generated by cleavage of extended Dlk1 transcripts. Because Dlk1 and Gtl2 share many of the imprinting properties of the well-characterized Igf2-H19 domain, it has been proposed that the two regions may be regulated in the same way. Comparative genomic examination of the two domains indicates that although there are similarities, other features are very different, including the location of conserved CTCF-binding sites, and the level of conservation at regulatory regions.
小鼠12号染色体上的Dlk1-Gtl2区域包含相互印记的基因,这些基因有助于我们理解印记控制中涉及的共同特征。我们已对小鼠和绵羊的这一保守区域进行了测序,并将人类序列纳入了三物种比较中。该分析产生了一个精确的保守图谱,并鉴定出了高度保守的序列元件,其中一些我们之前已证明在小鼠中存在差异甲基化。此外,该分析有助于鉴定位于Gtl2上游约13 - 15 kb处的富含CpG的串联重复序列阵列。此外,我们还鉴定出了第三种印记转录本,它与小鼠中Dlk1的最后一个外显子重叠。该转录本缺乏保守的开放阅读框,可能是由延长的Dlk1转录本的切割产生的。由于Dlk1和Gtl2具有许多已充分表征的Igf2-H19区域的印记特性,因此有人提出这两个区域可能以相同的方式受到调控。对这两个区域的比较基因组研究表明,尽管存在相似之处,但其他特征却非常不同,包括保守的CTCF结合位点的位置以及调控区域的保守程度。