Juranek Stefan, Wieden Hans-Joachim, Lipps Hans J
Institute of Cell Biology, University Witten/Herdecke, Stockumer Strasse 10, D-58448 Witten, Germany.
Nucleic Acids Res. 2003 Mar 1;31(5):1387-91. doi: 10.1093/nar/gkg233.
Dramatic DNA reorganization and elimination processes occur during macronuclear differentiation in ciliates. In this study we analyzed whether cytosine methylation of specific sequences plays a functional role during DNA rearrangement. Three classes of sequences, macronuclear-destined sequences (MDSs, pCE7), members from a large family of transposon-like elements and micronuclear-specific sequences (pLJ01), differing in their structure and future destiny during nuclear differentiation, were studied in the micronucleus, the developing macronucleus and, when present, in the mature macronucleus. While the MDSs become processed to a 1.1 and 1.3 kb gene-sized macronuclear DNA molecule, the family of transposon-like elements represented by MaA81 becomes removed late in the course of polytene chromosome formation. The micronuclear-specific sequence pLJ01 is eliminated together with bulk micronuclear DNA during degradation of polytene chromosomes. No methylated cytosine could be detected in the vegetative macronucleus and no difference in methylation pattern was observed either between micronucleus and developing macronucleus in MDSs or in a micronuclear-specific sequence. However, a significant percentage of the cytosines contained in the transposon-like element becomes methylated de novo in the course of macronuclear differentiation. This is the first demonstration that cytosine methylation in specific sequences occurs during macronuclear differentiation and may provide a first step towards understanding epigenetic factors involved in DNA processing.
在纤毛虫的大核分化过程中会发生显著的DNA重组和消除过程。在本研究中,我们分析了特定序列的胞嘧啶甲基化在DNA重排过程中是否发挥功能作用。研究了三类序列,即注定进入大核的序列(MDSs,pCE7)、一个类似转座子元件的大家族的成员以及微核特异性序列(pLJ01),它们在核分化过程中的结构和未来命运各不相同,在微核、正在发育的大核以及(若存在)成熟大核中进行了研究。当MDSs被加工成1.1和1.3 kb基因大小的大核DNA分子时,以MaA81为代表的类似转座子元件家族在多线染色体形成过程后期被去除。微核特异性序列pLJ01在多线染色体降解过程中与大量微核DNA一起被消除。在营养大核中未检测到甲基化的胞嘧啶,在MDSs或微核特异性序列中,微核与正在发育的大核之间的甲基化模式也未观察到差异。然而,在大核分化过程中,类似转座子元件中所含的相当一部分胞嘧啶会重新发生甲基化。这是首次证明在大核分化过程中特定序列会发生胞嘧啶甲基化,并且可能为理解参与DNA加工的表观遗传因素迈出了第一步。