Jönsson F, Wen J P, Fetzer C P, Lipps H J
Institut für Zellbiologie, Universität Witten/Herdecke, D-58448 Witten, Germany.
Nucleic Acids Res. 1999 Jul 15;27(14):2832-41. doi: 10.1093/nar/27.14.2832.
During macronuclear differentiation in ciliated protozoa a series of programed DNA reorganization processes occur. These include the elimination of micronuclear-specific DNA sequences, the specific fragmentation of the genome into small gene-sized DNA molecules, the de novo addition of telomeric sequences to these DNA molecules and the specific amplification of the remaining DNA molecules. Recently we constructed a vector containing the modified micronuclear version of macronuclear destined DNA sequences that was correctly fragmented and telomeres were added de novo after injection into the developing macronucleus. It therefore must contain all the cis- acting sequences required for these processes. We made a series of vectors deleting different sequences from the original vector. It could be shown that at least in the case studied here no micronuclear-specific sequences are required for specific fragmentation of the genome and telomere addition. However, a short subtelomeric sequence at the 3[prime]-end is essential for these processes, whereas no specific cut seems to occur at the 5[prime]-end. In addition, we can show that the processing activity is restricted to a short period of time during macronuclear differentiation and that a preceding transcription is required for correct processing of macronuclear-destined DNA sequences. Possible mechanisms of these processes will be discussed.
在纤毛原生动物的大核分化过程中,会发生一系列程序性DNA重组过程。这些过程包括微核特异性DNA序列的消除、基因组特异性断裂成小的基因大小的DNA分子、端粒序列从头添加到这些DNA分子以及剩余DNA分子的特异性扩增。最近,我们构建了一个载体,其中包含注定要进入大核的DNA序列的修饰微核版本,该载体在注入发育中的大核后能正确断裂并从头添加端粒。因此,它一定包含这些过程所需的所有顺式作用序列。我们制作了一系列从原始载体中删除不同序列的载体。可以证明,至少在这里研究的案例中,基因组的特异性断裂和端粒添加不需要微核特异性序列。然而,3′端的一个短的亚端粒序列对这些过程至关重要,而5′端似乎没有特异性切割。此外,我们可以表明,加工活性在大核分化过程中仅限于一段短时间,并且注定要进入大核的DNA序列的正确加工需要先前的转录。将讨论这些过程的可能机制。