Jaraczewski J W, Frels J S, Jahn C L
Department of Cell and Molecular Biology, Northwestern University Medical School, Chicago, IL 60611.
Nucleic Acids Res. 1994 Oct 25;22(21):4535-42. doi: 10.1093/nar/22.21.4535.
During macromolecular development in the ciliated protozoan, Euplotes crassus, > 105 Tec elements are precisely eliminated from the genome in a 2-4 h time interval, generating extrachromosomal circular forms of the elements. Various models have proposed a transposition-based mechanism for this excision. We have tested this hypothesis by determining the abundance of transcripts of Tec element open reading frames (ORFs) and the timing of their appearance. Transcripts are very low in abundance and are only detected by PCR amplification techniques. Thus, the low levels of transcripts argue against the participation of element-encoded functions in the Tec element elimination process. The element transcripts are only detected in RNA samples from mated cells, indicating that the micronucleus and/or developing macronucleus are transcriptionally active during the sexual phase of the life cycle. The transcription detected could allow a low level of germline-specific transposition for these elements.
在纤毛原生动物粗多毛虫的大分子发育过程中,超过105个Tec元件在2 - 4小时的时间间隔内从基因组中精确消除,产生该元件的染色体外环状形式。各种模型提出了一种基于转座的切除机制。我们通过确定Tec元件开放阅读框(ORF)转录本的丰度及其出现时间来检验这一假设。转录本丰度非常低,仅通过PCR扩增技术才能检测到。因此,转录本水平低表明元件编码的功能不参与Tec元件消除过程。元件转录本仅在来自交配细胞的RNA样本中检测到,这表明小核和/或发育中的大核在生命周期的有性阶段具有转录活性。检测到的转录可能允许这些元件进行低水平的种系特异性转座。