DuBois M, Prescott D M
Department of Molecular, Cellular and Development Biology, University of Colorado, Boulder 80309-0347, USA.
Proc Natl Acad Sci U S A. 1995 Apr 25;92(9):3888-92. doi: 10.1073/pnas.92.9.3888.
The DNA in a germ-line nucleus (a micronucleus) undergoes extensive processing when it develops into a somatic nucleus (a macronucleus) after cell mating in hypotrichous ciliates. Processing includes destruction of a large amount of spacer DNA between genes and excision of gene-sized molecules from chromosomes. Before processing, micronuclear genes are interrupted by numerous noncoding segments called internal eliminated sequences (IESs). The IESs are excised and destroyed, and the retained macro-nuclear-destined sequences (MDSs) are spliced. MDSs in some micronuclear genes are not in proper order and must be reordered during processing to create functional gene-sized molecules for the macronucleus. Here we report that the micronuclear actin I gene in Oxytricha trifallax WR consists of 10 MDSs and 9 IESs compared to the previously reported 9 MDSs and 8 IESs in the micronuclear actin I gene of Oxytricha nova. The MDSs in the actin I gene are scrambled in a similar pattern in the two species, but the positions of MDS-IES junctions are shifted by up to 14 bp for scrambled and 138 bp for the nonscrambled MDSs. The shifts in MDS-IES junctions create differences in the repeat sequences that are believed to guide MDS splicing. Also, the sizes and sequences of IESs in the micronuclear actin I genes are different in the two Oxytricha species. These observations give insight about the possible origins of IES insertion and MDS scrambling in evolution and show the extraordinary malleability of the germ-line DNA in hypotrichs.
在寡毛纲纤毛虫细胞交配后,生殖细胞核(微核)中的DNA在发育成体细胞核(大核)时会经历广泛的加工过程。加工过程包括破坏基因之间大量的间隔DNA以及从染色体上切除基因大小的分子。在加工之前,微核基因被许多称为内部消除序列(IESs)的非编码片段打断。IESs被切除并破坏,保留的大核定向序列(MDSs)被拼接起来。一些微核基因中的MDSs顺序不正确,在加工过程中必须重新排序,以产生用于大核的功能性基因大小的分子。在这里我们报告,与之前报道的新多毛滴虫微核肌动蛋白I基因中的9个MDSs和8个IESs相比,三列多毛滴虫WR中的微核肌动蛋白I基因由10个MDSs和9个IESs组成。这两个物种中肌动蛋白I基因的MDSs以相似的模式混乱排列,但对于混乱排列的MDSs,MDS-IES连接点的位置最多移动14 bp,对于未混乱排列的MDSs则移动138 bp。MDS-IES连接点的移动导致了重复序列的差异,据信这些重复序列可指导MDS的拼接。此外,这两种多毛滴虫物种微核肌动蛋白I基因中IESs的大小和序列也不同。这些观察结果为IES插入和MDS混乱在进化中的可能起源提供了见解,并显示了寡毛纲中生殖系DNA的非凡可塑性。