Chau M F, Orias E
Department of Molecular, Cellular and Developmental Biology, University of California, Santa Barbara 93106, USA.
Biol Cell. 1996;86(2-3):111-20. doi: 10.1016/0248-4900(96)84773-3.
Extensive developmentally programmed DNA rearrangements, including thousands of internal deletions, occur in the differentiating somatic macronucleus in Tetrahymena thermophila. Some deletion systems involve the use of multiple alternative deletion sites. We report here the cloning and the sequences of three new alternative deletion systems (RR, RP and B) obtained using genomic subtraction. The RP and RR deletion systems are 2 kb apart on chromosome 1R, and both involve the removal of < 2 kb of micronuclear sequences. The B deletion system is on chromosome 5 and involves a deletion of > 5 kb. All three deleted regions are very AT rich (approximately 80%) and do not appear to encode any protein. Sequences of the regions flanking the deletion junctions of all three systems revealed no sequence similarity among them nor with any previously reported deletion systems, suggesting that different cis-acting elements are involved for rearrangement. Unlike other deletion systems in ciliates, the B deletion system lacks short terminal direct repeats. Our results suggest an average of at least one alternative deletion system per 134 kb of micronuclear DNA and lead to an estimate that at least 25% of all deletion systems in Tetrahymena utilize alternative ends. The genomic subtraction method employed in this study could prove useful for the isolation of alternatively deleted DNA in special-purpose cases in Tetrahymena and other ciliates. The hybridization parameters for genomic subtraction worked out here for highly AT-rich DNA may have wider usefulness.
在嗜热四膜虫分化的体大核中发生了广泛的发育编程性DNA重排,包括数千次内部缺失。一些缺失系统涉及使用多个替代缺失位点。我们在此报告通过基因组扣除获得的三个新的替代缺失系统(RR、RP和B)的克隆及序列。RP和RR缺失系统在1R染色体上相距2 kb,二者都涉及去除小于2 kb的小核序列。B缺失系统位于5号染色体上,涉及大于5 kb的缺失。所有三个缺失区域都富含AT(约80%),且似乎不编码任何蛋白质。所有三个系统缺失连接侧翼区域的序列在它们之间以及与任何先前报道的缺失系统之间均未显示出序列相似性,这表明重排涉及不同的顺式作用元件。与纤毛虫中的其他缺失系统不同,B缺失系统缺乏短末端直接重复序列。我们的结果表明,平均每134 kb小核DNA至少有一个替代缺失系统,并由此估计四膜虫中至少25%的缺失系统利用替代末端。本研究中采用的基因组扣除方法可能被证明在分离四膜虫和其他纤毛虫特殊情况下的替代缺失DNA时有用。此处针对高度富含AT的DNA得出的基因组扣除杂交参数可能具有更广泛的用途。