Blomberg P, Randolph C, Yao C H, Yao M C
Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98104, USA.
Mol Cell Biol. 1997 Dec;17(12):7237-47. doi: 10.1128/MCB.17.12.7237.
We have analyzed the cis-acting sequences that regulate rRNA gene (rDNA) replication in Tetrahymena thermophila. The macronucleus of this ciliated protozoan contains 9,000 copies of a 21-kbp minichromosome in the form of a palindrome comprising two copies of the rDNA. These are derived from a single chromosomally integrated copy during conjugation through selective amplification and are maintained by replicating once per cell cycle during vegetative growth. We have developed a transformation vector and carried out a deletion analysis to determine the minimal sequences required for replication, amplification, and/or stable maintenance of the rDNA molecule. Using constructs containing progressively longer deletions, we show that only a small portion (approximately 900 bp) of the rDNA is needed for extrachromosomal replication and stable maintenance of this molecule. This core region is very near but does not include the rRNA transcription initiation site or its putative promoter, indicating that replication is not dependent on normal rRNA transcription. It includes two nearly identical nuclease-sensitive domains (D1 and D2), one of which (D1) corresponds to the physical origin of replication determined previously. Deletion of both domains abolishes replication, whereas deletion of either domain allows the molecules to replicate, indicating that only one domain is required. In addition to this core region, we have found several DNA segments, including a tandem array of a 21-nucleotide repeat (type II repeats) and sequences within the rRNA coding region, that play distinctive and important roles in maintaining the rDNA at a high copy number.
我们分析了调控嗜热四膜虫核糖体RNA基因(rDNA)复制的顺式作用序列。这种纤毛原生动物的大核含有9000个21千碱基对的微型染色体拷贝,呈回文结构,包含两份rDNA。这些拷贝在接合过程中通过选择性扩增从单个染色体整合拷贝衍生而来,并在营养生长期间每个细胞周期复制一次得以维持。我们构建了一个转化载体并进行了缺失分析,以确定rDNA分子复制、扩增和/或稳定维持所需的最小序列。使用包含逐渐延长缺失片段的构建体,我们发现,对于该分子的染色体外复制和稳定维持,仅需要rDNA的一小部分(约900碱基对)。这个核心区域非常靠近但不包括rRNA转录起始位点或其假定的启动子,这表明复制不依赖于正常的rRNA转录。它包括两个几乎相同的核酸酶敏感结构域(D1和D2),其中一个(D1)与先前确定的物理复制起点相对应。两个结构域都缺失会消除复制,而缺失任何一个结构域都允许分子进行复制,这表明仅需要一个结构域。除了这个核心区域,我们还发现了几个DNA片段,包括一个21核苷酸重复序列的串联阵列(II型重复序列)和rRNA编码区域内的序列,它们在将rDNA维持在高拷贝数方面发挥着独特而重要的作用。