Cloning yeast telomeres on linear plasmid vectors

生物 四膜虫 质粒 端粒 酵母 自主复制序列 遗传学 克隆载体 酿酒酵母 限制地图 复制的起源 DNA 重组DNA 基因 载体(分子生物学)
作者
Jack W. Szostak,Elizabeth H. Blackburn
出处
期刊:Cell [Cell Press]
卷期号:29 (1): 245-255 被引量:625
标识
DOI:10.1016/0092-8674(82)90109-x
摘要

We have constructed a linear yeast plasmid by joining fragments from the termini of Tetrahymena ribosomal DNA to a yeast vector. Structural features of the terminus region of the Tetrahymena rDNA plasmid maintained in the yeast linear plasmid include a set of specifically placed single-strand interruptions within the cluster of hexanucleotide (C4A2) repeat units. An artificially constructed hairpin terminus was unable to stabilize a linear plasmid in yeast. The fact that yeast can recognize and use DNA ends from the distantly related organism Tetrahymena suggests that the structural features required for telomere replication and resolution have been highly conserved in evolution. The linear plasmid was used as a vector to clone chromosomal telomeres from yeast. One Tetrahymena end was removed by restriction digestion, and yeast fragments that could function as an end on a linear plasmid were selected. Restriction mapping and hybridization analysis demonstrated that these fragments were yeast telomeres, and suggested that all yeast chromosomes might have a common telomere sequence. Yeast telomeres appear to be similar in structure to the rDNA of Tetrahymena, in which specific nicks or gaps are present within a simple repeated sequence near the terminus of the DNA.
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