首页> 美国卫生研究院文献>Nucleic Acids Research >In vitro deletion analysis of ARS elements spanning the replication origin in the 5 non-transcribed spacer of Tetrahymena thermophila ribosomal DNA.
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In vitro deletion analysis of ARS elements spanning the replication origin in the 5 non-transcribed spacer of Tetrahymena thermophila ribosomal DNA.

机译:ARS元素的体外缺失分析跨越了嗜热四膜膜核糖体DNA 5非转录间隔区的复制起点。

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摘要

Two adjacent but non-overlapping restriction fragments that encompass the replication origin of the macronuclear copy of rDNA from Tetrahymena thermophila allow autonomous replication of plasmids in the yeast Saccharomyces cerevisiae; i.e. they function as autonomously replicating segments (ARS). Deletions generated in vitro into these fragments yield an 82 bp segment from each as the smallest sequence specifying ARS function. These 82 bp segments are at the 5' end of a 220 bp region of homology between the two original ARS restriction fragments. A 39 bp region of almost complete sequence identity between the two 82 bp fragments is suggested to be a core sequence element necessary for ARS function. This 39 bp sequence contains a region identical or nearly identical to the 11 bp yeast ARS consensus sequence (T/ATTTATPuTTTA/T) which is suggested to be essential for ARS function. Detailed comparisons of the 82 bp segments and of the 39 bp core with other ARS sequences reveal no extensive homologies aside from the consensus.
机译:两个相邻但不重叠的限制性片段包括来自嗜热四膜膜虫的rDNA的大核拷贝的复制起点,允许质粒在酿酒酵母中自主复制。即它们充当自主复制段(ARS)。体外产生的这些片段的缺失从每个片段产生一个82 bp的片段,作为指定ARS功能的最小序列。这两个82 bp的片段位于两个原始ARS限制片段之间的220 bp同源性区域的5'末端。两个82 bp片段之间几乎完全相同的39 bp区域被认为是ARS功能必需的核心序列元件。该39bp的序列包含与11bp的酵母ARS共有序列(T / ATTTATPuTTTA / T)相同或几乎相同的区域,提示该序列对于ARS功能是必不可少的。 82 bp片段和39 bp核心与其他ARS序列的详细比较显示,除共有序列外,没有其他同源性。

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