Umek R M, Kowalski D
Nucleic Acids Res. 1987 Jun 11;15(11):4467-80. doi: 10.1093/nar/15.11.4467.
Mung bean nuclease was used to probe for DNA unwinding in torsionally-stressed chimeric plasmids containing two micron plasmid sequences and the yeast LEU2 gene in a pBR322 vector. The yeast sequences are cleaved at only two sites, both of which map to regulatory regions: (1) the autonomously replicating sequence (ARS), an origin of DNA replication, of the two micron plasmid and (2) the transcription terminator region of the LEU2 gene. Nucleotide level analysis of the nuclease cleavage pattern shows that an A + T-rich structure, distinct from other non-B DNA conformations, is recognized. A computer analysis reveals that A + T content alone is not sufficient to explain the preferential occurrence of the A + T-rich structure in the ARS over other sequences of equal A + T content. The A + T-rich structure detected in the ARS maps to sequences required for DNA replication. Our findings demonstrate the DNA conformational flexibility of certain yeast regulatory regions and provide support for the hypothesis that the A + T-rich sequence in the ARS plays a role in DNA unwinding during the initiation of DNA replication.
绿豆核酸酶用于探测含有两个微米质粒序列和位于pBR322载体中的酵母LEU2基因的受扭应力嵌合质粒中的DNA解旋情况。酵母序列仅在两个位点被切割,这两个位点都位于调控区域:(1)两个微米质粒的自主复制序列(ARS),即DNA复制起点;(2)LEU2基因的转录终止区域。对核酸酶切割模式的核苷酸水平分析表明,识别出了一种不同于其他非B型DNA构象的富含A + T的结构。计算机分析显示,仅A + T含量不足以解释ARS中富含A + T的结构比其他具有相同A + T含量的序列更优先出现的情况。在ARS中检测到的富含A + T的结构映射到DNA复制所需的序列。我们的研究结果证明了某些酵母调控区域的DNA构象灵活性,并为ARS中富含A + T的序列在DNA复制起始时的DNA解旋中起作用这一假说提供了支持。