首页> 美国卫生研究院文献>Molecular and Cellular Biology >Suppressible and nonsuppressible +1 G-C base pair insertions induced by ICR-170 at the his4 locus in Saccharomyces cerevisiae.
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Suppressible and nonsuppressible +1 G-C base pair insertions induced by ICR-170 at the his4 locus in Saccharomyces cerevisiae.

机译:由ICR-170在酿酒酵母中his4位点诱导的可抑制和不可抑制的+1 G-C碱基对插入。

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摘要

Fifteen independent ICR-170-induced his4 mutations in Saccharomyces cerevisiae were examined by DNA sequence analysis. All of the mutations contained a +1 G-C base pair addition in the HIS4 coding region. Eleven different sites of insertion were identified. Combined with previous DNA sequence data, 21 ICR-170-induced his4 mutations distributed at 16 different sites were analyzed. The insertions were always located in a consecutive run of two or more G-C base pairs, with all base pairs in each run having identical orientation. Long consecutive G-C runs were preferred target sites over short runs. Although some consecutive G-C runs appeared to be preferred target sites over others of identical length, such preference was not due to any particular type of nucleotide pair immediately adjacent to a given target site. In addition, DNA sequence analyses of the his4 mutations provided a basis for examining the mechanism of mRNA sequence recognition by extragenic suppressors of ICR-170-induced mutations. The implications of these results for mechanisms of frameshift suppression are discussed.
机译:通过DNA序列分析检查了酿酒酵母中的15个独立的ICR-170诱导的his4突变。所有突变均在HIS4编码区中包含+1 G-C碱基对。确定了十一个不同的插入位点。结合先前的DNA序列数据,分析了分布在16个不同位点的21个ICR-170诱导的his4突变。插入片段始终位于两个或多个G-C碱基对的连续序列中,每个序列中的所有碱基对都具有相同的方向。长期连续G-C运行是短期目标的首选目标站点。尽管一些连续的G-C序列似乎是比相同长度的其他序列更优选的靶标位点,但这种优先选择并不是由于与给定靶标位点紧邻的任何特定类型的核苷酸对。此外,对his4突变的DNA序列分析为检查ICR-170诱导的突变的外源抑制剂抑制mRNA序列识别的机制提供了基础。讨论了这些结果对移码抑制机制的影响。

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