嘌呤负载、茎环和Chargaff第二宇称规则:基本原理在早期化学观察中的应用讨论。

Donald R Forsdyke, Sheldon J Bell
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引用次数: 56

摘要

早在测序技术允许直接计数碱基之前,DNA碱基组成就已经用化学方法测定了。利用现代测序技术所作的一些最近的观察结果,可以通过将基本原理应用于早期的化学观察而推断出来。本文提请注意这样一个事实,即具有重要茎环结构的潜力是单链DNA(基因和非基因)的一般特性,因此对于任何相应的转录本来说,无论它们是凭借其结构(例如rRNA)还是作为mRNA发挥功能。此外,还有Chargaff的第二宇称规则:在单链中,嘌呤的百分比大约等于嘧啶的百分比。由于在茎中,嘌呤与嘧啶匹配,因此Szybalski规则(转录本违反第二宇称规则而有利于嘌呤)必须适用于环。由于嘌呤负载发生在中温和嗜热两种物种中,具有转录本的基因需要稳定的二级结构才能在高温下发挥作用,因此必须通过选择性地增加茎的GC百分比(GC%)来实现这一点,同时保持环的嘌呤负载。认为嘌呤装载对转录本通过二级结构(即rnas,而非mrna)发挥作用的基因的rna同义链环具有特异性的观点,需要考虑作为对照的mrna同义链环区。不考虑基因取向的整个基因或整个基因组不是适当的控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Purine loading, stem-loops and Chargaff's second parity rule: a discussion of the application of elementary principles to early chemical observations.

DNA base compositions were determined chemically long before sequencing technologies permitted the direct counting of bases. Some recent observations made using modern sequencing technologies could have been deduced by application of elementary principles to early chemical observations. This paper draws attention to the fact that the potential for significant stem-loop structure is a general property of single-stranded DNA (genic and non-genic) and hence for any corresponding transcripts, whether they function by virtue of their structure (eg rRNA) or as mRNA. Furthermore, there is Chargaff's second parity rule: in single strands, the percentage of purines approximately equals the percentage of pyrimidines. Since, in stems, purines match pyrimidines, Szybalski's rule that transcripts violate the second parity rule in favour of purines, must apply to loops. Since purine loading occurs in both mesophilic and thermophilic species, genes with transcripts that need stable secondary structures for functioning at high temperatures must achieve this by selectively increasing the GC percentage (GC%) of stems, while retaining purine loading of loops. Arguments that purine loading is specific for the loops of RNA-synonymous strands of genes whose transcripts function by virtue of their secondary structure (ie rRNAs, not mRNAs) need to take into account, as controls, the loop regions of mRNA-synonymous strands. Entire genes, or entire genomes where gene orientation is not considered, are not appropriate controls.

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