{"title":"基因组遵守查尔加夫的第二条奇偶性规则可能是非适应性的,但茎环现在的功能是适应性的","authors":"Donald R. Forsdyke","doi":"10.1016/j.jtbi.2024.111943","DOIUrl":null,"url":null,"abstract":"<div><p>Of Chargaff’s four rules on DNA base quantity, his second parity rule (PR-2) is the most contentious. Various biometricians (e.g., Sueoka, Lobry) regarded PR-2 compliance as a non-adaptive feature of modern genomes that could be modeled through interrelations among mutation rates. However, PR-2 compliance with stem-loop potential was considered adaptively relevant by biochemists familiar with analyses of nucleic acid structure (e.g., of Crick) and of meiotic recombination (e.g., of Kleckner). Meanwhile, other biometricians had shown that PR-2 complementarity extended beyond individual bases (1-mers) to oligonucleotides (k-mers), possibly reflecting “advantageous DNA structure” (Nussinov). An “introns early” hypothesis (Reanney, Forsdyke) had suggested a primordial nucleic acid world with recombination-mediated error-correction requiring genome-wide stem-loop potential to have evolved prior to localized intrusions of protein-encoding potential (exons). Thus, a primordial genome was equivalent to one long intron. Indeed, when assessed as the base order-dependent component (correcting for local influences of GC%), modern genes, especially when evolving rapidly under positive Darwinian selection, display high intronic stem-loop potential. This suggests forced migration from neighboring exons by competing protein-encoding potential. PR-2 compliance may have first arisen non-adaptively. Primary prototypic structures were later strengthened by their adaptive contribution to recombination. 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Various biometricians (e.g., Sueoka, Lobry) regarded PR-2 compliance as a non-adaptive feature of modern genomes that could be modeled through interrelations among mutation rates. However, PR-2 compliance with stem-loop potential was considered adaptively relevant by biochemists familiar with analyses of nucleic acid structure (e.g., of Crick) and of meiotic recombination (e.g., of Kleckner). Meanwhile, other biometricians had shown that PR-2 complementarity extended beyond individual bases (1-mers) to oligonucleotides (k-mers), possibly reflecting “advantageous DNA structure” (Nussinov). An “introns early” hypothesis (Reanney, Forsdyke) had suggested a primordial nucleic acid world with recombination-mediated error-correction requiring genome-wide stem-loop potential to have evolved prior to localized intrusions of protein-encoding potential (exons). Thus, a primordial genome was equivalent to one long intron. Indeed, when assessed as the base order-dependent component (correcting for local influences of GC%), modern genes, especially when evolving rapidly under positive Darwinian selection, display high intronic stem-loop potential. This suggests forced migration from neighboring exons by competing protein-encoding potential. PR-2 compliance may have first arisen non-adaptively. Primary prototypic structures were later strengthened by their adaptive contribution to recombination. 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引用次数: 0
摘要
在查尔格夫关于 DNA 碱基数量的四条规则中,他的第二条奇偶性规则(PR-2)最具争议性。各种生物计量学家(如 Sueoka、Lobry)认为,PR-2 符合性是现代基因组的一个非适应性特征,可以通过突变率之间的相互关系来模拟。然而,熟悉核酸结构分析(如克里克的分析)和减数分裂重组分析(如克莱克纳的分析)的生物化学家认为,PR-2 与茎环潜力的顺应性与适应性相关。与此同时,其他生物计量学家已经证明,PR-2互补性超越了单个碱基(1-mers),扩展到寡核苷酸(k-mers),可能反映了 "有利的DNA结构"(努西诺夫)。内含子早期 "假说(Reanney,Forsdyke)认为,原始核酸世界具有重组介导的纠错功能,要求在蛋白质编码潜能(外显子)局部侵入之前,整个基因组的茎环潜能已经进化。因此,原始基因组相当于一个长内含子。事实上,当评估与碱基顺序有关的成分时(校正 GC% 的局部影响),现代基因,尤其是在达尔文正向选择下快速进化的基因,显示出较高的内含子茎环潜力。这表明,相邻外显子的蛋白质编码潜能竞争迫使基因迁移。PR-2顺应性最初可能是非适应性产生的。初级原型结构后来因其对重组的适应性贡献而得到加强。因此,有争议的观点实际上可能是一致的。
Genomic compliance with Chargaff’s second parity rule may have originated non-adaptively, but stem-loops now function adaptively
Of Chargaff’s four rules on DNA base quantity, his second parity rule (PR-2) is the most contentious. Various biometricians (e.g., Sueoka, Lobry) regarded PR-2 compliance as a non-adaptive feature of modern genomes that could be modeled through interrelations among mutation rates. However, PR-2 compliance with stem-loop potential was considered adaptively relevant by biochemists familiar with analyses of nucleic acid structure (e.g., of Crick) and of meiotic recombination (e.g., of Kleckner). Meanwhile, other biometricians had shown that PR-2 complementarity extended beyond individual bases (1-mers) to oligonucleotides (k-mers), possibly reflecting “advantageous DNA structure” (Nussinov). An “introns early” hypothesis (Reanney, Forsdyke) had suggested a primordial nucleic acid world with recombination-mediated error-correction requiring genome-wide stem-loop potential to have evolved prior to localized intrusions of protein-encoding potential (exons). Thus, a primordial genome was equivalent to one long intron. Indeed, when assessed as the base order-dependent component (correcting for local influences of GC%), modern genes, especially when evolving rapidly under positive Darwinian selection, display high intronic stem-loop potential. This suggests forced migration from neighboring exons by competing protein-encoding potential. PR-2 compliance may have first arisen non-adaptively. Primary prototypic structures were later strengthened by their adaptive contribution to recombination. Thus, contentious views may actually be in harmony.
期刊介绍:
The Journal of Theoretical Biology is the leading forum for theoretical perspectives that give insight into biological processes. It covers a very wide range of topics and is of interest to biologists in many areas of research, including:
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