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三种大鼠基因组的限制性内切酶分析及分子分析,特别涉及染色体重排和物种形成问题。

Restriction endonuclease and molecular analyses of three rat genomes with special reference to chromosome rearrangement and speciation problems.

作者信息

Miklos G L, Willcocks D A, Baverstock P R

出版信息

Chromosoma. 1980;76(3):339-63. doi: 10.1007/BF00327271.

Abstract

When differences are found between related species of organisms, it is often assumed that the differences themselves are causal factors either in speciation itself or in processes related to speciation. Two recent proposals on the functions of satellite DNA (Hatch et al., 1976 and Fry and Salser 1977) are that (a) large amounts of satellite DNA are important in facilitating chromosome rearrangements and hence cytogenetic evolution, and (b) satellite DNA differences between homologous chromosomes lead to pairing difficulties and are important in generating infertility barriers and hence speciation. If these proposals were to have some generality, one could expect organisms with very low amounts of highly repeated DNA to exhibit few chromosome rearrangements and to be evolutionarily conservative in a cytogenetic sense.--We have chosen two very closely related species of rat which are phenotypically almost indistinguishable and which have undergone massive genome reorganization. They differ by 11 major centric rearrangements (2n = 32, 2n = 50). We have characterised their genomes by restriction endonuclease digestions, thermal denaturations, analytical ultracentrifugations and reassociation techniques, and have found that they have virtually no highly repeated DNA. Thus the 11 major chromosomal rearrangements have been fixed in present day genomes with hardly any highly repeated DNA, centric or otherwise.--It appears therefore, that a large amount of highly repeated DNA is not obligatory for the formation and fixation of chromosome rearrangements. In addition, the existing literature reveals that one can find almost any situation at all, from species groups with high amounts of satellite DNA and no gross chromosomal rearrangements, to ones such as those described here, with tiny amounts of highly repeated DNA and massive chromosomal reorganisation. Since direct experimental data indicates that satellite DNA differences per se between homologous chromosomes do not cause infertility, speculations concerning modes of speciation based on satellite DNA differences between otherwise homologous chromosomes would appear to be ill founded.

摘要

当在相关生物物种之间发现差异时,人们常常认为这些差异本身就是物种形成过程或与物种形成相关过程中的因果因素。最近关于卫星DNA功能的两项提议(哈奇等人,1976年;弗莱和萨尔泽,1977年)是:(a)大量卫星DNA在促进染色体重排从而推动细胞遗传学进化方面很重要;(b)同源染色体之间的卫星DNA差异会导致配对困难,在产生不育障碍进而导致物种形成方面很重要。如果这些提议具有一定普遍性,那么人们可能会预期具有极低量高度重复DNA的生物表现出很少的染色体重排,并且在细胞遗传学意义上是进化保守的。——我们选择了两种非常近缘的大鼠物种,它们在表型上几乎无法区分,并且经历了大规模的基因组重组。它们在11次主要的着丝粒重排上存在差异(2n = 32,2n = 50)。我们通过限制性内切酶消化、热变性、分析超速离心和重退火技术对它们的基因组进行了表征,发现它们几乎没有高度重复DNA。因此,这11次主要的染色体重排在当今基因组中得以固定,几乎没有任何高度重复DNA,无论是着丝粒相关的还是其他类型的。——因此,似乎大量高度重复DNA对于染色体重排的形成和固定并非必不可少。此外,现有文献表明,从具有大量卫星DNA且无明显染色体重排的物种组,到像这里所描述的具有极少量高度重复DNA且有大规模染色体重组的物种组,几乎各种情况都能找到。由于直接的实验数据表明同源染色体之间的卫星DNA差异本身不会导致不育,基于同源染色体之间卫星DNA差异的物种形成模式的推测似乎没有根据。

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