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通过非特异性相互作用进行同源染色体识别。

Homologous chromosome recognition via nonspecific interactions.

作者信息

Marshall Wallace F, Fung Jennifer C

出版信息

bioRxiv. 2023 Jun 28:2023.06.09.544427. doi: 10.1101/2023.06.09.544427.

Abstract

In many organisms, most notably Drosophila, homologous chromosomes in somatic cells associate with each other, a phenomenon known as somatic homolog pairing. Unlike in meiosis, where homology is read out at the level of DNA sequence complementarity, somatic homolog pairing takes place without double strand breaks or strand invasion, thus requiring some other mechanism for homologs to recognize each other. Several studies have suggested a "specific button" model, in which a series of distinct regions in the genome, known as buttons, can associate with each other, presumably mediated by different proteins that bind to these different regions. Here we consider an alternative model, which we term the "button barcode" model, in which there is only one type of recognition site or adhesion button, present in many copies in the genome, each of which can associate with any of the others with equal affinity. An important component of this model is that the buttons are non-uniformly distributed, such that alignment of a chromosome with its correct homolog, compared with a non-homolog, is energetically favored; since to achieve nonhomologous alignment, chromosomes would be required to mechanically deform in order to bring their buttons into mutual register. We investigated several types of barcodes and examined their effect on pairing fidelity. We found that high fidelity homolog recognition can be achieved by arranging chromosome pairing buttons according to an actual industrial barcode used for warehouse sorting. By simulating randomly generated non-uniform button distributions, many highly effective button barcodes can be easily found, some of which achieve virtually perfect pairing fidelity. This model is consistent with existing literature on the effect of translocations of different sizes on homolog pairing. We conclude that a button barcode model can attain highly specific homolog recognition, comparable to that seen in actual cells undergoing somatic homolog pairing, without the need for specific interactions. This model may have implications for how meiotic pairing is achieved.

摘要

在许多生物体中,最显著的是果蝇,体细胞中的同源染色体会相互关联,这种现象被称为体细胞同源配对。与减数分裂不同,减数分裂中同源性是在DNA序列互补水平上识别的,体细胞同源配对在没有双链断裂或链侵入的情况下发生,因此需要一些其他机制来使同源染色体相互识别。几项研究提出了一种“特定纽扣”模型,其中基因组中的一系列不同区域,即纽扣,可以相互关联,推测是由结合这些不同区域的不同蛋白质介导的。在这里,我们考虑另一种模型,我们称之为“纽扣条形码”模型,其中只有一种类型的识别位点或粘附纽扣,在基因组中有许多拷贝,每个拷贝都可以以相同的亲和力与其他任何一个相互关联。该模型的一个重要组成部分是纽扣分布不均匀,这样与非同源染色体相比,一条染色体与其正确的同源染色体对齐在能量上更有利;因为要实现非同源对齐,染色体需要机械变形才能使它们的纽扣相互对齐。我们研究了几种类型的条形码,并研究了它们对配对保真度的影响。我们发现,通过根据用于仓库分拣的实际工业条形码来排列染色体配对纽扣,可以实现高保真同源识别。通过模拟随机生成的不均匀纽扣分布,可以很容易地找到许多高效的纽扣条形码,其中一些几乎实现了完美的配对保真度。该模型与关于不同大小易位对同源配对影响的现有文献一致。我们得出结论,纽扣条形码模型可以实现高度特异性的同源识别,与在经历体细胞同源配对的实际细胞中看到的情况相当,而无需特定的相互作用。该模型可能对减数分裂配对如何实现有启示意义。

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Modeling homologous chromosome recognition via nonspecific interactions.通过非特异性相互作用进行同源染色体识别的建模。
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