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Origin and Evolution of B Chromosomes in the Cichlid Fish Astatotilapia latifasciata Based on Integrated Genomic Analyses

机译:基于综合基因组分析的慈鲷鱼Astatotilapia latifasciataB染色体的起源与进化

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摘要

Approximately 15 of eukaryotes contain supernumerary B chromosomes. When present, B chromosomes frequently represent as much as 5 of the genome. Despite thousands of reports describing the distribution of supernumeraries in various taxa, a comprehensive theory for the origin, maintenance, and evolution of B chromosomes has not emerged. Here, we sequence the complete genomes of individual cichlid fish (Astatotilapia latifasciata) with and without B chromosomes, as well as microdissected B chromosomes, to identify DNA sequences on the B. B sequences were further analyzed through quantitative polymerase chain reaction and in situ hybridization. We find that the B chromosome contains thousands of sequences duplicated from essentially every chromosome in the ancestral karyotype. Although most genes on the B chromosome are fragmented, a few are largely intact, and we detect evidence that at least three of them are transcriptionally active. We propose a model in which the B chromosome originated early in the evolutionary history of Lake Victoria cichlids from a small fragment of one autosome. DNA sequences originating from several autosomes, including protein-coding genes and transposable elements, subsequently inserted into this proto-B. We propose that intact B chromosome genes involved with microtubule organization, kinetochore structure, recombination and progression through the cell cycle may play a role in driving the transmission of the B chromosome. Furthermore, our work suggests that karyotyping is an essential step prior to genome sequencing to avoid problems in genome assembly and analytical biases created by the presence of high copy number sequences on the B chromosome.
机译:大约 15% 的真核生物含有多余的 B 染色体。当存在时,B 染色体通常占基因组的 5%。尽管有数以千计的报告描述了各种分类群中编外人员的分布,但尚未出现关于B染色体起源、维持和进化的综合理论。在这里,我们对有和没有B染色体的单个慈鲷鱼(Astatotilapia latifasciata)以及显微解剖的B染色体的完整基因组进行测序,以鉴定B上的DNA序列。我们发现 B 染色体包含数千个序列,这些序列基本上与祖先核型中的每条染色体都重复。尽管B染色体上的大多数基因都是片段化的,但少数基因基本完整,我们发现其中至少有三个基因具有转录活性。我们提出了一个模型,其中B染色体起源于维多利亚湖慈鲷进化历史的早期,来自一个常染色体的一小部分。来自几个常染色体的DNA序列,包括蛋白质编码基因和转座元件,随后插入到这个原B中。我们认为,参与微管组织、动粒结构、重组和细胞周期进程的完整 B 染色体基因可能在驱动 B 染色体的传递中发挥作用。此外,我们的研究表明,核型分析是基因组测序之前必不可少的一步,以避免基因组组装问题和因 B 染色体上存在高拷贝数序列而产生的分析偏差。

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