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利用寡核苷酸荧光原位杂交(Oligo-FISH)鉴定菊花属物种的 5S 和 45S rDNA 位点。

Identification of 5S and 45S rDNA sites in Chrysanthemum species by using oligonucleotide fluorescence in situ hybridization (Oligo-FISH).

机构信息

State Key Laboratory of Crop Genetics and Germplasm Enhancement, Key Laboratory of Landscaping, Ministry of Agriculture, College of Horticulture, Nanjing Agricultural University, Nanjing, China.

出版信息

Mol Biol Rep. 2021 Jan;48(1):21-31. doi: 10.1007/s11033-020-06102-1. Epub 2021 Jan 17.

Abstract

Fluorescence in situ hybridization (FISH) is a conventional method used to visualize the distribution of DNA elements within a genome. To examine the relationships within the Chrysanthemum genus, ribosomal DNA (rDNA), a popular cytogenetic marker, was utilized as a probe for FISH within this genus. Based on the genome data of Chrysanthemum nankingense, C. seticuspe and its allied genera in the Compositae(Asteraceae), we explored rDNA sequences to design oligonucleotide probes and perform oligonucleotide fluorescence in situ hybridization (Oligo-FISH) in eight Chrysanthemum accessions. The results showed that the majority of 5S rDNA signals were located in subterminal chromosome regions and that the number of 5S rDNA sites might be tightly associated with ploidy. For 45S rDNA sites, the number and intensity of signals differed from those of previously investigated Chrysanthemum resources. These findings may provide an optimally reliable method of examining the chromosome composition and structural variation of Chrysanthemum and its related species and allow researchers to understand the evolutionary history and phylogenetic relationships of Chrysanthemum.

摘要

荧光原位杂交(FISH)是一种常规方法,用于可视化基因组内 DNA 元素的分布。为了研究菊花属内的关系,核糖体 DNA(rDNA)作为一种染色体遗传标记,被用作该属内 FISH 的探针。基于菊花属的南京菊、舌状花野菊及其菊科(菊科)近缘属的基因组数据,我们探索了 rDNA 序列以设计寡核苷酸探针,并在 8 个菊花品种中进行了寡核苷酸荧光原位杂交(Oligo-FISH)。结果表明,大多数 5S rDNA 信号位于末端染色体区域,并且 5S rDNA 位点的数量可能与倍性密切相关。对于 45S rDNA 位点,信号的数量和强度与之前研究的菊花资源不同。这些发现可能为研究菊花及其相关物种的染色体组成和结构变异提供一种优化的可靠方法,并使研究人员能够了解菊花的进化历史和系统发育关系。

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