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通过开发一套完整的染色体特异性寡核苷酸探针全面表征……的细胞学特征 。 (注:原文中“by the Development of a Complete Set of Chromosome-Specific Oligo Probes”之前似乎缺失了具体要表征的对象)

Comprehensively Characterizing the Cytological Features of by the Development of a Complete Set of Chromosome-Specific Oligo Probes.

作者信息

Meng Zhuang, Zhang Zhiliang, Yan Tianying, Lin Qingfang, Wang Yu, Huang Weiyuan, Huang Yongji, Li Zhanjie, Yu Qingyi, Wang Jianping, Wang Kai

机构信息

Key Laboratory of Genetics, Breeding and Multiple Utilization of Crops, Ministry of Education, Fujian Provincial Key Laboratory of Haixia Applied Plant Systems Biology, Center for Genomics and Biotechnology, Fujian Agriculture and Forestry University, Fuzhou, China.

Texas A&M AgriLife Research, The Texas A&M University System, Dallas, TX, United States.

出版信息

Front Plant Sci. 2018 Nov 6;9:1624. doi: 10.3389/fpls.2018.01624. eCollection 2018.

Abstract

Chromosome-specific identification is a powerful technique in the study of genome structure and evolution. However, there is no reliable cytogenetic marker to unambiguously identify each of the chromosomes in sugarcane ( spp., Poaceae), which has a complex genome with a high level of ploidy and heterozygosity. In this study, we developed a set of oligonucleotide (oligo)-based probes through bioinformatic design and massive synthetization. These probes produced a clear and bright single signal in each of the chromosomes and their eight homologous chromosomes in the ancient species (2 = 8 = 64). Thus, they can be used as reliable markers to robustly label each of the chromosomes in . We then obtained the karyotype data and established a nomenclature based on chromosomal sizes for the eight chromosomes of the octoploid . In addition, we also found that the 45S and 5S rDNAs demonstrated high copy number variations among different homologous chromosomes, indicating a rapid evolution of the highly repeated sequence after polyploidization. Our fluorescence hybridization (FISH) assay also demonstrated that these probes could be used as cross-species markers between or within the genera of and . By comparing FISH analyses, we discovered that several chromosome rearrangement events occurred in , which might have contributed to the basic chromosome number reduction from 10 in sorghum to 8 in sugarcane. Consistent identification of individual chromosomes makes molecular cytogenetic study possible in sugarcane and will facilitate fine chromosomal structure and karyotype evolution of the genus .

摘要

染色体特异性识别是研究基因组结构和进化的一项强大技术。然而,在甘蔗(禾本科,甘蔗属)中,没有可靠的细胞遗传学标记来明确识别每条染色体,甘蔗具有复杂的基因组,多倍体水平和杂合度都很高。在本研究中,我们通过生物信息学设计和大规模合成开发了一套基于寡核苷酸(oligo)的探针。这些探针在古老物种(2n = 8x = 64)的每条染色体及其八条同源染色体上产生了清晰明亮的单一信号。因此,它们可作为可靠的标记来稳健地标记甘蔗中的每条染色体。然后,我们获得了核型数据,并基于八倍体甘蔗八条染色体的大小建立了命名法。此外,我们还发现45S和5S rDNA在不同同源染色体之间表现出高拷贝数变异,表明多倍化后高度重复序列的快速进化。我们的荧光原位杂交(FISH)分析还表明,这些探针可作为甘蔗属内或属间的跨物种标记。通过比较FISH分析,我们发现甘蔗中发生了几次染色体重排事件,这可能导致了基本染色体数从高粱的10条减少到甘蔗的8条。对单个染色体的一致识别使甘蔗的分子细胞遗传学研究成为可能,并将促进该属精细染色体结构和核型进化的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ec6/6232525/2b28e726485f/fpls-09-01624-g001.jpg

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