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通过基于寡核苷酸的染色体涂染鉴定出的异源多倍体中的所有非同源染色体及重排。

All nonhomologous chromosomes and rearrangements in × allopolyploids identified by oligo-based painting.

作者信息

Chai Jin, Xue Li, Lei Jiawei, Yao Wei, Zhang Muqing, Deng Zuhu, Yu Fan

机构信息

State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Guangxi University, Nanning, China.

Guangxi Key Laboratory for Sugarcane Biology, Guangxi University, Nanning, China.

出版信息

Front Plant Sci. 2023 Oct 6;14:1176914. doi: 10.3389/fpls.2023.1176914. eCollection 2023.

Abstract

Modern sugarcane cultivars ( spp., 2 = 100~120) are complex polyploids primarily derived from interspecific hybridization between and . Nobilization is the theory of utilizing wild germplasm in sugarcane breeding, and is the foundation for utilizing for stress resistance. However, the exact chromosomal transmission remains elusive due to a lack of chromosome-specific markers. Here, we applied chromosome-specific oligonucleotide (oligo)-based probes for identifying chromosomes 1-10 of the F hybrids between and . Then, -specific repetitive DNA probes were used to distinguish in these hybrids. This oligo- fluorescence hybridization (FISH) system proved to be an efficient tool for revealing individual chromosomal inheritance during nobilization. We discovered the complete doubling of derived chromosomes in most F hybrids. Notably, we also found defective -derived chromosome doubling in the F hybrid Yacheng75-4191, which exhibited 1.5n transmission for all nonhomologous chromosomes. Altogether, these results highlight the presence of variable chromosome transmission in nobilization between and , including 1.5n + n and 2n + n. These findings provide robust chromosome markers for in-depth studies into the molecular mechanism underlying chromosome doubling during the nobilization, as well as tracing chromosomal inheritance for sugarcane breeding.

摘要

现代甘蔗品种( spp.,2n = 100~120)是复杂的多倍体,主要源自 和 之间的种间杂交。高贵化是甘蔗育种中利用野生种质的理论,也是利用 进行抗逆性研究的基础。然而,由于缺乏染色体特异性标记,确切的染色体传递情况仍然不清楚。在此,我们应用基于染色体特异性寡核苷酸(oligo)的探针来鉴定 和 之间F1杂种的1 - 10号染色体。然后,使用 特异性重复DNA探针来区分这些杂种中的 。这种寡核苷酸荧光原位杂交(FISH)系统被证明是揭示高贵化过程中个体染色体遗传的有效工具。我们发现大多数F1杂种中衍生染色体完全加倍。值得注意的是,我们还在F1杂种崖城75 - 4191中发现了有缺陷的 衍生染色体加倍,该杂种对所有非同源染色体均表现出1.5n传递。总之,这些结果突出了 和 之间高贵化过程中存在可变的染色体传递,包括1.5n + n和2n + n。这些发现为深入研究高贵化过程中染色体加倍的分子机制以及甘蔗育种中的染色体遗传追踪提供了强大的染色体标记。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db24/10588481/ca18db83d5d2/fpls-14-1176914-g001.jpg

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