基于特异性病灶扩增片段测序技术,开发 Aegilops comosa 和 Aegilops caudata 特异性分子标记和荧光原位杂交探针。

IF 6.2 1区 生物学 Q1 PLANT SCIENCES The Plant Journal Pub Date : 2024-11-22 DOI:10.1111/tpj.17140
Yuanyuan Zuo, Shoufen Dai, Xinyu Wang, Jinyue Zhang, Juan Yang, Wen Yang, Haojie Zhao, Na Shu, Pengying Song, Gang Liu, Zehong Yan
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引用次数: 0

摘要

作为小麦的三级基因库,Aegilops comosa 和 Ae. caudata 含有许多优良基因/性状,逐渐成为世界范围内小麦改良的重要野生资源。然而,由于缺乏特异性好、灵敏度高的分子标记和细胞学探针,限制了 Triticum aestivum-Ae. comosa (Ta. Aeco)/Ae. caudata (Ta. Aeca) 引种系的开发和利用。利用特定位点扩增片段测序技术,对两个 Ae. comosa 和一个 Ae. caudata(中国春)以及三个 Ta.Aeco 和 Ta.Aeco 和 Ta. Aeca 引种品系分别进行测序,以开发新的分子标记和细胞学探针。经过严格的序列比对和在不同材料中的验证,共获得 39 个特异于 Comosa Ae. 的三条染色体的分子标记(1M、2M 和 7M 分别有 9 个、7 个和 10 个标记)和 Ae.新开发的分子标记和荧光原位杂交(FISH)探针(一个中心粒探针具有 M 染色体的特异性信号,两个中心粒探针在所有被测基因组中都有信号,6 个、8 个和 4 个 FISH 探针分别具有 M、C 和 M、C、U 染色体的特异性信号)已被成功利用。新开发的分子标记和细胞学探针可用于Aegilops的核型研究和中心粒进化分析,并能检测引种品系中的融合中心粒和小片段易位。
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Development of Aegilops comosa and Aegilops caudata-specific molecular markers and fluorescence in situ hybridization probes based on specific-locus amplified fragment sequencing.

As tertiary gene pools of wheat, Aegilops comosa and Ae. caudata contain many excellent genes/traits and gradually become important and noteworthy wild resources for wheat improvement worldwide. However, the lack of molecular markers and cytological probes with good specificity and high sensitivity limits the development and utilization of Triticum aestivum-Ae. comosa (Ta. Aeco)/Ae. caudata (Ta. Aeca) introgression lines. Using specific-locus amplified fragment sequencing, two Ae. comosa and one Ae. caudata accessions, Chinese Spring, and three Ta. Aeco and Ta. Aeca introgression lines each were sequenced to develop new molecular markers and cytological probes. After strict sequence comparison and verification in different materials, a total of 39 molecular markers specific to three chromosomes in Ae. comosa (nine, seven, and 10 markers for 1M, 2M, and 7M, respectively) and Ae. caudata (two, six, and five markers for 3C, 4C, and 5C, respectively) and 21 fluorescence in situ hybridization (FISH) probes (one centromeric probe with signals specific to the M chromosomes, two centromeric probes with signals in all the tested genomes, and six, eight, and four FISH probes specific to the M, C, and M, C, and U chromosomes, respectively) were successfully exploited. The newly developed molecular markers and cytological probes could be used in karyotype studies, centromere evolutionary analyses of Aegilops, and had the ability to detect the fusion centromeres and small-fragment translocations in introgression lines.

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来源期刊
The Plant Journal
The Plant Journal 生物-植物科学
CiteScore
13.10
自引率
4.20%
发文量
415
审稿时长
2.3 months
期刊介绍: Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community. Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.
期刊最新文献
Development of Aegilops comosa and Aegilops caudata-specific molecular markers and fluorescence in situ hybridization probes based on specific-locus amplified fragment sequencing. Laser dissection-assisted phloem transcriptomics highlights the metabolic and physiological changes accompanying clubroot disease progression in oilseed rape. Disruption of aldehyde dehydrogenase decreases cell wall-bound p-hydroxycinnamates and improves cell wall digestibility in rice. Oxidation of four monoterpenoid indole alkaloid classes by three cytochrome P450 monooxygenases from Tabernaemontana litoralis. RMI1 is essential for maintaining rice genome stability at high temperature.
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