BCAT- based marker for marker-assisted selection in Vietnam cucumber breeding

Phuong Tran Dong Nguyen, Ngan Hieu Luong, Phuong Thi Bich Ho, Kinh Thi Le, Linh Thi Truc Le
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引用次数: 1

Abstract

Yield imporovement is one of the major breeding objectives of cucumber improvement. Gynoecious, an important agricultural trait which highly correlates with yield, was proved to be controlled by F locus. Conventional plant breeding approach has some limitations in term of potential inaccuracies and time-consuming. Molecular marker-assisted breeding is, therefore, an effective alternative solution. F locus– linked molecular marker has been reported previously. The main aim of this project was to evaluate the potential applicability of this F locus–specific marker for marker–assisted selection in Vietnam cucumber breeding program. Three different cucumber populations e.g., pure lines, F2 and F3 population were utilized with 13, 131 and 84 plants, respectively for each population. Plant sexual phenotypes were determined. Sequencing reactions were performed for BCAT 3’UTR of 3 gynoecious and 2 monoecious pure lines. Plant genotypes were determined by standard PCR with a primer pair amplifying a 56 bp-deletion region in BCAT 3’UTR. A 56 bp-deletion was found in BCAT 3’UTR of gynoecious pure lines as compared with monoecious lines. The marker based on this 56 bp-deletion region in BCAT 3’UTR could help to separate cucumber plants having homozygous and heterozygous sex phenotypes. The marker genotype absolutely corresponded with monoecious trait. Especially, the marker could precisely explain for 80 % gynoecious trait. The marker highly explained for Vietnam cucumber sex traits and could be applied for marker-assisted selection in cucumber breeding program in Vietnam in future.
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基于BCAT的标记辅助选择在越南黄瓜育种中的应用
产量提高是黄瓜改良育种的主要目标之一。雌同株是与产量高度相关的重要农业性状,经证实受F位点控制。传统的植物育种方法在潜在的不准确性和耗时方面存在一定的局限性。因此,分子标记辅助育种是一种有效的替代解决方案。F位点连锁分子标记以前有报道。本项目的主要目的是评估该F位点特异性标记在越南黄瓜育种计划中的标记辅助选择的潜在适用性。利用黄瓜纯系、F2和F3 3个不同群体,每个群体分别有13株、131株和84株。测定植物性表型。对3个雌雄同株和2个雌雄同株纯系的BCAT 3′utr进行测序反应。采用标准PCR方法确定植物基因型,引物对扩增BCAT 3'UTR中56 bp缺失区域。与雌雄同株相比,雌交纯系BCAT 3′utr缺失56个bp。基于BCAT 3'UTR中56 bp缺失区域的标记可用于区分纯合子和杂合子性表型的黄瓜植株。标记基因型与雌雄同株性状完全一致。特别是,该标记可以精确地解释80%的雌雄同体性状。该标记对越南黄瓜的性性状具有较高的解释力,可用于今后越南黄瓜育种中的标记辅助选择。
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