菜豆(Phaseolus vulgaris)抗炭疽病基因的渗入

Gonzaz Kyaruzi Kazimoto, S. Nchimbi–Msolla, R. Mabagala
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摘要

摘要Kazimoto GK, Nchimbi-Msolla SF, Mabagala RB。2022. 菜豆(Phaseolus vulgaris)抗炭疽病基因的渗入。细胞生物学进展6:20-31。由真菌炭疽菌(Colletotrichum lindemuthium)引起的普通豆炭疽病造成了严重的产量损失。它在低温和高湿度(90-100%)的地区最具破坏性。该研究旨在利用常规育种方法将抗性基因引入适应但敏感的马赛红(Masai Red)和恩贾诺(Soya Njano)当地品种。从坦桑尼亚北部采集的32份常见豆病植物样品中分离出5个小种并命名。抗性基因来源为大豆品种G2333和AB136。在坦桑尼亚北部高地曼雅拉地区的Bashnet,在高海拔和潮湿环境的野外条件下对早期发达种群进行了评估。Njano x G2333的F2和F3群体均以9:7的比例分离出对黄枯草病菌的抗性。这种分离表明两个显性上位基因从G2333遗传而来,抗性是以上位基因相互作用的方式产生的。Masai Red x G2333与F2和F3群体的杂交分离比为10:6,表明两个显性抗性基因转移到了发达群体。黄豆与AB136杂交获得的F2和F3后代比例为3:1。马赛红与AB136杂交F2后代的分离比为3:1,F3后代的分离比为3:1。3:1的比例证实单显性基因遗传给发育后代。Njano × G2333和Masai Red × G2333群体的遗传力(h²)在0.41 ~ 0.45之间。而Njano、Masai Red和A136的遗传力在0.2 ~ 0.53之间,遗传力中等。开发的F2和F3种群需要使用MAS进一步检测,以确认抗性基因的存在。应进行多地点试验,以验证已发育的豆类种群在后代中的抗性水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Introgression of anthracnose resistance gene(s) into common bean (Phaseolus vulgaris)
Abstract. Kazimoto GK, Nchimbi-Msolla SF, Mabagala RB. 2022. Introgression of anthracnose resistance gene(s) into common bean (Phaseolus vulgaris). Cell Biol Dev 6: 20-31. Common bean anthracnose disease caused by the fungus Colletotrichum lindemuthianum causes significant yield losses. It is most destructive in areas with cool temperatures and high humidity (90-100%). The study aimed to introduce resistance genes into adapted but susceptible local cultivars of Masai Red and Soya Njano using conventional breeding methods. Five races of C. lindemuthianum were isolated and named from thirty-two common bean-diseased plant samples collected from Northern Tanzania. The sources of resistant genes were bean cultivars G2333 and AB136. Early developed populations were evaluated under field conditions in high altitude and humid environments at Bashnet in the Manyara region, in the Northern highlands of Tanzania. Both F2 and F3 populations of Soya Njano x G2333 were segregated for C. lindemuthianum resistance at a 9:7 ratio. Such segregation implied that two dominant epistatic genes conferred from G2333, the resistance being in the mode of epistatic gene interaction. The crosses between Masai Red x G2333 and F2 and F3 populations segregation ratio was 10:6, implying two dominant resistant genes were transferred to developed populations. The F2 and F3 progenies obtained from crossing Soya Njano and AB136 showed a ratio of 3:1. The F2 progenies from a cross between Masai Red and AB136 were segregated at a ratio of 3:1 and F3 progenies were 3:1. The 3:1 ratio confirmed single dominant gene inheritance conferred to developed progenies. The heritability (h²) from populations of Soya Njano x G2333 and Masai Red x G2333 was between 0.41 and 0.45. While Soya Njano, Masai Red, and A136 were between 0.2 and 0.53, which implied moderate heritability. F2 and F3 populations developed need further testing using MAS to confirm the presence of resistant genes. Multi-location testing should be done to verify the resistance levels of the developed bean population in later generations.
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