Ma Jun, Zhao Fangyuan, Zhang Yinxia, Tian Xinhui, Du Wenhua
Key Laboratory of Grassland Ecosystem of Ministry of Education, Pratacultural Engineering Laboratory of Gansu Province, Sino-U.S. Centers for Grazingland Ecosystem Sustainability, Collage of Pratacultural Science, Gansu Agricultural University, Lanzhou, Gansu, 730070, China.
Plant Methods. 2025 Jan 7;21(1):2. doi: 10.1186/s13007-024-01322-z.
The rapid production of doubled haploids by anther culture technology is an important breeding method for awnless triticale. The aim of this study was to explore the effects of triticale genotype and the types and ratios of exogenous hormones in the medium on the efficiency of triticale anther culture.
Anthers of five triticale genotypes were cultured on four different callus induction media and the calli were induced to differentiate into green plants by culture on three different differentiation media. The triticale genotype T8004 showed the best performance in anther culture, with a callus induction rate of 28.64%, a green plantlet differentiation frequency of 33.33%, and a green plantlet production rate of 2.78%. The highest callus induction rates were obtained by culturing anthers on C3 medium (the main components were potassium nitrate, glutamine, inositol, etc.), and the highest green plantlet differentiation frequency was obtained by culturing calli on D2 differentiation medium (the main components were potassium nitrate, ammonium nitrate, calcium chloride dihydrate, etc.). Flow cytometry analyses showed that 15 of the 20 DH0 generation plants that grew normally in the field were doubled haploids. The average chromosome doubling success rate was 55.6%. Analyses of agronomic traits showed that the 11 DH1 doubled haploid plants reached the standard for awnless triticale, so they are candidate materials for breeding new awnless triticale varieties.
The anther culture technology of triticale was optimized in this paper, which made it possible to rapidly breed homozygous varieties of awnless triticale.
通过花药培养技术快速获得双单倍体是无芒小黑麦的一种重要育种方法。本研究旨在探讨小黑麦基因型以及培养基中外源激素的种类和比例对小黑麦花药培养效率的影响。
将5个小黑麦基因型的花药接种在4种不同的愈伤组织诱导培养基上培养,然后将愈伤组织接种在3种不同的分化培养基上诱导分化成绿苗。小黑麦基因型T8004在花药培养中表现最佳,愈伤组织诱导率为28.64%,绿苗分化频率为33.33%,绿苗获得率为2.78%。在C3培养基(主要成分有硝酸钾、谷氨酰胺、肌醇等)上培养花药可获得最高的愈伤组织诱导率,在D2分化培养基(主要成分有硝酸钾、硝酸铵、二水氯化钙等)上培养愈伤组织可获得最高的绿苗分化频率。流式细胞仪分析表明,在田间正常生长的20株DH0代植株中有15株为双单倍体,平均染色体加倍成功率为55.6%。农艺性状分析表明,11株DH1代双单倍体植株达到了无芒小黑麦的标准,可作为无芒小黑麦新品种选育的候选材料。
本文优化了小黑麦花药培养技术,为快速培育无芒小黑麦纯合品种提供了可能。