Kim Kyeongmin, Kang Yuna, Lee Sol-Ji, Choi Se-Hyun, Jeon Dong-Hyun, Park Min-Young, Park Suhyoung, Lim Yong Pyo, Kim Changsoo
Department of Crop Science, College of Agricultural and Life Sciences, Chungnam National University, Daejeon 34134, Korea.
National Institute of Horticultural & Herbal Science, Rural Development Administration (RDA), Wanju 55365, Korea.
Genes (Basel). 2020 Mar 21;11(3):337. doi: 10.3390/genes11030337.
The radish is a highly self-incompatible plant, and consequently it is difficult to produce homozygous lines. Bud pollination in cross-fertilization plants should be done by opening immature pollen and attaching pollen to mature flowers. It accordingly takes a lot of time and effort to develop lines with fixed alleles. In the current study, a haploid breeding method has been applied to obtain homozygous plants in a short period of time by doubling chromosomes through the induction of a plant body in the haploid cells, in order to shorten the time to breed inbred lines. We constructed genetic maps with an F1 population derived by crossing parents that show a superior and inferior ability to regenerate microspores, respectively. Genetic maps were constructed from the maternal and parental maps, separately, using the two-way pseudo-testcross model. The phenotype of the regeneration rate was examined by microspore cultures and a quantitative trait loci (QTL) analysis was performed based on the regeneration rate. From the results of the culture of microspores in the F1 population, more than half of the group did not regenerate, and only a few showed a high regeneration rate. A total of five significant QTLs were detected in the F1 population, and five candidate genes were found based on the results. These candidate genes are divided into two classes, and appear to be related to either PRC2 subunits or auxin synthesis.
萝卜是一种高度自交不亲和的植物,因此很难培育出纯合品系。对于异花授粉植物,芽授粉应通过打开未成熟花粉并将花粉附着到成熟花朵上来进行。因此,培育具有固定等位基因的品系需要花费大量的时间和精力。在本研究中,应用了单倍体育种方法,通过在单倍体细胞中诱导植物体加倍染色体,在短时间内获得纯合植株,以缩短培育自交系的时间。我们利用分别具有优、劣小孢子再生能力的亲本杂交得到的F1群体构建了遗传图谱。使用双向伪测交模型分别从母本图谱和父本图谱构建遗传图谱。通过小孢子培养检测再生率的表型,并基于再生率进行数量性状位点(QTL)分析。从F1群体小孢子培养的结果来看,超过一半的群体没有再生,只有少数表现出高再生率。在F1群体中总共检测到5个显著的QTL,并根据结果发现了5个候选基因。这些候选基因分为两类,似乎与PRC2亚基或生长素合成有关。