Huang Shengnan, Liu Zhiyong, Li Chengyu, Yao Runpeng, Li Danyang, Hou Li, Li Xiang, Liu Wenjie, Feng Hui
Department of Horticulture, Shenyang Agricultural UniversityShenyang, China.
Front Plant Sci. 2017 Apr 10;8:546. doi: 10.3389/fpls.2017.00546. eCollection 2017.
Female-sterile mutants are ideal materials for studying pistil development in plants. Here, we identified a female-sterile mutant in Chinese cabbage. This mutant, which exhibited stable inheritance, was derived from Chinese cabbage DH line 'FT' using a combination of isolated microspore culture and ethyl methanesulfonate mutagenesis. Compared with the wild-type line 'FT,' the plants exhibited pistil abortion, and floral organs were also relatively smaller. Genetic analysis indicated that the phenotype of is controlled by a single recessive nuclear gene. Morphological observations revealed that the presence of abnormal ovules in likely influenced normal fertilization process, ultimately leading to female sterility. Comparative transcriptome analysis on the flower buds of 'FT' and using RNA-Seq revealed a total of 1,872 differentially expressed genes (DEGs). Of these, a number of genes involved in pistil development were identified, such as (), (), (), and (). Furthermore, GO and KEGG pathway enrichment analyses of the DEGs suggested that a variety of biological processes and metabolic pathways are significantly enriched during pistil development. In addition, the expression patterns of 16 DEGs, including four pistil development-related genes and 12 floral organ development-related genes, were analyzed using qRT-PCR. A total of 31,272 single nucleotide polymorphisms were specifically detected in . These results contribute to shed light on the regulatory mechanisms underlying pistil development in Chinese cabbage.
雌性不育突变体是研究植物雌蕊发育的理想材料。在此,我们鉴定了一个大白菜雌性不育突变体。该突变体表现出稳定的遗传特性,它是通过游离小孢子培养和甲磺酸乙酯诱变相结合的方法,从大白菜双单倍体系‘FT’中获得的。与野生型品系‘FT’相比,该突变体植株表现出雌蕊败育,并且花器官也相对较小。遗传分析表明,该突变体的表型受单个隐性核基因控制。形态学观察发现,该突变体中异常胚珠的存在可能影响了正常的受精过程,最终导致雌性不育。利用RNA-Seq对‘FT’和该突变体的花芽进行比较转录组分析,共鉴定出1872个差异表达基因(DEG)。其中,鉴定出了一些参与雌蕊发育的基因,如(具体基因名称未给出)、(具体基因名称未给出)、(具体基因名称未给出)和(具体基因名称未给出)。此外,对差异表达基因的GO和KEGG通路富集分析表明,在雌蕊发育过程中多种生物学过程和代谢通路显著富集。另外,利用qRT-PCR分析了16个差异表达基因的表达模式,包括4个与雌蕊发育相关的基因和12个与花器官发育相关的基因。在该突变体中特异性检测到了总共31272个单核苷酸多态性。这些结果有助于阐明大白菜雌蕊发育的调控机制。