Commonwealth Scientific and Industrial Research Organization Plant Industry, Waite Campus, Adelaide, South Australia 5064, Australia.
Plant Physiol. 2013 Sep;163(1):216-31. doi: 10.1104/pp.113.219485. Epub 2013 Jul 17.
Hieracium praealtum forms seeds asexually by apomixis. During ovule development, sexual reproduction initiates with megaspore mother cell entry into meiosis and formation of a tetrad of haploid megaspores. The sexual pathway ceases when a diploid aposporous initial (AI) cell differentiates, enlarges, and undergoes mitosis, forming an aposporous embryo sac that displaces sexual structures. Embryo and endosperm development in aposporous embryo sacs is fertilization independent. Transcriptional data relating to apomixis initiation in Hieracium spp. ovules is scarce and the functional identity of the AI cell relative to other ovule cell types is unclear. Enlarging AI cells with undivided nuclei, early aposporous embryo sacs containing two to four nuclei, and random groups of sporophytic ovule cells not undergoing these events were collected by laser capture microdissection. Isolated amplified messenger RNA samples were sequenced using the 454 pyrosequencing platform and comparatively analyzed to establish indicative roles of the captured cell types. Transcriptome and protein motif analyses showed that approximately one-half of the assembled contigs identified homologous sequences in Arabidopsis (Arabidopsis thaliana), of which the vast majority were expressed during early Arabidopsis ovule development. The sporophytic ovule cells were enriched in signaling functions. Gene expression indicative of meiosis was notably absent in enlarging AI cells, consistent with subsequent aposporous embryo sac formation without meiosis. The AI cell transcriptome was most similar to the early aposporous embryo sac transcriptome when comparing known functional annotations and both shared expressed genes involved in gametophyte development, suggesting that the enlarging AI cell is already transitioning to an embryo sac program prior to mitotic division.
绵毛旋覆花通过无融合生殖形成种子。在胚珠发育过程中,有性生殖始于大孢子母细胞进入减数分裂和形成四个单倍体大孢子的四分体。当二倍体无孢子原基(AI)细胞分化、增大并经历有丝分裂,形成取代有性结构的无孢子胚囊时,有性途径停止。无融合生殖胚囊中的胚胎和胚乳发育与受精无关。关于绵毛旋覆花胚珠无融合生殖起始的转录数据很少,并且 AI 细胞相对于其他胚珠细胞类型的功能身份尚不清楚。通过激光捕获显微切割收集了具有未分裂核的增大 AI 细胞、含有 2 到 4 个核的早期无孢子胚囊以及未经历这些事件的随机孢子体胚珠细胞群。使用 454 焦磷酸测序平台对分离的扩增信使 RNA 样品进行测序,并进行比较分析,以确定捕获细胞类型的指示作用。转录组和蛋白质基序分析表明,大约一半组装的 contigs 鉴定出拟南芥(Arabidopsis thaliana)中的同源序列,其中绝大多数在早期拟南芥胚珠发育过程中表达。孢子体胚珠细胞富含信号功能。在增大的 AI 细胞中,明显缺乏减数分裂的指示基因表达,这与随后无减数分裂的无孢子胚囊形成一致。当比较已知的功能注释时,AI 细胞的转录组与早期无孢子胚囊的转录组最相似,并且两者都共享参与配子体发育的表达基因,这表明在有丝分裂分裂之前,增大的 AI 细胞已经开始向胚囊程序过渡。