Department of Agricultural, Food and Environmental Sciences, University of Perugia, Perugia, 06121, Italy.
Laboratory of Genomics, Department of Agriculture Food Natural resources Animals and Environment (DAFNAE), University of Padova, 35020, Legnaro, PD, Italy.
Sci Rep. 2018 Feb 14;8(1):3030. doi: 10.1038/s41598-018-21220-4.
Apomixis (asexual reproduction through seeds) is considered a deviation of the sexual reproductive pathway leading to the development of clonal progenies genetically identical to the mother plant. Here we used the Methylation-Sensitive Amplification Polymorphism (MSAP) technique to characterize cytosine methylation patterns occurring in florets of sexual and aposporous Paspalum notatum genotypes, in order to identify epigenetically-controlled genes putatively involved in apomixis development. From twelve polymorphic MSAP-derived sequences, one (PN_6.6, later renamed PN_SCD1) was selected due to its relevant annotation and differential representation in apomictic and sexual floral transcriptome libraries. PN_SCD1 encodes the DENN domain/WD repeat-containing protein SCD1, which interacts with RAB GTPases- and/or MAPKs to promote specialized cell division, functions in clathrin-mediated membrane transport and acts as potential substrate receptor of CUL4 E3 ubiquitin ligases. Quantitative RT-PCR and comparative RNAseq analyses of laser microdissected nucellar cells confirmed PN_SCD1 upregulation in florets of apomictic plants and revealed that overexpression takes place just before the onset of apospory initials. Moreover, we found that several SCD1 molecular partners are expressed in P. notatum florets and upregulated in apomictic plants. Our results disclosed a specific vesicle trafficking molecular pathway epigenetically modulated during apomixis.
无融合生殖(通过种子进行的无性繁殖)被认为是偏离了有性生殖途径,导致克隆后代在遗传上与母株完全相同。在这里,我们使用甲基化敏感扩增多态性(MSAP)技术来描述有性和无融合生殖的 Paspalum notatum 基因型小花中的胞嘧啶甲基化模式,以鉴定可能参与无融合生殖发育的受表观遗传控制的基因。从 12 个多态性 MSAP 衍生序列中,选择了一个(PN_6.6,后来更名为 PN_SCD1),因为它的相关注释和在无融合生殖和有性花转录组文库中的差异表达。PN_SCD1 编码 DENN 结构域/WD 重复蛋白 SCD1,它与 RAB GTPases 和/或 MAPKs 相互作用,以促进特化细胞分裂,在网格蛋白介导的膜运输中起作用,并作为 CUL4 E3 泛素连接酶的潜在底物受体。激光微切割珠心细胞的定量 RT-PCR 和比较 RNAseq 分析证实了 PN_SCD1 在无融合生殖植物小花中的上调,并表明过表达发生在无融合生殖起始之前。此外,我们发现 SCD1 的几个分子伴侣在 P. notatum 小花中表达,并在无融合生殖植物中上调。我们的结果揭示了无融合生殖过程中受表观遗传调控的特定囊泡运输分子途径。