4.5 Article

Transcriptomes and DNA methylomes in apomictic cells delineate nucellar embryogenesis initiation in citrus

期刊

DNA RESEARCH
卷 28, 期 5, 页码 -

出版社

OXFORD UNIV PRESS
DOI: 10.1093/dnares/dsab014

关键词

citrus; apomixis; laser microdissection; RNA-Seq; BS-Seq

资金

  1. Ministry of Science and Technology of China [2018YFD1000106]
  2. National Natural Science Foundation of China [31872051, 31630065]
  3. Fundamental Research Funds for Central Universities [2662018PY013]
  4. Hubei Hongshan Laboratory

向作者/读者索取更多资源

Citrus nucellar poly-embryony is achieved through activation of ribosome biogenesis, protein degradation, and embryogenic development processes, while repressing auxin polar transport and increasing DNA methylation levels to regulate cell fate and NEI cell identity.
Citrus nucellar poly-embryony (NPE) is a mode of sporophytic apomixis that asexual embryos formed in the seed through adventitious embryogenesis from the somatic nucellar cells. NPE allows clonal propagation of rootstocks, but it impedes citrus cross breeding. To understand the cellular processes involved in NPE initiation, we profiled the transcriptomes and DNA methylomes in laser microdissection captured citrus apomictic cells. In apomictic cells, ribosome biogenesis and protein degradation were activated, whereas auxin polar transport was repressed. Reactive oxygen species (ROS) accumulated in the poly-embryonic ovules, and response to oxidative stress was provoked. The global DNA methylation level, especially that of CHH context, was decreased, whereas the methylation level of the NPE-controlling key gene CitRWP was increased. A C2H2 domain-containing transcription factor gene and CitRWP co-expressed specifically in apomictic cells may coordinate to initiate NPE. The activated embryogenic development and callose deposition processes indicated embryogenic fate of nucellar embryo initial (NEI) cells. In our working model for citrus NPE initiation, DNA hyper-methylation may activate transcription of CitRWP, which increases C2H2 expression and ROS accumulation, triggers epigenetic regulation and regulates cell fate transition and NEI cell identity in the apomictic cells.

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