4.7 Article

Developmental series of gene expression clarifies maternal mRNA provisioning and maternal-to-zygotic transition in a reef-building coral

Journal

BMC GENOMICS
Volume 22, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12864-021-08114-y

Keywords

Time course; WGCNA; Epigenetics; Resilience; Oocyte; Embryo

Funding

  1. BSF [2016321]
  2. USDA National Institute of Food and Agriculture, Hatch Formula project [1017848]
  3. Dir for Tech, Innovation, & Partnerships
  4. Translational Impacts [2016321] Funding Source: National Science Foundation

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In the Pacific rice coral, four expression peaks were identified, representing maternal complement, two waves of the MZT, and adult expression. Maternal transcripts are dominated by functions related to cell division, methylation, biosynthesis, metabolism, and protein/RNA processing and transport. The two waves of the MZT involve functions related to biosynthesis, cell division, transcription, ion/peptide transport, and cell signaling. Adult expression is enriched for functions related to signaling, metabolism, and ion/peptide transport.
Background: Maternal mRNA provisioning of oocytes regulates early embryogenesis. Maternal transcripts are degraded as zygotic genome activation (ZGA) intensifies, a phenomenon known as the maternal-to-zygotic transition (MZT). Here, we examine gene expression over nine developmental stages in the Pacific rice coral, Montipora capitata, from eggs and embryos at 1, 4, 9, 14, 22, and 36 h-post-fertilization (hpf), as well as swimming larvae (9d), and adult colonies. Results: Weighted Gene Coexpression Network Analysis revealed four expression peaks, identifying the maternal complement, two waves of the MZT, and adult expression. Gene ontology enrichment revealed maternal mRNAs are dominated by cell division, methylation, biosynthesis, metabolism, and protein/RNA processing and transport functions. The first MZT wave occurs from similar to 4-14 hpf and is enriched in terms related to biosynthesis, methylation, cell division, and transcription. In contrast, functional enrichment in the second MZT wave, or ZGA, from 22 hpf-9dpf, includes ion/peptide transport and cell signaling. Finally, adult expression is enriched for functions related to signaling, metabolism, and ion/peptide transport. Our proposed MZT timing is further supported by expression of enzymes involved in zygotic transcriptional repression (Kaiso) and activation (Sox2), which peak at 14 hpf and 22 hpf, respectively. Further, DNA methylation writing (DNMT3a) and removing (TET1) enzymes peak and remain stable past similar to 4 hpf, suggesting that methylome programming occurs before 4 hpf. Conclusions: Our high-resolution insight into the coral maternal mRNA and MZT provides essential baseline information to understand parental carryover effects and the sensitivity of developmental success under increasing environmental stress.

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