Dynamics of Known Long Non-Coding RNAs during the Maternal-to-Zygotic Transition in Rabbit

SIMPLE SUMMARY: We first revealed the expression profile of rabbit known lncRNAs during embryo pre-implantation development and showed minor and major wave of zygotic lncRNAs synthesis. The study then selected the differentially expressed (DE) lncRNAs between consecutive stages and predicted their potential target genes. The GO and KEGG analyses suggested that the lncRNAs participate in the regulation of embryo cleavage and development. Additionally, the sequential degradation of maternal lncRNAs showed that, like maternal mRNAs, maternal lncRNAs degradation occurred via maternal and zygotic pathways and the late-degraded lncRNAs might play a role in the degradation of mRNAs through mRNA surveillance pathway. ABSTRACT: The control of pre-implantation development in mammals undergoes a maternal-to-zygotic transition (MZT) after fertilization. The transition involves maternal clearance and zygotic genome activation remodeling the terminal differentiated gamete to confer totipotency. In the study, we first determined the profile of long non-coding RNAs (lncRNAs) of mature rabbit oocyte, 2-cell, 4-cell, 8-cell, and morula embryos using RNA-seq. A total of 2673 known rabbit lncRNAs were identified. The lncRNAs exhibited dynamic expression patterns during pre-implantation development. Moreover, 107 differentially expressed lncRNAs (DE lncRNAs) were detected between mature oocyte and 2-cell embryo, while 419 DE lncRNAs were detected between 8-cell embryo and morula, consistent with the occurrence of minor and major zygotic genome activation (ZGA) wave of rabbit pre-implanted embryo. This study then predicted the potential target genes of DE lncRNAs based on the trans-regulation mechanism of lncRNAs. The GO and KEGG analyses showed that lncRNAs with stage-specific expression patterns promoted embryo cleavage and synchronic development by regulating gene transcription and translation, intracellular metabolism and organelle organization, and intercellular signaling transduction. The correlation analysis between mRNAs and lncRNAs identified that lncRNAs ENSOCUG00000034943 and ENSOCUG00000036338 may play a vital role in the late-period pre-implantation development by regulating ILF2 gene. This study also found that the sequential degradation of maternal lncRNAs occurred through maternal and zygotic pathways. Furthermore, the function analysis of the late-degraded lncRNAs suggested that these lncRNAs may play a role in the mRNA degradation in embryos via mRNA surveillance pathway. Therefore, this work provides a global view of known lncRNAs in rabbit pre-implantation development and highlights the role of lncRNAs in embryogenesis regulation.