Long non-coding RNA lnc_3712 impedes nuclear reprogramming via repressing Kdm5b

ABSTRACT: Long non-coding RNAs (lncRNAs) are involved in shaping chromosome conformation and regulation of preimplantation development. However, the role of lncRNA during somatic cell nuclear transfer (SCNT) reprogramming remains largely unknown. In the present study, we identified 114 upregulated lncRNAs in the 8-cell SCNT embryos as candidate key molecules involved in nuclear reprogramming in goat. We found that H3K4me3 was an epigenetic barrier in goat nuclear reprogramming that and injection of Kdm5b mRNA greatly improved SCNT embryos development through removal of H3K4me3. We further reported that knockdown of lnc_3712 increased the expression of Kdm5b, which led to H3K4me3 demethylation. Of note, the development of goat SCNT embryos was improved when lnc_3712 was knocked down, whereas the blastocyst rate showed no difference in lnc_3712 and Kdm5b double knockdown SCNT embryos compared with the negative control SCNT embryos. Specifically, in lnc_3712 knockdown SCNT embryos, partial of the transcriptional activity and the expression of critical embryonic genes (Wee1, Ctsb, and Ybx1) were similar with that of in vitro fertilization embryos. Therefore, our results elucidate the critical role of lnc_3712 in regulating the development of goat SCNT embryos via repressing Kdm5b, which advances our current understanding of the role of lncRNAs during nuclear reprogramming. Graphical Abstract Deng and colleagues provide the lncRNA profile in goat SCNT embryos and show that knockdown of lncRNA lnc_3712 increases the expression of Kdm5b and demethylates H3K4me3, resulting in improvement of goat SCNT embryo development, which broadens the current understanding of the role of lncRNAs during the stochastic reprogramming events.

SUBMITTER: Deng M 

PROVIDER: S-EPMC7940708 | biostudies-literature |

REPOSITORIES: biostudies-literature