LIN28A, an RNA-binding protein, plays an important role in porcine induced pluripotent stem cells (piPSCs). However, the molecular mechanism underlying the function of in the maintenance of pluripotency in piPSCs remains unclear. Here, we explored the function of in piPSCs based on its overexpression and knockdown. We performed total RNA sequencing (RNA-seq) of piPSCs and detected the expression levels of relevant genes by quantitative real-time polymerase chain reaction (qRT-PCR), western blot analysis, and immunofluorescence staining. Results indicated that piPSC proliferation ability decreased following knockdown. Furthermore, when expression in the LIN28A2 group was lower (by 20%) than that in the negative control knockdown group ( NC), the pluripotency of piPSCs disappeared and they differentiated into neuroectoderm cells. Results also showed that overexpression inhibited the expression of (dual-specificity phosphatases) family phosphatases and activated the mitogen-activated protein kinase (MAPK) signaling pathway. Thus, appears to activate the MAPK signaling pathway to maintain the pluripotency and proliferation ability of piPSCs. Our study provides a new resource for exploring the functions of in piPSCs.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8175949 | PMC |
http://dx.doi.org/10.24272/j.issn.2095-8137.2020.375 | DOI Listing |
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