Analysis of chromatin accessibility in p53 deficient spermatogonial stem cells for high frequency transformation into pluripotent state.

Abstract

ObjectivesSpermatogonial stem cells (SSCs), the germline stem cells (GSCs) committed to spermatogenesis in niche, can transform into pluripotent state in long‐term culture without introduction of exogenous factors, typically in p53 deficiency condition. As the guardian for genomic stability, p53 is associated with epigenetic alterations during SSCs transformation. However, the mechanism is still unknown, since complicated roles of p53 baffle our understanding of the regulating process.Materials and MethodsThe chromatin accessibility and differentially expressed genes (DEGs) were analysed in p53 +/+ and p53 −/− SSCs using the Assay for Transposase‐Accessible Chromatin with high‐throughput Sequencing (ATAC‐seq) and RNA‐sequencing (RNA‐seq), to explore the connection of p53 and cell fate at chromosomal level.ResultsSeveral transcription factors (TFs), such as CTCF, SMAD3 and SOX2, were predicted as important factors mediating the transformation. Molecular evidence suggested that SMAD3 efficiently promoted pluripotency‐associated gene expression both in fresh and long‐term cultured SSCs. However, p53 knockout (KO) is insufficient to induce SMAD3 expression in SSCs.ConclusionsThese observations indicate that SMAD3 is a key factor for SSCs transformation, and an unknown event is required to activate SMAD3 as the prerequisite for SSCs reprogramming, which may occur in the long‐term culture of SSCs. This study demonstrates the connection of p53 and pluripotency‐associated factors, providing new insight for understanding the mechanisms of SSCs reprogramming and germline tumorigenesis.