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首页> 外文期刊>The Journal of Reproduction and Development >DNA methylation-mediated transcription factors regulate Piwil1 expression during chicken spermatogenesis
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DNA methylation-mediated transcription factors regulate Piwil1 expression during chicken spermatogenesis

机译:DNA甲基化介导的转录因子在鸡精子形成过程中调节Piwil1表达

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The P-element induced wimpy testis (Piwi) protein family is responsible for initiating spermatogenesis and maintaining the integrity of germ cells and stem cells, but little is known regarding its transcriptional regulation in poultry. Here, we characterized the methylation status of the Piwil1 promoter in five different spermatogenic cell lines using direct bisulfite pyrosequencing and determined that methylation correlates negatively with germ cell type-specific expression patterns of piwil1 . We demonstrated that methylation of the ?148 CpG site, which is the predicted binding site for the transcription factors TCF3 and NRF1, was differentially methylated in different spermatogenic cells. This site was completely methylated in PGCs (primordial germ cells), but was unmethylated in round spermatids. A similar result was obtained in the region from +121 to +139 CpG sites of the Piwil1 promoter CpG island, which was predicted to contain SOX2 binding sites. In addition, demethylation assays further demonstrated that DNA methylation indeed regulates Piwil1 expression during chicken spermatogenesis. Combined with transcription factor binding site prediction, we speculate that methylation influences the recruitment of corresponding transcription factors. Collectively, we show the negative correlation between promoter methylation and piwil1 expression and that the spatiotemporal expression of chicken Piwil1 from the PGC stage to the round spermatid stage is influenced by methylation-mediated transcription factor regulation.
机译:P元素诱导的w弱睾丸(Piwi)蛋白家族负责启动精子发生并维持生殖细胞和干细胞的完整性,但对其在家禽中的转录调控知之甚少。在这里,我们使用直接的亚硫酸氢盐焦磷酸测序技术在五个不同的生精细胞系中表征了Piwil1启动子的甲基化状态,并确定甲基化与piwil1的生殖细胞类型特异性表达模式负相关。我们证明了?148 CpG位点的甲基化,它是转录因子TCF3和NRF1的预测结合位点,在不同的生精细胞中被甲基化。该位点在PGC(原始生殖细胞)中完全甲基化,但在圆形精子细胞中未甲基化。在Piwil1启动子CpG岛的+121至+139 CpG位点区域中获得了相似的结果,该区域预计包含SOX2结合位点。此外,脱甲基化分析进一步证明,DNA甲基化确实在鸡精子发生过程中调节Piwil1表达。结合转录因子结合位点预测,我们推测甲基化影响相应转录因子的募集。总的来说,我们显示了启动子甲基化与piwil1表达之间的负相关性,以及从PGC阶段到圆形精子阶段的鸡Piwil1的时空表达受甲基化介导的转录因子调控的影响。

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