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Deciphering Cell Lineage Specification during Male Sex Determination with Single-Cell RNA Sequencing

机译:单细胞RNA测序确定男性性别时破译细胞谱系规范

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Summary The gonad is a unique biological system for studying cell-fate decisions. However, major questions remain regarding the identity of somatic progenitor cells and the transcriptional events driving cell differentiation. Using time-series single-cell RNA sequencing on XY mouse gonads during sex determination, we identified a single population of somatic progenitor cells prior to sex determination. A subset of these progenitors differentiates into Sertoli cells, a process characterized by a highly dynamic genetic program consisting of sequential waves of gene expression. Another subset of multipotent cells maintains their progenitor state but undergoes significant transcriptional changes restricting their competence toward a?steroidogenic fate required for the differentiation of fetal Leydig cells. Our findings confirm the presence of a unique multipotent progenitor population in the gonadal primordium that gives rise to both supporting and interstitial lineages. These also provide the most granular analysis of the transcriptional events occurring during testicular cell-fate commitment.
机译:小结性腺是研究细胞命运决定的独特生物系统。然而,关于体细胞祖细胞的身份和驱动细胞分化的转录事件仍然存在主要问题。在性别确定期间使用XY小鼠性腺上的时间序列单细胞RNA测序,我们在性别确定之前确定了单个的体细胞祖细胞群。这些祖细胞的一个子集分化为支持细胞,该过程的特征是由基因表达的连续波组成的高度动态的遗传程序。多能细胞的另一个子集保持其祖细胞状态,但经历显着的转录变化,从而限制了它们对分化为胎儿Leydig细胞所需的类固醇生成命运的能力。我们的研究结果证实,性腺原基中存在独特的多能祖细胞,从而引起支持性和间质性谱系。这些还提供了对睾丸细胞命运承诺期间发生的转录事件的最详尽的分析。

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