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首页> 外文期刊>Developmental cell >Resolution of cell fate decisions revealed by single-cell gene expression analysis from zygote to blastocyst.
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Resolution of cell fate decisions revealed by single-cell gene expression analysis from zygote to blastocyst.

机译:从合子到胚泡的单细胞基因表达分析揭示了细胞命运决定的解决方案。

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摘要

Three distinct cell types are present within the 64-cell stage mouse blastocyst. We have investigated cellular development up to this stage using single-cell expression analysis of more than 500 cells. The 48 genes analyzed were selected in part based on a whole-embryo analysis of more than 800 transcription factors. We show that in the morula, blastomeres coexpress transcription factors specific to different lineages, but by the 64-cell stage three cell types can be clearly distinguished according to their quantitative expression profiles. We identify Id2 and Sox2 as the earliest markers of outer and inner cells, respectively. This is followed by an inverse correlation in expression for the receptor-ligand pair Fgfr2/Fgf4 in the early inner cell mass. Position and signaling events appear to precede the maturation of the transcriptional program. These results illustrate the power of single-cell expression analysis to provide insight into developmental mechanisms. The technique should be widely applicable to other biological systems.
机译:在64细胞阶段的小鼠胚泡中存在三种不同的细胞类型。我们已经使用超过500个细胞的单细胞表达分析研究了到这一阶段的细胞发育。根据对800多个转录因子的全胚分析,部分选择了48个被分析的基因。我们显示在桑ula中,卵裂球共表达特定于不同谱系的转录因子,但是通过64细胞阶段,根据其定量表达谱可以清楚地区分三种细胞类型。我们将Id2和Sox2分别识别为外部细胞和内部细胞的最早标记。其次是早期内细胞团中受体-配体对Fgfr2 / Fgf4的表达呈负相关。位置和信号事件似乎在转录程序成熟之前。这些结果说明了单细胞表达分析的力量,可提供对发育机制的深入了解。该技术应广泛适用于其他生物系统。

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