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Uncoupling of transcriptomic and cytological differentiation in mouse spermatocytes with impaired meiosis

机译:减数分裂受损的小鼠精母细胞转录组学和细胞学分化的解偶联

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摘要

Cell differentiation is driven by changes in gene expression that manifest as changes in cellular phenotype or function. Altered cellular phenotypes, stemming from genetic mutations or other perturbations, are widely assumed to directly correspond to changes in the transcriptome and vice versa. Here, we exploited the cytologically well-defined Prdm9 mutant mouse as a model of developmental arrest to test whether parallel programs of cellular differentiation and gene expression are tightly coordinated, or can be disassociated. By comparing cytological phenotype markers and transcriptomes in wild-type and mutant spermatocytes, we identified multiple instances of cellular and molecular uncoupling in Prdm9–/– mutants. Most notably, although Prdm9–/– germ cells undergo cytological arrest in a late-leptotene/zygotene stage, they nevertheless develop gene expression signatures characteristic of later developmental substages. These findings suggest that transcriptomic changes may not reliably map to cellular phenotypes in developmentally perturbed systems.
机译:细胞分化由基因表达的变化驱动,这些变化表现为细胞表型或功能的变化。广泛认为,由于基因突变或其他干扰而引起的细胞表型改变,直接对应于转录组的变化,反之亦然。在这里,我们利用细胞学上定义明确的Prdm9突变小鼠作为发育停滞的模型,以测试细胞分化和基因表达的平行程序是否紧密协调或可以解除关联。通过比较野生型和突变型精母细胞的细胞学表型标记和转录组,我们鉴定了Prdm9 – / – 突变体中细胞和分子解偶联的多种情况。最值得注意的是,尽管Prdm9 – / – 生殖细胞在晚期瘦素/合子期经历了细胞学停滞,但它们仍发育出后期发育子阶段所特有的基因表达特征。这些发现表明,转录组的变化可能无法可靠地映射到发育受到干扰的系统中的细胞表型。

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