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首页> 外文期刊>Chromosome Research >Asymmetric distribution of histones during Drosophila male germline stem cell asymmetric divisions
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Asymmetric distribution of histones during Drosophila male germline stem cell asymmetric divisions

机译:果蝇雄性生殖细胞干细胞不对称分裂过程中组蛋白的不对称分布。

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It has long been known that epigenetic changes are inheritable. However, except for DNA methylation, little is known about the molecular mechanisms of epigenetic inheritance. Many types of stem cells undergo asymmetric cell divisions to generate self-renewed stem cells and daughter cells committed for differentiation. Still, whether and how stem cells retain their epigenetic memory remain questions to be elucidated. During the asymmetric division of Drosophila male germline stem cell (GSC), our recent studies revealed that the preexisting histone 3 (H3) are selectively segregated to the GSC, whereas newly synthesized H3 deposited during DNA replication are enriched in the differentiating daughter cell. We propose a two-step model to explain this asymmetric histone distribution. First, prior to mitosis, preexisting histones and newly synthesized histones are differentially distributed at two sets of sister chromatids. Next, during mitosis, the set of sister chromatids that mainly consist of preexisting histones are segregated to GSCs, while the other set of sister chromatids enriched with newly synthesized histones are partitioned to the daughter cell committed for differentiation. In this review, we apply current knowledge about epigenetic inheritance and asymmetric cell division to inform our discussion of potential molecular mechanisms and the cellular basis underlying this asymmetric histone distribution pattern. We will also discuss whether this phenomenon contributes to the maintenance of stem cell identity and resetting chromatin structure in the other daughter cell for differentiation.
机译:早就知道表观遗传的变化是可遗传的。但是,除了DNA甲基化外,对表观遗传的分子机制知之甚少。许多类型的干细胞会经历不对称细胞分裂,以产生自我更新的干细胞和致力于分化的子细胞。尽管如此,干细胞是否以及如何保留其表观遗传记忆仍然是有待阐明的问题。在果蝇雄性生殖系干细胞(GSC)的不对称分裂过程中,我们最近的研究表明,先前存在的组蛋白3(H3)被选择性地分离到GSC,而在DNA复制过程中沉积的新合成的H3在分化的子细胞中富集。我们提出了一个两步模型来解释这种不对称的组蛋白分布。首先,在有丝分裂之前,先前存在的组蛋白和新合成的组蛋白差异分布在两组姐妹染色单体上。接下来,在有丝分裂期间,主要由预先存在的组蛋白组成的姐妹染色单体组被分离到GSC,而另一组富含新合成组蛋白的姐妹染色单体被分配到致力于分化的子细胞。在这篇综述中,我们应用了有关表观遗传和不对称细胞分裂的最新知识,以指导我们对潜在分子机制和这种不对称组蛋白分布模式背后的细胞基础的讨论。我们还将讨论这种现象是否有助于维持干细胞的身份并重置另一个子细胞中的染色质结构以进行分化。

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