首页> 外文期刊>Journal of Cell Science >CHROMATIN MODIFICATIONS DURING OOGENESIS IN THE MOUSE - REMOVAL OF SOMATIC SUBTYPES OF HISTONE H1 FROM OOCYTE CHROMATIN OCCURS POST-NATALLY THROUGH A POST-TRANSCRIPTIONAL MECHANISM
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CHROMATIN MODIFICATIONS DURING OOGENESIS IN THE MOUSE - REMOVAL OF SOMATIC SUBTYPES OF HISTONE H1 FROM OOCYTE CHROMATIN OCCURS POST-NATALLY THROUGH A POST-TRANSCRIPTIONAL MECHANISM

机译:小鼠卵母细胞发生过程中的染色质修饰-通过转录后机制从卵细胞染色质发生中去除组蛋白H1的体细胞亚型H1。

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We examined the distribution of the somatic subtypes of histone H1 and the variant subtype, H1(0), and their encoding mRNAs during oogenesis and early embryogenesis in the mouse, As detected using immunocytochemistry, somatic H1 was present in the nuclei of oocytes of 18-day embryos. Following birth, however, somatic H1 became less abundant in both growing and non-growing oocytes, beginning as early as 4 days of age in the growing oocytes, and was scarcely detectable by 19 days, Together with previous results, this defines a period of time when somatic H1 is depleted in oocytes, namely, from shortly after birth when the oocytes are at prophase I until the 4-cell stage following fertilization, At the stages when somatic H1 was undetectable, oocyte nuclei could be stained using an antibody raised against histone H1(0), which suggests that this may be a major linker histone in these cells, In contrast to the post-natal loss of somatic H1 protein, mRNAs encoding four (H1a, H1b, H1d, H1e) of the five somatic subtypes were present, as detected using RT-PCR in growing oocytes of 9-day pups, and all five subtypes including H1c were present in fully grown oocytes of adults, All five subtypes were also present in embryos, both before and after activation of the embryonic genome, mRNA encoding H1(0) was also detected in oocytes and early embryos, Whole-mount in situ hybridization using cloned H1c and H1e cDNAs revealed that the mRNAs were present in the cytoplasm of oocytes and 1-cell embryos, in contrast to the sea urchin early embryo where they are sequestered in the cell nucleus, We suggest that, as in many somatic cell types, the chromatin of mouse oocytes becomes depleted of somatic H1 and relatively enriched in histone H1(0) postnatally, and that somatic H1 is reassembled onto chromatin in cleavage-stage embryos, The post-natal loss of somatic H1 appears to be regulated post-transcriptionally by a mechanism not involving nuclear localization. [References: 66]
机译:我们检查了组蛋白H1的体细胞亚型和变体亚型H1(0)的分布,以及它们在小鼠卵子发生和早期胚胎发生过程中的编码mRNA,使用免疫细胞化学检测,体细胞H1存在于18个卵母细胞的细胞核中天胚胎。但是,出生后,生长和未生长的卵母细胞中的体细胞H1含量都开始降低,早在生长的卵母细胞中开始为4天,到19天几乎无法检测到。卵母细胞中的体细胞H1耗尽的时间,即从出生后不久,即卵母细胞处于前期I到受精后的4细胞阶段,在无法检测到体细胞H1的阶段,可以使用针对H1的抗体对卵母细胞核进行染色组蛋白H1(0),表明这可能是这些细胞中的主要接头组蛋白,与出生后体细胞H1蛋白的丢失相反,mRNA编码五个体细胞亚型中的四种(H1a,H1b,H1d,H1e)使用RT-PCR在9天幼仔的卵母细胞中检测到存在,包括H1c在内的所有五种亚型均在成年人的成年卵母细胞中存在,在胚胎激活前后,这五种亚型也均存在于胚胎中gen例如,在卵母细胞和早期胚胎中也检测到了编码H1(0)的mRNA。与克隆的H1c和H1e cDNA进行的全装载原位杂交表明,mRNA存在于卵母细胞和1细胞胚胎的细胞质中。海胆早期胚胎,它们被隔离在细胞核中,我们建议,如同在许多体细胞类型中一样,小鼠卵母细胞的染色质在出生后会耗尽体H1,而相对富含组蛋白H1(0),而体H1是重组卵裂期胚胎中的染色质,出生后体细胞H1的丢失似乎是转录后通过不涉及核定位的机制进行调节的。 [参考:66]

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