Level of histone H4 mRNA in Xenopus laevis embryonic cells cultured in the absence of cell adhesion.

Y Atsuchi, K Tashiro, K Yamana, K Shiokawa
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Abstract

The amount of histone H4 mRNA per embryo was followed during early development of Xenopus laevis by Northern blot analyses using a cloned histone H4 cDNA as the probe. The H4 mRNA content was nearly constant until the blastula stage, increased greatly at the gastrula stage and then decreased at the neurula stage. Experiments with actinomycin D suggested that most H4 mRNA molecules detected at the late gastrula and neurula stages were maintained depending on new transcription of H4 genes during these stages. To see if the H4 mRNA level is affected by cell adhesion, we prepared dissociated cells and measured H4 mRNA content under conditions that inhibit cellular reaggregation. It was found that the amount of H4 mRNA per embryo in dissociated and reaggregation-inhibited cells was nearly equal to that of the control embryo at the neurula stage. Therefore, we conclude that the synthetic activity of histone H4 mRNA is not dependent on the cellular adhesion during development.

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无黏附条件下非洲爪蟾胚胎细胞组蛋白H4 mRNA水平的变化。
以克隆的组蛋白H4 cDNA为探针,采用Northern blot方法对非洲爪蟾发育早期每个胚胎中组蛋白H4 mRNA的表达量进行分析。H4 mRNA含量在胚期前基本保持不变,在原肠期显著升高,在神经期显著降低。放线菌素D的实验表明,在原肠期晚期和神经期检测到的大多数H4 mRNA分子在这些阶段依靠H4基因的新转录得以维持。为了观察H4 mRNA的水平是否受到细胞粘附的影响,我们制备了游离细胞,并在抑制细胞再聚集的条件下测量了H4 mRNA的含量。结果发现,在神经胚期,分离和再聚集抑制细胞中每个胚胎的H4 mRNA含量与对照胚胎几乎相等。因此,我们得出结论,组蛋白H4 mRNA的合成活性不依赖于发育过程中的细胞粘附。
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