Atsuchi Y, Tashiro K, Yamana K, Shiokawa K
Department of Biology, Faculty of Science 33, Kyushu University, Fukuoka, Japan.
J Embryol Exp Morphol. 1986 Nov;98:175-85.
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.
利用克隆的组蛋白H4 cDNA作为探针,通过Northern印迹分析,追踪非洲爪蟾早期发育过程中每个胚胎的组蛋白H4 mRNA含量。在囊胚期之前,H4 mRNA含量几乎保持恒定,在原肠胚期大幅增加,然后在神经胚期下降。放线菌素D实验表明,在原肠胚后期和神经胚期检测到的大多数H4 mRNA分子的维持依赖于这些阶段H4基因的新转录。为了观察H4 mRNA水平是否受细胞黏附的影响,我们制备了解离细胞,并在抑制细胞重新聚集的条件下测量H4 mRNA含量。结果发现,解离且抑制重新聚集的细胞中每个胚胎的H4 mRNA量几乎与神经胚期对照胚胎的相等。因此,我们得出结论,组蛋白H4 mRNA的合成活性在发育过程中不依赖于细胞黏附。