Bryan P N, Olah J, Birnstiel M L
Cell. 1983 Jul;33(3):843-8. doi: 10.1016/0092-8674(83)90026-0.
The major histone gene repeat (h22) of the sea urchin Psammechinus miliaris is transiently expressed for several hours during early embryonic development. Several major alterations in chromatin structure coincide with changes in the pattern of early histone gene expression and are reversed later. During the early (128-cell) blastula stages when h22 DNA is maximally expressed, promoter regions of all five histone genes are sensitive to both micrococcal nuclease and DNAase I. Hypersensitivity to micrococcal nuclease remains the same throughout the early hours of development, but disappears abruptly at hatching blastula stage when transcription has completely ceased. Some sequences near the 3' end of active histone genes are very resistant to micrococcal nuclease cutting and map just downstream of the inverted DNA repeats essential for generating faithful 3' ends of histone mRNAs. These same histone DNA sequences are readily cut in free DNA or when histone genes are transcriptionally inactive.
海胆米氏刻肋海胆(Psammechinus miliaris)的主要组蛋白基因重复序列(h22)在胚胎发育早期会短暂表达数小时。染色质结构的几个主要变化与早期组蛋白基因表达模式的变化相吻合,随后会逆转。在早期(128细胞)囊胚阶段,当h22 DNA最大程度表达时,所有五个组蛋白基因的启动子区域对微球菌核酸酶和DNA酶I均敏感。在发育的早期阶段,对微球菌核酸酶的超敏反应保持不变,但在孵化囊胚阶段转录完全停止时突然消失。活性组蛋白基因3'端附近的一些序列对微球菌核酸酶切割具有很强的抗性,并且定位在生成忠实的组蛋白mRNA 3'端所必需的反向DNA重复序列的下游。这些相同的组蛋白DNA序列在游离DNA中或组蛋白基因转录不活跃时很容易被切割。