Seigneurin D, Grunwald D, Lawrence J J, Khochbin S
Laboratoire de Biologie Moléculaire du Cycle Cellulaire - INSERM U309, Institut Albert Bonniot, Faculté de Médecine, La Tronche, France.
Int J Dev Biol. 1995 Aug;39(4):597-603.
There exists a close relationship between core histone acetylation and the induced expression of the histone H1(0) gene. We took advantage of this fact to evaluate the influence of chromatin hyperacetylation on the developmentally regulated expression of this specific gene. In this study, the in situ immunodetection approach has been used to analyze both the acetylated histone H4 isoforms and histone H1(0) accumulation during early Xenopus laevis development. We have chosen two stages of development, gastrula stage, when H1(0) is not expressed and not inducible by butyrate treatment, and stage 27 when H1(0) is not expressed but is inducible by butyrate. At stage 27 of development, the early induced accumulation of histone H1(0) under butyrate treatment, occurs mainly in tissues that express the protein normally during later development. These experiments suggest that histone acetylation may be part of a pathway which, in a specific set of cells, keeps H1(0) and probably a series of specific genes, competent for transcription, but cell-specific factors are involved in the induced expression of these genes.
核心组蛋白乙酰化与组蛋白H1(0)基因的诱导表达之间存在密切关系。我们利用这一事实来评估染色质超乙酰化对该特定基因发育调控表达的影响。在本研究中,原位免疫检测方法已被用于分析非洲爪蟾早期发育过程中乙酰化组蛋白H4亚型和组蛋白H1(0)的积累情况。我们选择了两个发育阶段,原肠胚阶段,此时H1(0)不表达且丁酸盐处理不能诱导其表达;以及第27阶段,此时H1(0)不表达但可被丁酸盐诱导。在发育的第27阶段,丁酸盐处理下组蛋白H1(0)的早期诱导积累主要发生在后期发育过程中正常表达该蛋白的组织中。这些实验表明,组蛋白乙酰化可能是一条途径的一部分,在特定的一组细胞中,该途径使H1(0)以及可能一系列特定基因具备转录能力,但细胞特异性因子参与这些基因的诱导表达。