Wolffe A P
Laboratory of Molecular Embryology, National Institute of Child Health and Human Development, NIH, Bethesda, MD 20892-5431, USA.
Reprod Nutr Dev. 1996;36(6):581-606.
Major transitions in chromosome and chromatin structure occur during development. Recent genetic and biochemical experiments demonstrate that these alterations in genome organization make significant contributions to establishing and maintaining states of differential transcriptional activity. Developmentally regulated changes in histone variants have a causal role in determining patterns of gene activity, directing the repression of specific eukaryotic genes. Chromosomal proteins such as Polycomb stabilize and maintain transcriptionally repressed states. Proteins regulating mitotic chromosome condensation have a role in determining the overall transcriptional activity of a chromosome. In this review, I place the developmental roles of these chromosomal constituents in a structural and functional context. Considerable insight now exists into the molecular mechanisms regulating chromosomal activity during development. Chromosomal architecture is emerging as a key controlling influence in the developmental regulation of gene expression. Recent genetic experiments using Caenorhabditis elegans, Drosophila melanogaster and the mouse have provided clear evidence for the functional differentiation of chromosomal structures during development. Chromosomes are visualized as highly specialized entities, within which the activity of particular domains is largely determined by defined structural proteins. At a more local level, the mechanisms regulating gene transcription during early embryogenesis in Xenopus and the mouse have been found to be dependent on the biochemical composition of individual nucleosomes. Thus, variation in the type and modification of chromosomal and chromatin structural proteins provides a dominant means of controlling the transcriptional activity of individual genes, individual chromosomal domains and of entire chromosomes. The focus of this review is to summarize these recent advances and to discuss their implications for developmental biology.
染色体和染色质结构的重大转变发生在发育过程中。最近的遗传学和生物化学实验表明,基因组组织的这些改变对建立和维持差异转录活性状态做出了重大贡献。组蛋白变体在发育过程中受到调控的变化在决定基因活性模式、指导特定真核基因的抑制方面具有因果作用。诸如多梳蛋白等染色体蛋白稳定并维持转录抑制状态。调节有丝分裂染色体凝聚的蛋白质在决定染色体的整体转录活性方面发挥作用。在这篇综述中,我将这些染色体成分的发育作用置于结构和功能背景中进行探讨。目前对于发育过程中调控染色体活性的分子机制已经有了相当深入的了解。染色体结构正逐渐成为基因表达发育调控中的关键控制因素。最近利用秀丽隐杆线虫、黑腹果蝇和小鼠进行的遗传学实验为发育过程中染色体结构的功能分化提供了明确证据。染色体被视为高度特化的实体,其中特定结构域的活性很大程度上由特定的结构蛋白决定。在更局部的层面上,已经发现非洲爪蟾和小鼠早期胚胎发育过程中调控基因转录的机制依赖于单个核小体的生化组成。因此,染色体和染色质结构蛋白的类型和修饰变化提供了一种控制单个基因、单个染色体结构域以及整个染色体转录活性的主要方式。本综述的重点是总结这些最新进展,并讨论它们对发育生物学的意义。