Wolffe A P, Khochbin S, Dimitrov S
Laboratory of Molecular Embryology, National Institute of Child Health and Human Development, NIH, Bethesda, MD 20892-5430, USA.
Bioessays. 1997 Mar;19(3):249-55. doi: 10.1002/bies.950190311.
Knockout experiments in Tetrahymena show that linker histone H1 is not essential for nuclear assembly or cell viability. These results, together with a series of biochemical and cell biological observations, challenge the existing paradigm that requires linker histones to be a key organizing component of higher-order chromatin structure. The H1 knockouts also reveal a much more subtle role for H1. Instead of acting as a general transcriptional repressor, H1 is found to regulate a limited number of specific genes. Surprisingly, H1 can both activate and repress transcription. We discuss how this architectural protein might accomplish this important regulatory role.
对四膜虫进行的基因敲除实验表明,连接组蛋白H1对于细胞核组装或细胞生存力并非必不可少。这些结果,连同一系列生化和细胞生物学观察结果,对现有的范式提出了挑战,该范式认为连接组蛋白是高阶染色质结构的关键组织成分。H1基因敲除实验还揭示了H1更为微妙的作用。H1并非作为一般的转录抑制因子起作用,而是发现它能调节有限数量的特定基因。令人惊讶的是,H1既能激活转录,也能抑制转录。我们讨论了这种结构蛋白可能如何完成这一重要的调节作用。