Chadwick B P, Willard H F
Department of Genetics, Case Western Reserve University School of Medicine and Center for Human Genetics and Research Institute, University Hospitals of Cleveland, 10900 Euclid Avenue, Cleveland, OH 44106-4955, USA.
Hum Mol Genet. 2001 May 1;10(10):1101-13. doi: 10.1093/hmg/10.10.1101.
MacroH2A1 is an unusual variant of the core histone H2A which is enriched in chromatin on the inactive X chromosome of female mammals. The N-terminal third of the protein shares 65% amino acid identity with core histone H2A, while the remaining two-thirds of the protein are novel, with a small stretch of basic amino acids and a putative leucine zipper motif. We have now cloned a second macroH2A gene, encoding macroH2A2 which shares 80% amino acid identity with macroH2A1. Despite mapping to different chromosomes, the genomic organization of the macroH2A2 and macroH2A1 genes are nearly identical. The leucine zipper motif of macroH2A1 is not conserved in macroH2A2. Like macroH2A1, macroH2A2 forms a Macro Chromatin Body in the nuclei of female cells which is coincident with an X chromosome and co-localizes with macroH2A1. To address the distribution of other histone H2A variants in relation to macroH2A and the inactive X chromosome, we constructed a series of epitope-tagged versions of other histone H2A variants. Like the recently described H2A-Bbd (Barr body-deficient) variant, the histone variant H2A.Z was found to be deficient in chromatin on the inactive X chromosome in a significant proportion of female nuclei. This study provides further information about the nucleosomal composition of chromatin on the inactive X chromosome and indicates that a number of H2A variants are non-randomly distributed on the active and inactive X chromosomes.
MacroH2A1是核心组蛋白H2A的一种特殊变体,在雌性哺乳动物失活的X染色体的染色质中含量丰富。该蛋白质的N端三分之一与核心组蛋白H2A具有65%的氨基酸同一性,而其余三分之二的蛋白质是新的,有一小段碱性氨基酸和一个假定的亮氨酸拉链基序。我们现已克隆了第二个macroH2A基因,其编码的macroH2A2与macroH2A1具有80%的氨基酸同一性。尽管定位于不同的染色体,但macroH2A2和macroH2A1基因的基因组组织几乎相同。macroH2A1的亮氨酸拉链基序在macroH2A2中不保守。与macroH2A1一样,macroH2A2在雌性细胞的细胞核中形成一个Macro染色质体,该染色质体与一条X染色体重合,并与macroH2A1共定位。为了研究其他组蛋白H2A变体相对于macroH2A和失活X染色体的分布情况,我们构建了一系列其他组蛋白H2A变体的表位标记版本。与最近描述的H2A-Bbd(巴氏小体缺陷)变体一样,在相当比例的雌性细胞核中,组蛋白变体H2A.Z在失活X染色体的染色质中缺乏。这项研究提供了关于失活X染色体上染色质核小体组成的进一步信息,并表明一些H2A变体在活性和失活X染色体上呈非随机分布。