Kagotani Kazuhiro, Takebayashi Shin-ichiro, Kohda Atsushi, Taguchi Hiroshi, Paulsen Martina, Walter Jörn, Reik Wolf, Okumura Katsuzumi
Laboratory of Molecular and Cellular Biology, Faculty of Bioresources, Mie University, Tsu, Japan.
Biosci Biotechnol Biochem. 2002 May;66(5):1046-51. doi: 10.1271/bbb.66.1046.
Genomic imprinting is characterized by allele-specific expression of genes within chromosomal domains. Here we show, using fluorescence in situ hybridization (FISH) analysis, that the large chromosomal domain of the mouse distal chromosome 7 imprinting cluster, approximately 1 Mb in length between p57Kip2 and H19 genes, replicates asynchronously between the two alleles during S-phase. At the telomeric side of this domain, we found a transition from asynchronous replication at the imprinted p57Kip2 gene to synchronous replication at the Nap2 gene. Two-color FISH suggested that the paternal allele of this whole domain replicates earlier than its maternal allele. Treatment of the cells with a histone deacetylase inhibitor abolished this allele-specific feature accompanied with accelerated replication of the later-replicating allele at a domain level. Allele-specific asynchronous replication was observed even in ES cells. These results suggest that this imprinting cluster consists of a large replication domain which is already found at the early stage in development.
基因组印记的特征是染色体区域内基因的等位基因特异性表达。在这里,我们使用荧光原位杂交(FISH)分析表明,小鼠7号染色体远端印记簇的大染色体区域,在p57Kip2和H19基因之间长度约为1 Mb,在S期两个等位基因之间异步复制。在该区域的端粒侧,我们发现从印记的p57Kip2基因处的异步复制到Nap2基因处的同步复制的转变。双色FISH表明该整个区域的父本等位基因比其母本等位基因复制得更早。用组蛋白去乙酰化酶抑制剂处理细胞消除了这种等位基因特异性特征,并伴随着在区域水平上后期复制等位基因的加速复制。即使在胚胎干细胞中也观察到了等位基因特异性异步复制。这些结果表明,这个印记簇由一个在发育早期就已存在的大复制区域组成。