Fisher Daniel, Méchali Marcel
Institute of Human Genetics, CNRS, 141 rue de la Cardonille, 34396 Cedex 05 Montpellier, France.
EMBO J. 2003 Jul 15;22(14):3737-48. doi: 10.1093/emboj/cdg352.
To study the relationship between DNA replication and transcription in vivo, we investigated Hox gene activation in two vertebrate systems: the embryogenesis of Xenopus and the retinoic acid-induced differentiation of pluripotent mouse P19 cells. We show that the first cell cycles following the mid- blastula transition in Xenopus are necessary and sufficient for HoxB activation, whereas later cell cycles are necessary for the correct expression pattern. In P19 cells, HoxB expression requires proliferation, and the entire locus is activated within one cell cycle. Using synchronous cultures, we found that activation of HoxB genes is colinear within a single cell cycle, occurs during S phase and requires S phase. The HoxB locus replicates early, whereas replication is still required for maximal expression later in S phase. Thus, induction of HoxB genes occurs in a DNA replication-dependent manner and requires only one cell cycle. We propose that S-phase remodelling licenses the locus for transcriptional regulation.
为了研究体内DNA复制与转录之间的关系,我们在两个脊椎动物系统中研究了Hox基因的激活:非洲爪蟾的胚胎发生以及视黄酸诱导的多能小鼠P19细胞的分化。我们发现,非洲爪蟾囊胚中期转变后的最初几个细胞周期对于HoxB的激活是必要且充分的,而随后的细胞周期对于正确的表达模式是必要的。在P19细胞中,HoxB的表达需要增殖,并且整个基因座在一个细胞周期内被激活。使用同步培养,我们发现HoxB基因的激活在单个细胞周期内是共线性的,发生在S期并且需要S期。HoxB基因座早期复制,而在S期后期仍需要复制以实现最大表达。因此,HoxB基因的诱导以DNA复制依赖的方式发生,并且只需要一个细胞周期。我们提出,S期重塑为转录调控许可了该基因座。