Andreassen P R, Lacroix F B, Margolis R L
Institut de Biologie Structurale Jean-Pierre Ebel (CEA/CNRS), Grenoble, France.
J Cell Biol. 1997 Jan 13;136(1):29-43. doi: 10.1083/jcb.136.1.29.
Here we report that DNA decatenation is not a physical requirement for the formation of mammalian chromosomes containing a two-armed chromosome scaffold. 2-aminopurine override of G2 arrest imposed by VM-26 or ICRF-193, which inhibit topoisomerase II (topo II)-dependent DNA decatenation, results in the activation of p34cdc2 kinase and entry into mitosis. After override of a VM-26-dependent checkpoint, morphologically normal compact chromosomes form with paired axial cores containing topo II and ScII. Despite its capacity to form chromosomes of normal appearance, the chromatin remains covalently complexed with topo II at continuous levels during G2 arrest with VM-26. Override of an ICRF-193 block, which inhibits topo II-dependent decatenation at an earlier step than VM-26, also generates chromosomes with two distinct, but elongated, parallel arms containing topo II and ScII. These data demonstrate that DNA decatenation is required to pass a G2 checkpoint, but not to restructure chromatin for chromosome formation. We propose that the chromosome core structure is templated during interphase, before DNA decatenation, and that condensation of the two-armed chromosome scaffold can therefore occur independently of the formation of two intact and separate DNA helices.
我们在此报告,DNA解连环对于含有双臂染色体支架的哺乳动物染色体形成并非物理上的必需条件。由VM - 26或ICRF - 193(它们抑制拓扑异构酶II(topo II)依赖性DNA解连环)所施加的G2期阻滞可被2 - 氨基嘌呤克服,这会导致p34cdc2激酶激活并进入有丝分裂。在克服了依赖VM - 26的检查点后,形态正常的致密染色体形成,带有包含topo II和ScII的成对轴向核心。尽管有能力形成外观正常的染色体,但在用VM - 26进行G2期阻滞期间,染色质仍与topo II持续共价结合。ICRF - 193阻滞比VM - 26在更早步骤抑制topo II依赖性解连环,克服该阻滞也会产生具有两条不同但伸长的平行臂且包含topo II和ScII的染色体。这些数据表明,DNA解连环是通过G2检查点所必需的,但并非是为染色体形成而重塑染色质所必需的。我们提出,染色体核心结构在间期DNA解连环之前就已形成模板,因此双臂染色体支架的凝聚可以独立于两条完整且分开的DNA螺旋的形成而发生。