Gamble Matthew J, Fisher Robert P
Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, 1275 York Ave., New York, New York 10021, USA.
Nat Struct Mol Biol. 2007 Jun;14(6):548-55. doi: 10.1038/nsmb1248. Epub 2007 May 27.
The histone chaperone SET is required for transcription of chromatin templates by RNA polymerase Pol II (Pol II) in vitro. Here we uncover a positive role for SET in dislodging DEK and PARP1, which restrict access to chromatin in the absence of SET and the PARP1 substrate NAD(+). SET binds chromatin, dissociating DEK and PARP1 to allow transcription in the absence of NAD(+). In the absence of SET, depletion of DEK restores chromatin accessibility to endonuclease but does not permit Mediator recruitment or transcription. In the presence of NAD(+), PARP1 poly(ADP-ribosyl)ates and evicts DEK (and itself) from chromatin to permit Mediator loading and transcription independent of SET. An artificial DEK variant resistant to SET and PARP1 represses transcription, indicating a requirement for DEK removal. Therefore, SET, DEK and PARP1 constitute a network governing access to chromatin by the transcription machinery.
组蛋白伴侣SET在体外RNA聚合酶Pol II(Pol II)转录染色质模板时是必需的。在这里,我们发现SET在去除DEK和PARP1方面具有积极作用,在没有SET和PARP1底物NAD(+)的情况下,DEK和PARP1会限制对染色质的访问。SET与染色质结合,使DEK和PARP1解离,从而在没有NAD(+)的情况下允许转录。在没有SET的情况下,DEK的缺失恢复了染色质对内切核酸酶的可及性,但不允许中介体招募或转录。在有NAD(+)的情况下,PARP1将DEK(以及它自身)聚(ADP-核糖基)化并从染色质上驱逐,以允许中介体加载和独立于SET的转录。一种对SET和PARP1有抗性的人工DEK变体抑制转录,表明需要去除DEK。因此,SET、DEK和PARP1构成了一个控制转录机制对染色质访问的网络。