MacDougall Christina A, Byun Tony S, Van Christopher, Yee Muh-ching, Cimprich Karlene A
Department of Chemical and Systems Biology, Stanford University, Stanford, California 94305, USA.
Genes Dev. 2007 Apr 15;21(8):898-903. doi: 10.1101/gad.1522607.
Here, we demonstrate that primed, single-stranded DNA (ssDNA) is sufficient for activation of the ATR-dependent checkpoint pathway in Xenopus egg extracts. Using this structure, we define the contribution of the 5'- and 3'-primer ends to Chk1 activation when replication is blocked and ongoing. In addition, we show that although ssDNA is not sufficient for checkpoint activation, the amount of ssDNA adjacent to the primer influences the level of Chk1 phosphorylation. These observations define the minimal DNA requirements for checkpoint activation and suggest that primed ssDNA represents a common checkpoint activating-structure formed following many types of damage.
在此,我们证明了引发的单链DNA(ssDNA)足以在非洲爪蟾卵提取物中激活ATR依赖的检查点通路。利用这种结构,我们确定了在复制受阻和进行过程中5'和3'引物末端对Chk1激活的作用。此外,我们表明,虽然ssDNA不足以激活检查点,但与引物相邻的ssDNA量会影响Chk1磷酸化水平。这些观察结果确定了检查点激活所需的最小DNA条件,并表明引发的ssDNA代表了多种类型损伤后形成的常见检查点激活结构。