Morino Masayuki, Tanaka Miyuki, Shiomi Yasushi, Nishitani Hideo
Graduate School of Life Science, University of Hyogo, Kamigori, Ako-gun, Hyogo, 678-1297, Japan.
Methods Mol Biol. 2014;1170:529-37. doi: 10.1007/978-1-4939-0888-2_29.
S-CDK and DDK protein kinases initiate DNA replication at replication origins. Prior to the activation of these kinases, origins must become competent for replication by loading MCM2-7 DNA helicase on chromatin. This process is known as replication licensing or pre-replicative complex (pre-RC) formation. After the onset of S phase, however, licensing is inhibited to prevent re-replication of DNA. In this chapter, we describe a method to analyze origin licensing by imaging the chromatin-bound licensing factor MCM2-7. In a normal cell cycle, MCM2-7 is loaded at the end of mitosis or early G1 phase. As S phase progresses, MCM2-7 is dissociated from the replicated regions. When DNA replication is completed, cells in G2 phase have no chromatin-bound MCM2-7. The analysis of chromatin-bound MCM2-7 in each cell provides an insight into cell cycle stage and condition for cell cycle.
S-CDK和DDK蛋白激酶在复制起点启动DNA复制。在这些激酶激活之前,复制起点必须通过在染色质上加载MCM2-7解旋酶来具备复制能力。这个过程被称为复制许可或前复制复合体(pre-RC)形成。然而,在S期开始后,许可被抑制以防止DNA重新复制。在本章中,我们描述了一种通过对与染色质结合的许可因子MCM2-7进行成像来分析复制起点许可的方法。在正常细胞周期中,MCM2-7在有丝分裂末期或G1期早期加载。随着S期的进展,MCM2-7从复制区域解离。当DNA复制完成时,G2期细胞没有与染色质结合的MCM2-7。对每个细胞中与染色质结合的MCM2-7进行分析,有助于深入了解细胞周期阶段和细胞周期状况。