Okuno Y, Satoh H, Sekiguchi M, Masukata H
Department of Biology, Graduate School of Science, Osaka University, Toyonaka, Japan.
Mol Cell Biol. 1999 Oct;19(10):6699-709. doi: 10.1128/MCB.19.10.6699.
We have determined functional elements required for autonomous replication of the Schizosaccharomyces pombe ars2004 that acts as an intrinsic chromosomal replication origin. Internal deletion analysis of a 940-bp fragment (ars2004M) showed three regions, I to III, to be required for autonomously replicating sequence (ARS) activity. Eight-base-pair substitutions in the 40-bp region I, composed of arrays of adenines on a DNA strand, resulted in a great reduction of ARS activity. Substitutions of region I with synthetic sequences showed that no specific sequence but rather repeats of three or more consecutive adenines or thymines, without interruption by guanine or cytosine, are required for the ARS activity. The 65-bp region III contains 11 repeats of the AAAAT sequence, while the 165-bp region II has short adenine or thymine stretches and a guanine- and cytosine-rich region which enhances ARS activity. All three regions in ars2004M can be replaced with 40-bp poly(dA/dT) fragments without reduction of ARS activity. Although spacer regions in the ars2004M enhance ARS activity, all could be deleted when an 40-bp poly(dA/dT) fragment was added in place of region I. Our results suggest that the origin activity of fission yeast replicators depends on the number of adenine/thymine stretches, the extent of their clustering, and presence of certain replication-enhancing elements.
我们已经确定了粟酒裂殖酵母ars2004自主复制所需的功能元件,该元件作为一个内在的染色体复制起点。对一个940 bp片段(ars2004M)进行内部缺失分析,结果显示有三个区域(I至III)对于自主复制序列(ARS)活性是必需的。在由DNA链上的腺嘌呤阵列组成的40 bp区域I中进行8个碱基对的替换,导致ARS活性大幅降低。用合成序列替换区域I的结果表明,对于ARS活性而言,不需要特定序列,而是需要三个或更多连续腺嘌呤或胸腺嘧啶的重复,且中间不被鸟嘌呤或胞嘧啶打断。65 bp的区域III包含11个AAAAT序列的重复,而165 bp的区域II有短的腺嘌呤或胸腺嘧啶片段以及一个富含鸟嘌呤和胞嘧啶的区域,该区域可增强ARS活性。ars2004M中的所有三个区域都可以被40 bp的聚(dA/dT)片段替换,而不会降低ARS活性。尽管ars2004M中的间隔区域可增强ARS活性,但当添加一个40 bp的聚(dA/dT)片段来替代区域I时,所有间隔区域都可以被删除。我们的结果表明,裂殖酵母复制子的起点活性取决于腺嘌呤/胸腺嘧啶片段的数量、它们的聚集程度以及某些复制增强元件的存在。