van Brabant A J, Fangman W L, Brewer B J
Department of Genetics, University of Washington, Seattle, Washington 98195-7360, USA.
Mol Cell Biol. 1999 Jun;19(6):4231-40. doi: 10.1128/MCB.19.6.4231.
Yeast artificial chromosomes (YACs) are a common tool for cloning eukaryotic DNA. The manner by which large pieces of foreign DNA are assimilated by yeast cells into a functional chromosome is poorly understood, as is the reason why some of them are stably maintained and some are not. We examined the replication of a stable YAC containing a 240-kb insert of DNA from the human T-cell receptor beta locus. The human insert contains multiple sites that serve as origins of replication. The activity of these origins appears to require the yeast ARS consensus sequence and, as with yeast origins, additional flanking sequences. In addition, the origins in the human insert exhibit a spacing, a range of activation efficiencies, and a variation in times of activation during S phase similar to those found for normal yeast chromosomes. We propose that an appropriate combination of replication origin density, activation times, and initiation efficiencies is necessary for the successful maintenance of YAC inserts.
酵母人工染色体(YACs)是克隆真核生物DNA的常用工具。酵母细胞将大片段外源DNA整合到功能性染色体中的方式尚不清楚,同样不清楚的是为什么有些能稳定维持而有些不能。我们研究了一个稳定的YAC的复制情况,该YAC含有来自人类T细胞受体β基因座的240 kb DNA插入片段。人类插入片段包含多个作为复制起点的位点。这些起点的活性似乎需要酵母ARS共有序列,并且与酵母起点一样,还需要额外的侧翼序列。此外,人类插入片段中的起点在S期表现出间隔、一系列激活效率以及激活时间的变化,类似于正常酵母染色体中的情况。我们提出,复制起点密度、激活时间和起始效率的适当组合对于YAC插入片段的成功维持是必要的。