Panzeri L, Landonio L, Stotz A, Philippsen P
EMBO J. 1985 Jul;4(7):1867-74. doi: 10.1002/j.1460-2075.1985.tb03862.x.
Conserved sequence features in Saccharomyces cerevisiae CEN DNA are confined to a region of approximately 120 bp. The highly conserved 8 bp at the left (PuTCACPuTG) constitute the left boundary of a functional CEN DNA as shown by the analysis of a series of Bal31 deletions. The right boundary of a functional CEN DNA lies within the conserved 25 bp at the right (TGT-T-TG--TTCCGAA-----AAA) or a few base pairs further outside of the 120-bp region. One mutant which just lacks the left conserved DNA element PuTCACPuTG can still assemble into a partially functional mitotic centromere and it assembles into a well functioning meiotic centromere. The sequences between the two conserved terminal DNA elements can be increased in length (+50%) or in GC content (from 6% to 12%) without measurable changes in mitotic and meiotic segregations of plasmids carrying such CEN mutations. The naturally occurring length and GC content of this centromere DNA sequence element is, therefore, not essential for centromere function. We discuss the possibility that it partly acts as a hinge region between two domains. Finally, we tested integrations of CEN DNA into the genome and found a toleration of wild-type CEN6 DNA when present 3' of the LYS2 gene.
酿酒酵母着丝粒DNA中的保守序列特征局限于大约120 bp的区域。如对一系列Bal31缺失的分析所示,左侧高度保守的8 bp(PuTCACPuTG)构成了功能性着丝粒DNA的左边界。功能性着丝粒DNA的右边界位于右侧保守的25 bp(TGT-T-TG--TTCCGAA-----AAA)内或120 bp区域之外的几个碱基对处。一个仅缺少左侧保守DNA元件PuTCACPuTG的突变体仍可组装成部分功能性的有丝分裂着丝粒,并且能组装成功能良好的减数分裂着丝粒。携带此类着丝粒突变的质粒在有丝分裂和减数分裂分离过程中,两个保守末端DNA元件之间的序列长度可增加(+50%)或GC含量可增加(从6%到12%),而无明显变化。因此,这种着丝粒DNA序列元件的天然长度和GC含量对着丝粒功能并非必需。我们讨论了它部分作为两个结构域之间铰链区域的可能性。最后,我们测试了着丝粒DNA整合到基因组中的情况,发现当野生型CEN6 DNA存在于LYS2基因的3'端时可被容忍。