Cesare Anthony J, Groff-Vindman Cindy, Compton Sarah A, McEachern Michael J, Griffith Jack D
Corresonding author. Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Mol Cell Biol. 2008 Jan;28(1):20-9. doi: 10.1128/MCB.01122-07. Epub 2007 Oct 29.
The Kluyveromyces lactis ter1-16T strain contains mutant telomeres that are poorly bound by Rap1, resulting in a telomere-uncapping phenotype and significant elongation of the telomeric DNA. The elongated telomeres of ter1-16T allowed the isolation and examination of native yeast telomeric DNA by electron microscopy. In the telomeric DNA isolated from ter1-16T, looped molecules were observed with the physical characteristics of telomere loops (t-loops) previously described in mammalian and plant cells. ter1-16T cells were also found to contain free circular telomeric DNA molecules (t-circles) ranging up to the size of an entire telomere. When the ter1-16T uncapping phenotype was repressed by overexpression of RAP1 or recombination was inhibited by deletion of rad52, the isolated telomeric DNA contained significantly fewer t-loops and t-circles. These results suggest that disruption of Rap1 results in elevated recombination at telomeres, leading to increased strand invasion of the 3' overhang within t-loop junctions and resolution of the t-loop junctions into free t-circles.
乳酸克鲁维酵母ter1-16T菌株含有突变的端粒,这些端粒与Rap1的结合能力较差,导致端粒去帽表型和端粒DNA的显著延长。ter1-16T的延长端粒使得通过电子显微镜对天然酵母端粒DNA进行分离和检测成为可能。在从ter1-16T分离的端粒DNA中,观察到具有先前在哺乳动物和植物细胞中描述的端粒环(t环)物理特征的环状分子。还发现ter1-16T细胞含有大小可达整个端粒的游离环状端粒DNA分子(t环)。当通过RAP1的过表达抑制ter1-16T去帽表型或通过删除rad52抑制重组时,分离的端粒DNA中t环和t环明显减少。这些结果表明,Rap1的破坏导致端粒处的重组增加,导致t环连接处3'突出端的链入侵增加,以及t环连接处分解为游离t环。