Derboven Elisa, Ekker Heinz, Kusenda Branislav, Bulankova Petra, Riha Karel
Gregor Mendel Institute, Austrian Academy of Sciences, Vienna, Austria.
Campus Science Support Facilities, Next Generation Sequencing Facility, Vienna, Austria.
PLoS Genet. 2014 Oct 9;10(10):e1004682. doi: 10.1371/journal.pgen.1004682. eCollection 2014 Oct.
The CST (Cdc13/CTC1-STN1-TEN1) complex was proposed to have evolved kingdom specific roles in telomere capping and replication. To shed light on its evolutionary conserved function, we examined the effect of STN1 dysfunction on telomere structure in plants. STN1 inactivation in Arabidopsis leads to a progressive loss of telomeric DNA and the onset of telomeric defects depends on the initial telomere size. While EXO1 aggravates defects associated with STN1 dysfunction, it does not contribute to the formation of long G-overhangs. Instead, these G-overhangs arise, at least partially, from telomerase-mediated telomere extension indicating a deficiency in C-strand fill-in synthesis. Analysis of hypomorphic DNA polymerase α mutants revealed that the impaired function of a general replication factor mimics the telomeric defects associated with CST dysfunction. Furthermore, we show that STN1-deficiency hinders re-replication of heterochromatic regions to a similar extent as polymerase α mutations. This comparative analysis of stn1 and pol α mutants suggests that STN1 plays a genome-wide role in DNA replication and that chromosome-end deprotection in stn1 mutants may represent a manifestation of aberrant replication through telomeres.
CST(Cdc13/CTC1-STN1-TEN1)复合体被认为在端粒封端和复制过程中具有特定于不同生物界的进化作用。为了阐明其进化上保守的功能,我们研究了STN1功能障碍对植物端粒结构的影响。拟南芥中STN1失活会导致端粒DNA逐渐丢失,端粒缺陷的出现取决于初始端粒大小。虽然EXO1会加剧与STN1功能障碍相关的缺陷,但它对长G链悬突的形成没有作用。相反,这些G链悬突至少部分源自端粒酶介导的端粒延伸,表明C链填补合成存在缺陷。对低表达DNA聚合酶α突变体的分析表明,一种一般复制因子功能受损会模拟与CST功能障碍相关的端粒缺陷。此外,我们发现STN1缺陷对异染色质区域再复制的阻碍程度与聚合酶α突变相似。对stn1和pol α突变体的这种比较分析表明,STN1在全基因组DNA复制中发挥作用,并且stn1突变体中的染色体末端去保护可能代表了通过端粒的异常复制的一种表现。