Fulnečková Jana, Ševčíková Tereza, Lukešová Alena, Sýkorová Eva
Institute of Biophysics, Academy of Sciences of the Czech Republic, v.v.i., Královopolská 135, CZ-61265, Brno, Czech Republic.
Faculty of Science, and CEITEC - Central European Institute of Technology, Masaryk University, Kamenice 5, CZ-62500, Brno, Czech Republic.
Chromosoma. 2016 Jun;125(3):437-51. doi: 10.1007/s00412-015-0557-2. Epub 2015 Nov 23.
Telomeres are nucleoprotein structures that distinguish native chromosomal ends from double-stranded breaks. They are maintained by telomerase that adds short G-rich telomeric repeats at chromosomal ends in most eukaryotes and determines the TnAmGo sequence of canonical telomeres. We employed an experimental approach that was based on detection of repeats added by telomerase to identify the telomere sequence type forming the very ends of chromosomes. Our previous studies that focused on the algal order Chlamydomonadales revealed several changes in telomere motifs that were consistent with the phylogeny and supported the concept of the Arabidopsis-type sequence being the ancestral telomeric motif for green algae. In addition to previously described independent transitions to the Chlamydomonas-type sequence, we report that the ancestral telomeric motif was replaced by the human-type sequence in the majority of algal species grouped within a higher order clade, Caudivolvoxa. The Arabidopsis-type sequence was apparently retained in the Polytominia clade. Regarding the telomere sequence, the Chlorogonia clade within Caudivolvoxa bifurcates into two groups, one with the human-type sequence and the other group with the Arabidopsis-type sequence that is solely formed by the Chlorogonium species. This suggests that reversion to the Arabidopsis-type telomeric motif occurred in the common ancestral Chlorogonium species. The human-type sequence is also synthesized by telomerases of algal strains from Arenicolinia, Dunaliellinia and Stephanosphaerinia, except a distinct subclade within Stephanosphaerinia, where telomerase activity was not detected and a change to an unidentified telomeric motif might arise. We discuss plausible reasons why changes in telomeric motifs were tolerated during evolution of green algae.
端粒是一种核蛋白结构,可将天然染色体末端与双链断裂区分开来。在大多数真核生物中,端粒由端粒酶维持,端粒酶在染色体末端添加富含鸟嘌呤的短端粒重复序列,并决定了标准端粒的TnAmGo序列。我们采用了一种基于检测端粒酶添加的重复序列的实验方法,以鉴定构成染色体末端的端粒序列类型。我们之前专注于绿藻目(Chlamydomonadales)的研究揭示了端粒基序的几种变化,这些变化与系统发育一致,并支持拟南芥型序列是绿藻祖先端粒基序的概念。除了先前描述的向衣藻型序列的独立转变外,我们报告在一个更高阶的进化枝Caudivolvoxa中的大多数藻类物种中,祖先端粒基序被人类型序列所取代。拟南芥型序列显然保留在Polytominia进化枝中。关于端粒序列,Caudivolvoxa中的Chlorogonia进化枝分为两组,一组具有人类型序列,另一组仅由Chlorogonium物种形成的具有拟南芥型序列。这表明在共同的祖先Chlorogonium物种中发生了向拟南芥型端粒基序的逆转。来自Arenicolinia、Dunaliellinia和Stephanosphaerinia的藻类菌株的端粒酶也合成人类型序列,但Stephanosphaerinia内的一个独特亚分支除外,在该亚分支中未检测到端粒酶活性,可能会出现向未鉴定的端粒基序的变化。我们讨论了在绿藻进化过程中端粒基序变化被容忍的合理原因。