Bednenko J, Melek M, Shippen D E
Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843-2128, USA.
Nucleic Acids Res. 1998 Sep 1;26(17):3998-4004. doi: 10.1093/nar/26.17.3998.
Telomerase from the ciliate Euplotes crassus incorporates G4T4telomeric repeats onto both telomeric and non-telomeric single-stranded DNA 3'-ends via reverse transcription of a templating domain in its RNA subunit. Here we describe an unusual mode of template copying that is characteristic of DNA synthesis onto non-telomeric 3'-ends in vitro . When dTTP was eliminated from telomerase reactions, telomeric primers or DNA products generated from the telomerase endonuclease were extended by precise copying of the RNA template. In contrast, telomerase catalyzed the addition of up to 13 dG residues onto primers with non-telomeric 3'-ends under the same reaction conditions. Introducing mismatches in the 3'-terminus of telomeric primers that reduced primer complementarity to the RNA template induced reiterative dG incorporation, indicating that the reaction is influenced by Watson-Crick base pair formation between the primer and the RNA template. Unexpectedly, the reiterative dG addition mode was confined to telomerase derived from developing cells that undergo new telomere formation. This reaction was not observed in vegetatively growing cells. We postulate that indiscriminate dG addition by telomerase occurs by reiterative copying of C residues in the telomerase RNA templating domain and reflects lateral instability of the primer-template interaction during de novo telomere formation.
来自纤毛虫类粗尾真核生物的端粒酶通过逆转录其RNA亚基中的模板结构域,将G4T4端粒重复序列整合到端粒和非端粒单链DNA的3'-末端。在这里,我们描述了一种不寻常的模板复制模式,这是体外DNA合成到非端粒3'-末端的特征。当从端粒酶反应中去除dTTP时,端粒引物或由端粒酶内切核酸酶产生的DNA产物通过精确复制RNA模板而延伸。相反,在相同反应条件下,端粒酶催化在具有非端粒3'-末端的引物上添加多达13个dG残基。在端粒引物的3'-末端引入错配,降低引物与RNA模板的互补性,会诱导重复性dG掺入,这表明该反应受引物与RNA模板之间的沃森-克里克碱基对形成的影响。出乎意料的是,重复性dG添加模式仅限于来自经历新端粒形成的发育细胞的端粒酶。在营养生长的细胞中未观察到这种反应。我们推测,端粒酶不加选择地添加dG是通过重复复制端粒酶RNA模板结构域中的C残基发生的,并且反映了从头端粒形成过程中引物-模板相互作用的侧向不稳定性。