Bednenko J, Melek M, Greene E C, Shippen D E
Department of Biochemistry and Biophysics, Texas A&M University, College Station 77843-2128, USA.
EMBO J. 1997 May 1;16(9):2507-18. doi: 10.1093/emboj/16.9.2507.
Telomerase serves a dual role at telomeres, maintaining tracts of telomere repeats and forming telomeres de novo on broken chromosomes in a process called chromosome healing. In ciliates, both mechanisms are readily observed. Vegetatively growing cells maintain pre-existing telomeres, while cells undergoing macronuclear development fragment their chromosomes and form telomeres de novo. Here we provide the first evidence for developmentally regulated initiation of DNA synthesis by telomerase. In vitro assays were conducted with telomerase from vegetative and developing Euplotes macronuclei using chimeric primers that contained non-telomeric 3' ends and an upstream stretch of telomeric DNA. In developing macronuclei, chimeric primers had two fates: nucleotides were either polymerized directly onto the 3' terminus or residues were removed from the 3' end by endonucleolytic cleavage before polymerization began. In contrast, telomerase from vegetative macronuclei used only the cleavage pathway. Telomere repeat addition onto non-telomeric 3' ends was lost when developing macronuclei were lysed and the contents purified on glycerol gradients. However, when fractions from the glycerol gradient were added back to partially purified telomerase, telomere synthesis was restored. The data indicate that a dissociable chromosome healing factor (CHF) collaborates with telomerase to initiate developmentally programmed de novo telomere formation.
端粒酶在端粒发挥双重作用,维持端粒重复序列的片段,并在一个称为染色体修复的过程中在断裂的染色体上重新形成端粒。在纤毛虫中,这两种机制都很容易观察到。营养生长的细胞维持预先存在的端粒,而经历大核发育的细胞则使它们的染色体断裂并重新形成端粒。在这里,我们提供了端粒酶在发育过程中调控DNA合成起始的首个证据。使用包含非端粒3'末端和一段上游端粒DNA的嵌合引物,对来自营养型和发育型大核的游仆虫端粒酶进行了体外测定。在发育中的大核中,嵌合引物有两种命运:核苷酸要么直接聚合到3'末端,要么在聚合开始前通过内切核酸酶切割从3'末端去除残基。相比之下,来自营养型大核的端粒酶仅使用切割途径。当发育中的大核被裂解并在甘油梯度上纯化其内容物时,端粒重复序列添加到非端粒3'末端的过程就会消失。然而,当将甘油梯度中的组分重新添加到部分纯化的端粒酶中时,端粒合成得以恢复。数据表明,一种可解离的染色体修复因子(CHF)与端粒酶协同作用,启动发育程序控制的端粒从头形成。