Zhang Haitao, Audry Julien, Runge Kurt W
Inflammation and Immunity, Cleveland Clinic Lerner Research Institute, Cleveland, OH USA.
MicroPubl Biol. 2025 May 30;2025. doi: 10.17912/micropub.biology.001622. eCollection 2025.
We have formed new short telomeres in using an inducible nuclease that cuts near telomere repeats in cells that lack, cannot recruit or cannot fully activate telomerase. Sequencing these new telomeres showed that cells can divide at least 4 times with ~30 bp of non-telomeric sequence at the chromosome end in cells lacking telomerase, which contrasts with current models for the roles of terminal single-stranded telomere repeats and the telomere proteins in telomere protection and replication. Cells that cannot recruit or activate telomerase had similar results, with additional terminal truncations or telomere repeat addition.
我们利用一种可诱导的核酸酶在缺乏、无法招募或无法完全激活端粒酶的细胞中,在靠近端粒重复序列处进行切割,从而形成了新的短端粒。对这些新端粒进行测序表明,在缺乏端粒酶的细胞中,染色体末端带有约30个碱基对的非端粒序列时,细胞至少可以分裂4次,这与目前关于末端单链端粒重复序列和端粒蛋白在端粒保护和复制中作用的模型形成对比。无法招募或激活端粒酶的细胞也有类似结果,伴有额外的末端截短或端粒重复序列添加。