Quantitative Proteomics, Institute of Molecular Biology, 55128 Mainz, Germany.
Hefei National Laboratory for Physical Sciences at Microscale and School of Life Sciences, University of Science and Technology of China, 230027 Hefei, Anhui, China.
Nucleic Acids Res. 2019 Feb 28;47(4):1896-1907. doi: 10.1093/nar/gky1289.
Telomeres are nucleoprotein structures at the ends of linear chromosomes and present an essential feature for genome integrity. Vertebrate telomeres usually consist of hexameric TTAGGG repeats, however, in cells that use the alternative lengthening of telomeres (ALT) mechanism, variant repeat sequences are interspersed throughout telomeres. Previously, it was shown that NR2C/F transcription factors bind to TCAGGG variant repeats and contribute to telomere maintenance in ALT cells. While specific binders to other variant repeat sequences have been lacking to date, we here identify ZBTB10 as the first TTGGGG-binding protein and demonstrate direct binding via the two zinc fingers with affinity in the nanomolar range. Concomitantly, ZBTB10 co-localizes with a subset of telomeres in ALT-positive U2OS cells and interacts with TRF2/RAP1 via the N-terminal region of TRF2. Our data establishes ZBTB10 as a novel variant repeat binding protein at ALT telomeres.
端粒是线性染色体末端的核蛋白结构,是基因组完整性的重要特征。脊椎动物端粒通常由六聚体 TTAGGG 重复序列组成,然而,在使用端粒的替代延长(ALT)机制的细胞中,变体重复序列散布在整个端粒中。以前已经表明,NR2C/F 转录因子与 TCAGGG 变体重复序列结合,并有助于 ALT 细胞中端粒的维持。虽然迄今为止还缺乏其他变体重复序列的特异性结合物,但我们在这里确定 ZBTB10 是第一个 TTGGGG 结合蛋白,并通过两个锌指以纳摩尔范围的亲和力证明了直接结合。同时,ZBTB10 在 ALT 阳性 U2OS 细胞中与一部分端粒共定位,并通过 TRF2 的 N 端与 TRF2/RAP1 相互作用。我们的数据确立了 ZBTB10 作为 ALT 端粒上的新型变体重复结合蛋白。