Key Laboratory of Gene Engineering of the Ministry of Education, State Key Laboratory of Oncology in South China, School of Life Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Key Laboratory of Gene Engineering of the Ministry of Education, State Key Laboratory of Oncology in South China, School of Life Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Cell Rep. 2018 Feb 13;22(7):1849-1860. doi: 10.1016/j.celrep.2018.01.057.
Shwachman-Diamond syndrome (SDS) is a rare pediatric disease characterized by various systemic disorders, including hematopoietic dysfunction. The mutation of Shwachman-Bodian-Diamond syndrome (SBDS) gene has been proposed to be a major causative reason for SDS. Although SBDS patients were reported to have shorter telomere length in granulocytes, the underlying mechanism is still unclear. Here we provide data to elucidate the role of SBDS in telomere protection. We demonstrate that SBDS deficiency leads to telomere shortening. We found that overexpression of disease-associated SBDS mutants or knockdown of SBDS hampered the recruitment of telomerase onto telomeres, while the overall reverse transcriptase activity of telomerase remained unaffected. Moreover, we show that SBDS could specifically bind to TPP1 during the S phase of cell cycle, likely functioning as a stabilizer for TPP1-telomerase interaction. Our findings suggest that SBDS is a telomere-protecting protein that participates in regulating telomerase recruitment.
Shwachman-Diamond 综合征(SDS)是一种罕见的儿科疾病,其特征是存在各种全身系统紊乱,包括造血功能障碍。Shwachman-Bodian-Diamond 综合征(SBDS)基因突变被认为是 SDS 的主要致病原因。尽管已有报道称 SBDS 患者的粒细胞中端粒长度较短,但具体的机制仍不清楚。本研究旨在阐明 SBDS 在端粒保护中的作用。结果表明,SBDS 缺乏会导致端粒缩短。我们发现,疾病相关 SBDS 突变体的过表达或 SBDS 的敲低会阻碍端粒酶在端粒上的募集,而端粒酶的整体逆转录酶活性不受影响。此外,我们还表明,SBDS 可以在细胞周期的 S 期特异性结合 TPP1,可能作为 TPP1-端粒酶相互作用的稳定剂。综上,这些发现表明 SBDS 是一种端粒保护蛋白,参与调节端粒酶的募集。