INSERM U768, Paris, France.
Hum Mol Genet. 2013 Aug 15;22(16):3239-49. doi: 10.1093/hmg/ddt178. Epub 2013 Apr 15.
Hoyeraal-Hreidarsson syndrome (HHS), a severe variant of dyskeratosis congenita (DC), is characterized by early onset bone marrow failure, immunodeficiency and developmental defects. Several factors involved in telomere length maintenance and/or protection are defective in HHS/DC, underlining the relationship between telomere dysfunction and these diseases. By combining whole-genome linkage analysis and exome sequencing, we identified compound heterozygous RTEL1 (regulator of telomere elongation helicase 1) mutations in three patients with HHS from two unrelated families. RTEL1 is a DNA helicase that participates in DNA replication, DNA repair and telomere integrity. We show that, in addition to short telomeres, RTEL1-deficient cells from patients exhibit hallmarks of genome instability, including spontaneous DNA damage, anaphase bridges and telomeric aberrations. Collectively, these results identify RTEL1 as a novel HHS-causing gene and highlight its role as a genomic caretaker in humans.
Hoyeraal-Hreidarsson 综合征(HHS)是先天性角化不良(DC)的一种严重变异,其特征为早期骨髓衰竭、免疫缺陷和发育缺陷。HHS/DC 中涉及端粒长度维持和/或保护的几个因素存在缺陷,这突显了端粒功能障碍与这些疾病之间的关系。通过全基因组连锁分析和外显子组测序,我们在两个无关联家族的 3 名 HHS 患者中鉴定出复合杂合的 RTEL1(端粒延长解旋酶 1 调节因子)突变。RTEL1 是一种参与 DNA 复制、DNA 修复和端粒完整性的 DNA 解旋酶。我们表明,除了端粒较短之外,来自患者的 RTEL1 缺陷细胞还表现出基因组不稳定性的特征,包括自发的 DNA 损伤、后期桥和端粒异常。总的来说,这些结果将 RTEL1 确定为一种新的 HHS 致病基因,并强调了它在人类中作为基因组守护者的作用。