Nousbeck Janna, Spiegel Ronen, Ishida-Yamamoto Akemi, Indelman Margarita, Shani-Adir Ayelet, Adir Noam, Lipkin Ehud, Bercovici Sivan, Geiger Dan, van Steensel Maurice A, Steijlen Peter M, Bergman Reuven, Bindereif Albrecht, Choder Mordechai, Shalev Stavit, Sprecher Eli
Laboratory of Molecular Dermatology, Department of Dermatology, Rambam Health Care Campus, 31096 Haifa, Israel.
Am J Hum Genet. 2008 May;82(5):1114-21. doi: 10.1016/j.ajhg.2008.03.014. Epub 2008 Apr 24.
Single-gene disorders offer unique opportunities to shed light upon fundamental physiological processes in humans. We investigated an autosomal-recessive phenotype characterized by alopecia, progressive neurological defects, and endocrinopathy (ANE syndrome). By using homozygosity mapping and candidate-gene analysis, we identified a loss-of-function mutation in RBM28, encoding a nucleolar protein. RBM28 yeast ortholog, Nop4p, was previously found to regulate ribosome biogenesis. Accordingly, electron microscopy revealed marked ribosome depletion and structural abnormalities of the rough endoplasmic reticulum in patient cells, ascribing ANE syndrome to the restricted group of inherited disorders associated with ribosomal dysfunction.
单基因疾病为深入了解人类基本生理过程提供了独特机会。我们研究了一种常染色体隐性表型,其特征为脱发、进行性神经缺陷和内分泌病(ANE综合征)。通过纯合子定位和候选基因分析,我们在编码一种核仁蛋白的RBM28中鉴定出一个功能丧失突变。RBM28的酵母直系同源物Nop4p先前被发现可调节核糖体生物合成。相应地,电子显微镜显示患者细胞中核糖体明显减少且粗面内质网结构异常,将ANE综合征归因于与核糖体功能障碍相关的遗传性疾病受限组。