Menne Tobias F, Goyenechea Beatriz, Sánchez-Puig Nuria, Wong Chi C, Tonkin Louise M, Ancliff Philip J, Brost Renée L, Costanzo Michael, Boone Charles, Warren Alan J
Medical Research Council (MRC) Laboratory of Molecular Biology, Hills Road, Cambridge CB2 0QH, UK.
Nat Genet. 2007 Apr;39(4):486-95. doi: 10.1038/ng1994. Epub 2007 Mar 11.
The autosomal recessive disorder Shwachman-Diamond syndrome, characterized by bone marrow failure and leukemia predisposition, is caused by deficiency of the highly conserved Shwachman-Bodian-Diamond syndrome (SBDS) protein. Here, we identify the function of the yeast SBDS ortholog Sdo1, showing that it is critical for the release and recycling of the nucleolar shuttling factor Tif6 from pre-60S ribosomes, a key step in 60S maturation and translational activation of ribosomes. Using genome-wide synthetic genetic array mapping, we identified multiple TIF6 gain-of-function alleles that suppressed the pre-60S nuclear export defects and cytoplasmic mislocalization of Tif6 observed in sdo1Delta cells. Sdo1 appears to function within a pathway containing elongation factor-like 1, and together they control translational activation of ribosomes. Thus, our data link defective late 60S ribosomal subunit maturation to an inherited bone marrow failure syndrome associated with leukemia predisposition.
常染色体隐性疾病施瓦茨曼-戴蒙德综合征的特征为骨髓衰竭和白血病易感性,它是由高度保守的施瓦茨曼-博迪安-戴蒙德综合征(SBDS)蛋白缺乏引起的。在此,我们确定了酵母SBDS直系同源物Sdo1的功能,表明它对于核仁穿梭因子Tif6从60S前体核糖体的释放和再循环至关重要,这是60S成熟和核糖体翻译激活的关键步骤。通过全基因组合成遗传阵列作图,我们鉴定出多个TIF6功能获得性等位基因,这些等位基因抑制了在sdo1Delta细胞中观察到的60S前体核输出缺陷和Tif6的细胞质定位错误。Sdo1似乎在包含延伸因子样1的途径中发挥作用,并且它们共同控制核糖体的翻译激活。因此,我们的数据将有缺陷的60S核糖体亚基后期成熟与一种与白血病易感性相关的遗传性骨髓衰竭综合征联系起来。