Lei Elissa P, Stern Charlene A, Fahrenkrog Birthe, Krebber Heike, Moy Terence I, Aebi Ueli, Silver Pamela A
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School and Dana Farber Cancer Institute, Boston, Massachusetts 02115, USA.
Mol Biol Cell. 2003 Mar;14(3):836-47. doi: 10.1091/mbc.e02-08-0520.
In eukaryotes, mRNAs are transcribed in the nucleus and exported to the cytoplasm for translation to occur. Messenger RNAs complexed with proteins referred to as ribonucleoparticles are recognized for nuclear export in part by association with Mex67, a key Saccharomyces cerevisiae mRNA export factor and homolog of human TAP/NXF1. Mex67, along with its cofactor Mtr2, is thought to promote ribonucleoparticle translocation by interacting directly with components of the nuclear pore complex (NPC). Herein, we show that the nuclear pore-associated protein Sac3 functions in mRNA export. Using a mutant allele of MTR2 as a starting point, we have identified a mutation in SAC3 in a screen for synthetic lethal interactors. Loss of function of SAC3 causes a strong nuclear accumulation of mRNA and synthetic lethality with a number of mRNA export mutants. Furthermore, Sac3 can be coimmunoprecipitated with Mex67, Mtr2, and other factors involved in mRNA export. Immunoelectron microscopy analysis shows that Sac3 localizes exclusively to cytoplasmic fibrils of the NPC. Finally, Mex67 accumulates at the nuclear rim when SAC3 is mutated, suggesting that Sac3 functions in Mex67 translocation through the NPC.
在真核生物中,mRNA在细胞核内转录,然后输出到细胞质中进行翻译。与称为核糖核蛋白颗粒的蛋白质复合的信使RNA,部分通过与Mex67结合而被识别用于核输出,Mex67是酿酒酵母中一种关键的mRNA输出因子,也是人类TAP/NXF1的同源物。Mex67与其辅因子Mtr2一起,被认为通过直接与核孔复合体(NPC)的成分相互作用来促进核糖核蛋白颗粒的转运。在此,我们表明核孔相关蛋白Sac3在mRNA输出中起作用。以MTR2的一个突变等位基因为起点,我们在合成致死相互作用因子的筛选中鉴定出SAC3中的一个突变。Sac3功能缺失会导致mRNA在细胞核中大量积累,并与许多mRNA输出突变体产生合成致死性。此外,Sac3可以与Mex67、Mtr2以及其他参与mRNA输出的因子进行共免疫沉淀。免疫电子显微镜分析表明,Sac3仅定位于NPC的细胞质纤维。最后,当SAC3发生突变时,Mex67会在核边缘积累,这表明Sac3在Mex67通过NPC的转运中起作用。