The cytosolic iron-sulfur cluster assembly (CIA) system biosynthesizes iron-sulfur (FeS) cluster cofactors for cytosolic and nuclear proteins. The yeast Cia2 protein is the central component of the targeting complex which identifes apo-protein targets in the final step of the pathway. Herein, we determine that Cia2 contains five conserved motifs distributed between an intrinsically disordered N-terminal domain and a C-terminal domain of unknown function 59 (DUF59). The disordered domain is dispensible for binding the other subunits of the targeting complex, Met18 and Cia1, and the apo-target Rad3 in vitro. While in vivo assays reveal that the C-terminal domain is sufficient to support viability, several phenotypic assays indicate that deletion of the N-terminal domain negatively impacts CIA function. We additionally establish that Glu208, located within a conserved motif found only in eukaryotic DUF59 proteins, is important for the Cia1-Cia2 interaction in vitro. In vivo, E208A-Cia2 results in a diminished activity of the cytosolic iron sulfur cluster protein, Leu1 but only modest effects on hydroxyurea or methylmethane sulfonate sensitivity. Finally, we demonstrate that neither of the two highly conserved motifs of the DUF59 domain are vital for any of Cia2’s interactions in vitro yet mutation of the DPE motif in the DUF59 domain results in a nonfunctional allele in vivo. Our observation that four of the five highly conserved motifs of Cia2 are dispensable for targeting complex formation and apo-target binding suggests that Cia2 is not simply a protein-protein interaction mediator but it likely possesses an additional, currently cryptic, function during the final cluster insertion step of CIA.

中文翻译：

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定义Cia2在体内和体外的基本功能所需的域

胞质铁硫簇装配（CIA）系统生物合成胞质和核蛋白的铁硫（FeS）簇辅因子。酵母Cia2蛋白是靶向复合物的主要成分，该复合物在通路的最后一步识别脱辅基蛋白靶标。在本文中，我们确定Cia2包含五个保守的基序，分布在本质上无序的N末端结构域和未知功能59（DUF59）的C末端结构域之间。在体外，无序域对于结合靶向复合物的其他亚基Met18和Cia1和载脂蛋白靶Rad3是必不可少的。尽管体内测定显示C末端结构域足以支持生存能力，但一些表型测定表明N末端结构域的缺失会对CIA功能产生负面影响。我们还建立了Glu208，位于仅在真核DUF59蛋白中发现的保守基序内，对于Cia1-Cia2体外相互作用很重要。在体内，E208A-Cia2导致胞质铁硫簇蛋白Leu1的活性减弱，但对羟基脲或甲基甲烷磺酸盐敏感性的影响很小。最后，我们证明了DUF59域的两个高度保守的基序对于任何Cia2的体外相互作用都不是至关重要的，但DUF59域中DPE基序的突变导致体内无功能的等位基因。我们的观察结果表明，Cia2的五个高度保守的基序中有四个对于靶向复合物形成和载脂蛋白-靶标结合而言是可有可无的，这表明Cia2不仅是蛋白质-蛋白质相互作用的介体，而且还可能具有另外一个（目前是隐秘的）