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Kap104p Imports the PY-NLS-containing Transcription Factor Tfg2p into the Nucleus

机译:Kap104p将包含PY-NLS的转录因子Tfg2p导入细胞核

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摘要

A previous bioinformatics study identified a putative PY-NLS in the yeast transcription factor Tfg2p (Suel, K. E., Gu, H., and Chook, Y. M. (2008) PLoS Biol. 6, e137). In this study, we validate Tfg2p as a Kap104p substrate and examine the energetic organization of its PY-NLS. The Tfg2p PY-NLS can target a heterologous protein into the cell nucleus through interactions with Kap104p. Surprisingly, full-length Tfg2p is still localized to the nucleus of Kap104p temperature-sensitive cells and, similarly, Tfg2p with a mutated PY-NLS is nuclear in wild-type cells. Other Karyopherinβs (Kapβs) such as Kap108p and Kap120p also bind Tfg2p and may import it into the nucleus. More importantly, we demonstrate that Tfg2p is retained in the nucleus through DNA binding. Mutations of DNA binding residues relieve nuclear retention and unmask the role of Kap104p in Tfg2p nuclear import. More generally, steady-state localization of a nuclear protein is dictated by its nuclear import and export activities as well as its interactions in the nucleus and the cytoplasm.
机译:先前的生物信息学研究在酵母转录因子Tfg2p中鉴定出推定的PY-NLS(Suel,K.E.,Gu,H.和Chook,Y.M.(2008)PLoS Biol.6,e137)。在这项研究中,我们验证Tfg2p作为Kap104p底物,并检查其PY-NLS的能量结构。 Tfg2p PY-NLS可通过与Kap104p相互作用将异源蛋白靶向细胞核。令人惊讶的是,全长Tfg2p仍然位于Kap104p温度敏感细胞的细胞核中,并且类似地,具有突变的PY-NLS的Tfg2p在野生型细胞中是有核的。其他核转运蛋白β(Kapβs),例如Kap108p和Kap120p也结合Tfg2p,并可能将其导入细胞核。更重要的是,我们证明了Tfg2p通过DNA结合保留在细胞核中。 DNA结合残基的突变缓解了核保留,并揭示了Kap104p在Tfg2p核输入中的作用。更一般地,核蛋白的稳态定位取决于其核的进出口活动及其在核和细胞质中的相互作用。

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