Delahodde A, Pandjaitan R, Corral-Debrinski M, Jacq C
Laboratoire de Génétique Moléculaire, CNRS, UMR 8541, Ecole Normale Supérieure, 46 rue d'Ulm, 75230 Paris Cedex 05, France.
Mol Microbiol. 2001 Jan;39(2):304-12. doi: 10.1046/j.1365-2958.2001.02182.x.
Pdr1 and Pdr3 are two very similar transcription factors that mainly control membrane biogenesis by adjusting the production of different membrane proteins, such as different ABC or major facilitator superfamily (MFS) transporters. We observed that the pse1-1 mutation in the importin/beta-karyopherin Pse1/Kap121 specifically induced the cytoplasmic localization of Pdr1, but not that of Pdr3. Interactions between Pse1 and Pdr1 could be observed in vivo, and a short peptide of 44 amino acids from Pdr1 was shown to contain the information necessary and sufficient for Pse1-dependent nuclear import. This Pdr1-NLS sequence, absent in Pdr3, although rich in serine and tyrosine, is different from the Pse1-dependent nuclear localization signal (NLS) of Pho4. Furthermore, we showed that Pse1/Kap121 is likely to be the sole import receptor for the regulator Pdr1. Together, these new observations underscore the diversity of cellular processes that address to the nucleus two very similar transcription factors involved in the control of the same phenotype, thus securing their function in the cell.
Pdr1和Pdr3是两个非常相似的转录因子,主要通过调节不同膜蛋白的产生来控制膜生物合成,例如不同的ABC转运蛋白或主要易化子超家族(MFS)转运蛋白。我们观察到,输入蛋白/β-核转运蛋白Pse1/Kap121中的pse1-1突变特异性地诱导了Pdr1的细胞质定位,但未诱导Pdr3的细胞质定位。在体内可以观察到Pse1与Pdr1之间的相互作用,并且来自Pdr1的一段44个氨基酸的短肽被证明包含Pse1依赖性核输入所需和足够的信息。Pdr3中不存在这种Pdr1-NLS序列,尽管富含丝氨酸和酪氨酸,但它与Pho4的Pse1依赖性核定位信号(NLS)不同。此外,我们表明Pse1/Kap121可能是调节因子Pdr1的唯一输入受体。总之,这些新观察结果强调了细胞过程的多样性,这些过程将两个参与控制相同表型的非常相似的转录因子输送到细胞核,从而确保它们在细胞中的功能。