Suppr超能文献

主要酵母多药耐药(MDR)转录因子Pdr1的Pse1/Kap121依赖性核定位

Pse1/Kap121-dependent nuclear localization of the major yeast multidrug resistance (MDR) transcription factor Pdr1.

作者信息

Delahodde A, Pandjaitan R, Corral-Debrinski M, Jacq C

机构信息

Laboratoire de Génétique Moléculaire, CNRS, UMR 8541, Ecole Normale Supérieure, 46 rue d'Ulm, 75230 Paris Cedex 05, France.

出版信息

Mol Microbiol. 2001 Jan;39(2):304-12. doi: 10.1046/j.1365-2958.2001.02182.x.

Abstract

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.

摘要

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。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验