Baños-Jaime Blanca, Uceda-Mayo Ana B, Rivero-Rodríguez Francisco, Casado-Combreras Miguel Á, Velázquez-Cruz Alejandro, Velázquez-Campoy Adrián, Corrales-Guerrero Laura, De la Rosa Miguel A, Díaz-Moreno Irene
Institute for Chemical Research (IIQ), Scientific Research Center "Isla de la Cartuja" (cicCartuja), University of Seville-CSIC, Avda. Americo Vespucio 49, Seville, 41092, Spain.
Institute for Biocomputation and Physic of Complex Systems (BIFI), Joint Unit GBsC-CSIC-BIFI, University of Zaragoza, C. Mariano Esquillor, Zaragoza, 50018, Spain.
Adv Sci (Weinh). 2025 Mar;12(12):e2415566. doi: 10.1002/advs.202415566. Epub 2025 Jan 31.
Gene duplication has allowed protein evolution toward novel functions and mechanisms. The differences between paralogous genes frequently rely on the sequence of disordered regions. For instance, in mammals, the chaperones ANP32A and ANP32B share a common evolutionary line and have some exchangeable functions based on their similar N-terminal domains. Nevertheless, their C-terminal low-complexity-acidic-regions (LCARs) display substantial sequence differences, unveiling some degree of variability between them, in agreement with their different tissue-specific expression patterns. These structural and computational results indicate that a substitution in the vicinity of the nuclear localization signal (NLS), of Pro in ANP32A for Thr in ANP32B, determines the overall compactness of the C-terminal LCAR. The different structural properties of the disordered region affect the binding mode of ANP32 members to their targets. This type of divergent binding mode is exemplified with the extra-mitochondrial cytochrome c (Cc), a well-known ANP32B partner and which now determine also binds to ANP32A; and with the RNA binding protein HuR, whose export to the cytoplasm is mediated by ANP32 proteins under stress. Therefore, differential expression patterns of ANP32A or ANP32B may affect the regulation of Cc and HuR and can help to explain the distinct roles of these proteins in diseases.
基因复制使得蛋白质能够朝着新的功能和机制进化。旁系同源基因之间的差异通常取决于无序区域的序列。例如,在哺乳动物中,伴侣蛋白ANP32A和ANP32B有着共同的进化路线,并且基于它们相似的N端结构域具有一些可互换的功能。然而,它们的C端低复杂性酸性区域(LCARs)显示出显著的序列差异,这揭示了它们之间一定程度的变异性,这与它们不同的组织特异性表达模式相一致。这些结构和计算结果表明,在核定位信号(NLS)附近,ANP32A中的脯氨酸被ANP32B中的苏氨酸取代,决定了C端LCAR的整体紧凑性。无序区域的不同结构特性影响了ANP32成员与其靶标的结合模式。这种不同的结合模式在胞外线粒体细胞色素c(Cc)中得到了体现,Cc是一种著名的ANP32B伴侣蛋白,现在也被确定能与ANP32A结合;还有RNA结合蛋白HuR,在应激状态下,其向细胞质的输出是由ANP32蛋白介导的。因此,ANP32A或ANP3B的差异表达模式可能会影响Cc和HuR的调控,并有助于解释这些蛋白质在疾病中的不同作用。