Deis Rachael, Lerer-Goldshtein Tali, Baiko Olha, Eyal Zohar, Brenman-Begin Dolev, Goldsmith Moshe, Kaufmann Sylvia, Heinig Uwe, Dong Yonghui, Lushchekina Sofya, Varsano Neta, Olender Tsviya, Kupervaser Meital, Porat Ziv, Levin-Zaidman Smadar, Pinkas Iddo, Mateus Rita, Gur Dvir
Department of Molecular Genetics, Weizmann Institute of Science, Rehovot, Israel.
Department of Biomolecular Sciences, Weizmann Institute of Science, Rehovot, Israel.
Nat Chem Biol. 2025 Mar;21(3):383-392. doi: 10.1038/s41589-024-01722-1. Epub 2024 Aug 30.
Organisms evolve mechanisms that regulate the properties of biogenic crystals to support a wide range of functions, from vision and camouflage to communication and thermal regulation. Yet, the mechanism underlying the formation of diverse intracellular crystals remains enigmatic. Here we unravel the biochemical control over crystal morphogenesis in zebrafish iridophores. We show that the chemical composition of the crystals determines their shape, particularly through the ratio between the nucleobases guanine and hypoxanthine. We reveal that these variations in composition are genetically controlled through tissue-specific expression of specialized paralogs, which exhibit remarkable substrate selectivity. This orchestrated combination grants the organism with the capacity to generate a broad spectrum of crystal morphologies. Overall, our findings suggest a mechanism for the morphological and functional diversity of biogenic crystals and may, thus, inspire the development of genetically designed biomaterials and medical therapeutics.
生物体进化出调节生物源晶体特性的机制,以支持从视觉、伪装到通讯和体温调节等广泛的功能。然而,不同细胞内晶体形成的潜在机制仍然是个谜。在此,我们揭示了斑马鱼虹膜细胞中晶体形态发生的生化控制机制。我们表明,晶体的化学成分决定其形状,特别是通过核碱基鸟嘌呤和次黄嘌呤之间的比例。我们发现,这些成分变化是通过特定组织表达的专门旁系同源物进行基因控制的,这些旁系同源物表现出显著的底物选择性。这种精心编排的组合赋予生物体产生广泛晶体形态的能力。总体而言,我们的研究结果提出了一种生物源晶体形态和功能多样性的机制,因此可能会激发基因设计生物材料和医学治疗方法的发展。