Berna Anne, Bernier François, Chabrière Eric, Elias Mikael, Scott Ken, Suh Andrew
Institut de Biologie Moléculaire des Plantes du CNRS, Institut de Botanique, Université de Strasbourg, 28 rue Goethe, Strasbourg Cedex, France.
Cell Mol Life Sci. 2009 Jul;66(14):2205-18. doi: 10.1007/s00018-009-0006-6. Epub 2009 Mar 17.
DING proteins, identified mainly by their eponymous N-terminal sequences, are ubiquitous in living organisms. Amongst bacteria, they are common in pseudomonads, and have been characterised with respect to genetics and structure. They form part of a wider family of phosphate-binding proteins, with emerging roles in phosphate acquisition and pathogenicity. Many DING proteins have been isolated in eukaryotes, in which they have been associated with very diverse biological activities, often in the context of possible signalling roles. Disease states in which DING proteins have been implicated include rheumatoid arthritis, lithiasis, atherosclerosis, some tumours and tumour-associated cachexia, and bacterial and viral adherence. Complete genetic and structural characterisation of eukaryotic DING genes and proteins is still lacking, though the phosphate-binding site seems to be conserved. Whether as bacterial proteins related to bacterial pathogenicity, or as eukaryotic components of biochemical signalling systems, DING proteins require further study.
DING蛋白主要通过其同名的N端序列得以识别,在生物体内广泛存在。在细菌中,它们在假单胞菌中很常见,并且在遗传学和结构方面已有特征描述。它们是更广泛的磷酸盐结合蛋白家族的一部分,在磷酸盐获取和致病性方面发挥着新出现的作用。许多DING蛋白已在真核生物中分离出来,在真核生物中它们与非常多样的生物活性相关,通常在可能的信号传导作用的背景下。与DING蛋白有关的疾病状态包括类风湿性关节炎、结石病、动脉粥样硬化、一些肿瘤和肿瘤相关性恶病质,以及细菌和病毒黏附。尽管磷酸盐结合位点似乎是保守的,但真核生物DING基因和蛋白的完整遗传和结构特征仍不清楚。无论是作为与细菌致病性相关的细菌蛋白,还是作为生化信号系统的真核生物成分,DING蛋白都需要进一步研究。