UMR 6632/IFR48, Université de Provence Aix Marseille 1/CNRS, F-13000, Marseille, France.
PLoS One. 2010 Nov 11;5(11):e15506. doi: 10.1371/journal.pone.0015506.
The Nme gene family is involved in multiple physiological and pathological processes such as cellular differentiation, development, metastatic dissemination, and cilia functions. Despite the known importance of Nme genes and their use as clinical markers of tumor aggressiveness, the associated cellular mechanisms remain poorly understood. Over the last 20 years, several non-vertebrate model species have been used to investigate Nme functions. However, the evolutionary history of the family remains poorly understood outside the vertebrate lineage. The aim of the study was thus to elucidate the evolutionary history of the Nme gene family in Metazoans.
METHODOLOGY/PRINCIPAL FINDINGS: Using a total of 21 eukaryote species including 14 metazoans, the evolutionary history of Nme genes was reconstructed in the metazoan lineage. We demonstrated that the complexity of the Nme gene family, initially thought to be restricted to chordates, was also shared by the metazoan ancestor. We also provide evidence suggesting that the complexity of the family is mainly a eukaryotic innovation, with the exception of Nme8 that is likely to be a choanoflagellate/metazoan innovation. Highly conserved gene structure, genomic linkage, and protein domains were identified among metazoans, some features being also conserved in eukaryotes. When considering the entire Nme family, the starlet sea anemone is the studied metazoan species exhibiting the most conserved gene and protein sequence features with humans. In addition, we were able to show that most of the proteins known to interact with human NME proteins were also found in starlet sea anemone.
CONCLUSION/SIGNIFICANCE: Together, our observations further support the association of Nme genes with key cellular functions that have been conserved throughout metazoan evolution. Future investigations of evolutionarily conserved Nme gene functions using the starlet sea anemone could shed new light on a wide variety of key developmental and cellular processes.
Nme 基因家族参与多种生理和病理过程,如细胞分化、发育、转移扩散和纤毛功能。尽管 Nme 基因的重要性及其作为肿瘤侵袭性的临床标志物已被广泛认识,但相关的细胞机制仍知之甚少。在过去的 20 年中,已经使用了几种非脊椎动物模型物种来研究 Nme 基因的功能。然而,除了脊椎动物谱系之外,该家族的进化历史仍知之甚少。因此,本研究旨在阐明 Nme 基因家族在后生动物中的进化历史。
方法/主要发现:使用总共包括 14 种后生动物的 21 种真核生物物种,重建了 Nme 基因在后生动物谱系中的进化历史。我们证明,Nme 基因家族的复杂性最初被认为仅限于脊索动物,也是后生动物祖先所共有的。我们还提供了证据表明,该家族的复杂性主要是真核生物的创新,除了 Nme8 可能是领鞭毛虫/后生动物的创新。后生动物中鉴定出高度保守的基因结构、基因组连锁和蛋白质结构域,其中一些特征在真核生物中也保守。当考虑整个 Nme 家族时,研究的后生动物物种星状海葵与人具有最保守的基因和蛋白质序列特征。此外,我们还能够表明,与人类 NME 蛋白相互作用的大多数已知蛋白也存在于星状海葵中。
结论/意义:总之,我们的观察结果进一步支持了 Nme 基因与关键细胞功能的关联,这些功能在后生动物进化过程中得到了保守。使用星状海葵对进化上保守的 Nme 基因功能的未来研究可能会为广泛的关键发育和细胞过程提供新的见解。