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Phylogenetic analysis of eukaryotic NEET proteins uncovers a link between a key gene duplication event and the evolution of vertebrates

机译:真核N​​EET蛋白的系统发育分析揭示了关键基因复制事件与脊椎动物进化之间的联系。

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摘要

NEET proteins belong to a unique family of iron-sulfur proteins in which the 2Fe-2S cluster is coordinated by a CDGSH domain that is followed by the “NEET” motif. They are involved in the regulation of iron and reactive oxygen metabolism, and have been associated with the progression of diabetes, cancer, aging and neurodegenerative diseases. Despite their important biological functions, the evolution and diversification of eukaryotic NEET proteins are largely unknown. Here we used the three members of the human NEET protein family (CISD1, mitoNEET; CISD2, NAF-1 or Miner 1; and CISD3, Miner2) as our guides to conduct a phylogenetic analysis of eukaryotic NEET proteins and their evolution. Our findings identified the slime mold Dictyostelium discoideum’s CISD proteins as the closest to the ancient archetype of eukaryotic NEET proteins. We further identified CISD3 homologs in fungi that were previously reported not to contain any NEET proteins, and revealed that plants lack homolog(s) of CISD3. Furthermore, our study suggests that the mammalian NEET proteins, mitoNEET (CISD1) and NAF-1 (CISD2), emerged via gene duplication around the origin of vertebrates. Our findings provide new insights into the classification and expansion of the NEET protein family, as well as offer clues to the diverged functions of the human mitoNEET and NAF-1 proteins.
机译:NEET蛋白属于铁硫蛋白的独特家族,其中2Fe-2S簇由CDGSH结构域协调,随后是“ NEET”基序。它们参与铁和活性氧代谢的调节,并与糖尿病,癌症,衰老和神经退行性疾病的进展有关。尽管它们具有重要的生物学功能,但真核NEET蛋白的进化和多样化仍是未知之数。在这里,我们使用人类NEET蛋白家族的三个成员(CISD1,mitoNEET; CISD2,NAF-1或Miner 1;以及CISD3,Miner2)作为我们进行真核NEET蛋白及其进化系统分析的指南。我们的发现确定了粘液霉菌盘基网柄菌的CISD蛋白是最接近真核NEET古代原型的蛋白。我们进一步鉴定了以前报道不包含任何NEET蛋白的真菌中的CISD3同源物,并揭示了植物缺乏CISD3的同源物。此外,我们的研究表明,哺乳动物NEET蛋白mitoNEET(CISD1)和NAF-1(CISD2)通过脊椎动物起源周围的基因复制而出现。我们的发现为NEET蛋白家族的分类和扩展提供了新的见解,并为人类mitoNEET和NAF-1蛋白的多样化功能提供了线索。

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