Conservation and Recombinational Contexts in Apoptosis Pathway in Aspergillus fumigatus

Dap Ns, C. D. Santos-Júnior, Macdo Pv, J. DaSilva, Alves Tc, Frstenau Cr, M. Desouza, Morais Er
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Abstract

Introduction: Aspergillus fumigatus is a highly pathogenic fungus for immunocompromised patients and invasive aspergillosis exhibits mortality rates around 50-80%. Thus, the apoptosis pathway in this fungus may be an important target for the development of new drugs. Materials and Methods: From a data bank, we analyzed five different proteins (Bax, Bir, Nma111, Pca1, and Rad9) belonging to the apoptosis pathway in the genome of Aspergillus fumigatus. Phylogenetic trees, splits graphs, recombination analyses, and assessment of selection strength from codon to codon were developed to understand the evolution and the function of these proteins in the fungus. Results: Our results suggest a conservation of these proteins in the Aspergillaceae family, as well as a low rate of gene recombination with a putative preservation of the function. Conclusion: We thus propose that the apoptosis pathway in Aspergillus fumigatus is started with the Rad9 protein followed by the activation of Bax and Pca1 proteins. Also, Nma111 cleaves the Bir protein resulting in the consequent activation of the Bax protein. Further studies are necessary to better understand the apoptosis process in Aspergillus fumigatus and to confirm the proteins belonging to the pathway.
烟曲霉凋亡通路的保护与重组背景
烟曲霉是免疫功能低下患者的高致病性真菌,侵袭性曲霉病的死亡率约为50-80%。因此,这种真菌的凋亡途径可能是开发新药的重要靶点。材料和方法:我们从数据库中分析了烟曲霉基因组中属于凋亡途径的5种不同蛋白(Bax、Bir、Nma111、Pca1和Rad9)。通过系统发育树、分裂图、重组分析和密码子间选择强度的评估来了解这些蛋白质在真菌中的进化和功能。结果:我们的研究结果表明,这些蛋白质在曲霉科中保存,并且基因重组率低,推测功能保存。结论:烟曲霉的凋亡途径是从Rad9蛋白开始的,然后是Bax和Pca1蛋白的激活。此外,Nma111切割Bir蛋白,从而导致Bax蛋白的激活。为了更好地了解烟曲霉的凋亡过程并确认属于该途径的蛋白,还需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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