Department of Molecular Microbiology, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, México.
Centro Andaluz de Biología del Desarrollo, Consejo Superior de Investigaciones Científicas/Universidad Pablo de Olavide/Junta de Andalucía, Seville, Spain.
J Bacteriol. 2020 Dec 18;203(2). doi: 10.1128/JB.00413-20.
In prokaryotes, the key players in transcription initiation are sigma factors and transcription factors that bind to DNA to modulate the process, while premature transcription termination at the 5' end of the genes is regulated by attenuation and, in particular, by attenuation associated with riboswitches. In this study, we describe the distribution of these regulators across phylogenetic groups of bacteria and archaea and find that their abundance not only depends on the genome size, as previously described, but also varies according to the phylogeny of the organism. Furthermore, we observed a tendency for organisms to compensate for the low frequencies of a particular type of regulatory element (i.e., transcription factors) with a high frequency of other types of regulatory elements (i.e., sigma factors). This study provides a comprehensive description of the more abundant COG, KEGG, and Rfam families of transcriptional regulators present in prokaryotic genomes. In this study, we analyzed the relationship between the relative frequencies of the primary regulatory elements in bacteria and archaea, namely, transcription factors, sigma factors, and riboswitches. In bacteria, we reveal a compensatory behavior for transcription factors and sigma factors, meaning that in phylogenetic groups in which the relative number of transcription factors was low, we found a tendency for the number of sigma factors to be high and vice versa. For most of the phylogenetic groups analyzed here, except for and , a clear relationship with other mechanisms was not detected for transcriptional riboswitches, suggesting that their low frequency in most genomes does not constitute a significant impact on the global variety of transcriptional regulatory elements in prokaryotic organisms.
在原核生物中,转录起始的关键因子是σ因子和转录因子,它们与 DNA 结合以调节转录过程,而基因 5'端的过早转录终止则由衰减调节,特别是由与核糖体开关相关的衰减调节。在这项研究中,我们描述了这些调节因子在细菌和古菌的系统发育群中的分布,并发现它们的丰度不仅取决于先前描述的基因组大小,还根据生物体的系统发育而变化。此外,我们观察到生物体有一种倾向,即用高频率的其他类型的调节因子(即σ因子)来补偿特定类型的调节元件(即转录因子)的低频率。这项研究提供了一个关于原核生物基因组中更丰富的 COG、KEGG 和 Rfam 转录调节因子家族的全面描述。在这项研究中,我们分析了细菌和古菌中主要调节元件(即转录因子、σ因子和核糖体开关)的相对频率之间的关系。在细菌中,我们揭示了转录因子和σ因子之间的补偿行为,这意味着在转录因子相对数量较低的系统发育群中,我们发现σ因子的数量有增加的趋势,反之亦然。对于大多数在这里分析的系统发育群,除了和 ,对于转录核糖体开关,没有检测到与其他机制的明显关系,这表明它们在大多数基因组中的低频率对原核生物中全球转录调节因子的多样性没有显著影响。