Kelley Danielle S, Lennon Christopher W, Belfort Marlene, Novikova Olga
Department of Biomedical Sciences, School of Public Health, University at Albany, State University of New York, Albany, New York, USA.
Department of Biological Sciences and RNA Institute, University at Albany, State University of New York, Albany, New York, USA.
mBio. 2016 Oct 4;7(5):e01537-16. doi: 10.1128/mBio.01537-16.
Inteins are self-splicing protein elements that are mobile at the DNA level and are sporadically distributed across microbial genomes. Inteins appear to be horizontally transferred, and it has been speculated that phages may play a role in intein distribution. Our attention turns to mycobacteriophages, which infect mycobacteria, where both phage and host harbor inteins. Using bioinformatics, mycobacteriophage genomes were mined for inteins. This study reveals that these mobile elements are present across multiple mycobacteriophage clusters and are pervasive in certain genes, like the large terminase subunit TerL and a RecB-like nuclease, with the majority of intein-containing genes being phage specific. Strikingly, despite this phage specificity, inteins localize to functional motifs shared with bacteria, such that intein-containing genes have similar roles, like hydrolase activity and nucleic acid binding, indicating a global commonality among intein-hosting proteins. Additionally, there are multiple insertion points within active centers, implying independent invasion events, with regulatory implications. Several phage inteins were shown to be splicing competent and to encode functional homing endonucleases, important for mobility. Further, bioinformatic analysis supports the potential for phages as facilitators of intein movement among mycobacteria and related genera. Analysis of catalytic intein residues finds the highly conserved penultimate histidine inconsistently maintained among mycobacteriophages. Biochemical characterization of a noncanonical phage intein shows that this residue influences precursor accumulation, suggesting that splicing has been tuned in phages to modulate generation of important proteins. Together, this work expands our understanding of phage-based intein dissemination and evolution and implies that phages provide a context for evolution of splicing-based regulation.
Inteins are mobile protein splicing elements found in critical genes across all domains of life. Mycobacterial inteins are of particular interest because of their occurrence in pathogenic species, such as Mycobacterium tuberculosis and Mycobacterium leprae, which harbor inteins in important proteins. We have discovered a similarity in activities of intein-containing proteins among mycobacteriophages and their intein-rich actinobacterial hosts, with implications for both posttranslational regulation by inteins and phages participating in horizontal intein transfer. Our demonstration of multiple insertion points within active centers of phage proteins implies independent invasion events, indicating the importance of intein maintenance at specific functional sites. The variable conservation of a catalytic splicing residue, leading to profoundly altered splicing rates, points to the regulatory potential of inteins and to mycobacteriophages playing a role in intein evolution. Collectively, these results suggest inteins as posttranslational regulators and mycobacteriophages as both vehicles for intein distribution and incubators for intein evolution.
内含肽是自我剪接的蛋白质元件,在DNA水平上具有移动性,且零星分布于微生物基因组中。内含肽似乎是通过水平转移传播的,据推测噬菌体可能在其分布过程中发挥作用。我们将注意力转向感染分枝杆菌的分枝杆菌噬菌体,在噬菌体和宿主中都发现了内含肽。通过生物信息学方法,在分枝杆菌噬菌体基因组中挖掘内含肽。本研究表明,这些移动元件存在于多个分枝杆菌噬菌体簇中,并且在某些基因中普遍存在,如大型末端酶亚基TerL和一种类RecB核酸酶,大多数含内含肽的基因是噬菌体特有的。引人注目的是,尽管具有这种噬菌体特异性,内含肽却定位于与细菌共有的功能基序上,使得含内含肽的基因具有相似的功能,如水解酶活性和核酸结合,这表明含内含肽的蛋白质之间存在全球共性。此外,活性中心内有多个插入点,这意味着存在独立的入侵事件,具有调控意义。几种噬菌体内含肽被证明具有剪接能力,并编码功能性归巢内切酶,这对其移动性很重要。此外,生物信息学分析支持噬菌体作为分枝杆菌及相关属中内含肽移动促进因子的可能性。对催化性内含肽残基的分析发现,分枝杆菌噬菌体中倒数第二个组氨酸的高度保守性并不一致。对一种非典型噬菌体内含肽的生化特性分析表明,该残基影响前体积累,这表明噬菌体中的剪接过程已被调整以调节重要蛋白质的生成。总之,这项工作扩展了我们对基于噬菌体的内含肽传播和进化的理解,并意味着噬菌体为基于剪接的调控进化提供了一个背景。
内含肽是在生命所有领域的关键基因中发现的可移动蛋白质剪接元件。分枝杆菌内含肽特别令人感兴趣,因为它们存在于致病性物种中,如结核分枝杆菌和麻风分枝杆菌,这些细菌在重要蛋白质中含有内含肽。我们发现分枝杆菌噬菌体及其富含内含肽的放线菌宿主中含内含肽蛋白质的活性存在相似性,这对内含肽的翻译后调控以及参与内含肽水平转移的噬菌体都有影响。我们证明噬菌体蛋白质活性中心内有多个插入点意味着存在独立的入侵事件,这表明在特定功能位点维持内含肽很重要。催化剪接残基的可变保守性导致剪接速率发生深刻变化,这表明内含肽具有调控潜力,且分枝杆菌噬菌体在内含肽进化中发挥作用。总体而言,这些结果表明内含肽是翻译后调控因子,而分枝杆菌噬菌体既是内含肽分布的载体,也是内含肽进化的孵化器。