F-CphI represents a new homing endonuclease family using the Endo VII catalytic motif

• Published in: Mobile DNA 2018-08, Vol.9 (1), p.27-11, Article 27
• Main Authors: Fang, Xiaoting, Jiang, YongLiang, Li, Kim, Zeng, Qinglu
• Format: Article
• Language: English
• Subjects: Bacteriophage; Bioinformatics; Crystal structure; Deoxyribonucleic acid; DNA; Endonuclease VII; F-CphI; Genes; Genomes; Group I intron; Homing endonuclease; Logos; Mutagenesis; Phylogenetics; Proteins
• ISSN: 1759-8753; 1759-8753
• DOI: 10.1186/s13100-018-0132-5

There are six known families of homing endonucleases, LAGLIDADG, GIY-YIG, HNH, His-Cys box, PD-(D/E)-XK, and EDxHD, which are characterized by their conserved residues. Previously, we discovered a novel homing endonuclease F-CphI encoded by ORF177 of cyanophage S-PM2. F-CphI does not resemble any characterized homing endonucleases. Instead, the C-terminus of F-CphI aligns well with the N-terminal catalytic domain of a Holliday junction DNA resolvase, phage T4 endonuclease VII (Endo VII). A PSI-BLAST search resulted in a total of 313 Endo VII motif-containing sequences in sequenced genomes. Multiple sequence alignment showed that the catalytically important residues of T4 Endo VII were all well conserved in these proteins. Our site-directed mutagenesis studies further confirmed that the catalytically important residues of T4 Endo VII were also essential for F-CphI activity, and thus F-CphI might use a similar protein fold as Endo VII for DNA cleavage. A phylogenetic tree of the Endo VII motif-containing sequences showed that putative resolvases grouped into one clade while putative homing endonucleases and restriction endonucleases grouped into another clade. Based on the unique conserved residues, we proposed that F-CphI represents a new homing endonuclease family, which was named the DHHRN family. Our phylogenetic analysis could be used to predict the functions of many previously unknown proteins.