IS Families/IS481 family
Initially, IS481 appeared to be an IS3 family derivative which had been truncated for the N-terminal end of the Tpase and includes a C-terminal extension. The DDE active site domain and the IR (ending in 5’ TGT 3’) are similar to those of IS3 family members. Their presence in high copy number in some species and the identification of at least 130 distinct but related IS from over 90 species strongly suggests that these represent a distinct transpositionally active family. Different members generate DR of between 4 and 15 bp. Moreover, certain members (e.g. ISSav7) insert specifically into the tetranucleotide CTAG which becomes the flanking DR and provides the UAG termination codon for the Tpase. In contrast to the vast majority of IS3 family members, the IS481 Tpase is not produced by frameshifting. There is no evidence for a leucine zipper as in IS3.
Some members include passenger genes including antibiotic resistance (CmR for IS5564 and ISCgl1), or potential transcriptional regulators (ISKrh1, ISPfr21, ISSav7). IS481 itself has played a fundamental role in the evolution of the genomes of the Bordetellae where, in B. pertusis it has undergone extensive amplification to several hundred copies with accompanying genome decay.
These IS are distantly related to the eukaryotic Banshee transposon which at present is restricted to the anaerobic flagellated protozoan Trichomonas vaginalis (Pritham per. comm.). They share the highly conserved Pfam integrase core domain identified initially in the IS3 family and retroviruses. They also show a conserved 5’TG 3’ tip to the IR which is typical of this and other types of mobile elements. It would be interesting to determine whether Banshee transposes using a dsDNA circular intermediate as do IS3 family members.
IS1202 group (ISNCY)
A small group including IS1202, which had been included in the ISNCY (Not Classified Yet) group appears distantly related to IS481. Members are between 1400 and 1700 bp (except for ISKpn21 which includes a passenger gene annotated as "hypothetical protein”) with a Tpase orf of between 400 and 500 aa in a single reading frame. Their IR begin with TGT as do those of the IS3 and IS481 families. They generate DR of between 5 and, unusually, 27 bp.
They appear to have similarities at the level of their Tpases particularly in their DDE domains (e.g. IS1202 is 39% aa similar to ISPfr5 of the IS481 family). They include glutamine (Q) seven residues C-terminal to the conserved E instead of the characteristic K/R. Identification of additional IS will be necessary to clearly define this group.