The search strategy outlined above identified nume rous families

The search strategy outlined above identified nume rous families of domains as being new versions of the HEPN domain. Stri kingly, we observed that several of these newly recognized families correspond to the catalytic domains of RNases that have been previously biochemically characterized. These include the mRNA cleaving RNase LS family im plicated in the defense against enterobacteriophage T4, the tRNA anti codon loop cleaving RNase domains of RloC and PrrC also involved in the restriction of T4, and the kinase extension nuclease domain of RNase L which is involved in specialized splicing reactions and interferon induced antiviral res ponse in vertebrates. Consistent with these results, we also detected a novel version of HEPN domain in the pan eukaryotic Las1 proteins involved in the cleavage and processing of the ITS2 linker RNA which separates the 5. 8S and 25S 28S rRNAs in their common precursor.
The eukaryotic additional hints Swt1 proteins, which are involved in the degradation of pre mRNA at the nuclear pore to prevent their exit to the cytoplasm, also displayed a previously unknown version of HEPN domain. Many of the newly detected HEPN families showed additional connections to antiviral defense functions. Most notably, 6 families of domains, respectively typified by the AbiD, AbiF, AbiJ, AbiU2, AbiV and the C terminal domain of AbiA, which are products of the eponymous abortive phage infection genes from Lacto coccus lactis, were characterized as novel versions of the HEPN domain. We also identified novel ver sions of the HEPN domain that comprised the C terminal modules in a large group of COG1517 related proteins, which are encoded by genes found in a subset of the CRISPR Cas loci. These findings suggested previously unappreciated roles of HEPN domains in RNA processing, both in defense and in cellular RNA maturation.
Importantly, these observations raised the possibility that at least a subset of HEPN domains might function as RNases with diverse target specificities. Beyond the above noted families, custom peptide synthesis our analysis reco vered at least 38 distinct families of domains that belong to the HEPN superfamily several of which can be further grouped together into higher order assemblages based on preferential recovery in profile or profile profile searches. These include functionally enigmatic families such as the MtlR family of regulatory proteins typified by the Escherichia coli man nitol operon regulators. Other new HEPN domain families are labeled as domains of unknown function in the PFAM database, namely DUF3644, DUF4209, DUF2526, Ymh.

The search strategy outlined above identified nume rous families