| Literature DB >> 19771477 |
Steven J Siegel1, Caroline M Percopo, Kimberly D Dyer, Wei Zhao, V Louise Roth, John M Mercer, Helene F Rosenberg.
Abstract
The RNase A ribonucleases are a complex group of functionally diverse secretory proteins with conserved enzymatic activity. We have identified novel RNase 1 genes from four species of squirrel (order Rodentia, family Sciuridae). Squirrel RNase 1 genes encode typical RNase A ribonucleases, each with eight cysteines, a conserved CKXXNTF signature motif, and a canonical His(12)-Lys(41)-His(119) catalytic triad. Two alleles encode Callosciurus prevostii RNase 1, which include a Ser(18)<-->Pro, analogous to the sequence polymorphisms found among the RNase 1 duplications in the genome of Rattus exulans. Interestingly, although the squirrel RNase 1 genes are closely related to one another (77-95% amino acid sequence identity), the cluster as a whole is distinct and divergent from the clusters including RNase 1 genes from other rodent species. We examined the specific sites at which Sciuridae RNase 1s diverge from Muridae/Cricetidae RNase 1s and determined that the divergent sites are located on the external surface, with complete sparing of the catalytic crevice. The full significance of these findings awaits a more complete understanding of biological role of mammalian RNase 1s.Entities:
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Year: 2009 PMID: 19771477 PMCID: PMC2809794 DOI: 10.1007/s00335-009-9215-4
Source DB: PubMed Journal: Mamm Genome ISSN: 0938-8990 Impact factor: 2.957