
The major ADP-ribosylating enzyme families are the focus of this special issue of Frontiers in Bioscience . However, there is room for another family of enzymes with the capacity to utilize nicotinamide adenine dinucleotide (NAD): the ADP-ribosyl cyclases (ARCs). These unique enzymes catalyse the cyclization of NAD to cyclic ADP ribose (cADPR), a widely distributed second messenger. However, the ARCs are versatile enzymes that can manipulate NAD, NAD phosphate (NADP) and other substrates to generate various bioactive molecules including nicotinic acid adenine dinucleotide diphosphate (NAADP) and ADP ribose (ADPR). This review will focus on the group of well-characterized invertebrate and vertebrate ARCs whose common gene structure allows us to trace their origin to the ancestor of bilaterian animals. Behind a facade of gene and protein homology lies a family with a disparate functional repertoire dictated by the animal model and the physical trait under investigation. Here we present a phylogenetic view of the ARCs to better understand the evolution of function in this family.
GPI-Linked Proteins, NAD, ADP-ribosyl Cyclase 1, Evolution, Molecular, Species Specificity, Antigens, CD, Animals, Humans, evolution; gene family; ADP-ribosyl cyclase, ADP-ribosyl Cyclase, Phylogeny
GPI-Linked Proteins, NAD, ADP-ribosyl Cyclase 1, Evolution, Molecular, Species Specificity, Antigens, CD, Animals, Humans, evolution; gene family; ADP-ribosyl cyclase, ADP-ribosyl Cyclase, Phylogeny
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