PARALLEL EVOLUTION AND COEXPRESSION OF THE PROTEOLIPID PROTEINS AND PROTEIN ZERO IN VERTEBRATE MYELIN

Vertebrate myelin contains two proteins that mediate compaction: prote in zero (P-0), an immunoglobulin gene superfamily member, or proteolip id proteins, 4-hydrophobic domain-motif proteins biogenetically unrela ted to P-0. The prevailing view has been that expression of P-0 and pr oteolipid proteins is mutually exclusive; P-0, which mediates myelin c ompaction in fish, is thought to be completely replaced by the newer p roteolipid proteins in the terrestrial vertebrate CNS. However, we now find that proteolipid proteins are actually major myelin constituents in bony fish and amphibia, and so are coexpressed with P-0. Clearly, myelin proteolipids are not new additions to the myelin protein repert oire, but instead were ancestral sheath components, expressed similar to 440 million years ago in the first myelinated fish that existed at least similar to 100 million years before the origin of amphibians. In conclusion, P-0 and the proteolipid proteins are evolving in parallel in myelinating cells of most vertebrate species.