ition, medaka chromosome 17 contains the following gnathostome ancestor chromosome elements: 1a, 1c, 19a, and 19c. The area on Hsa 10 where we found synteny with both the AgRP2 and ASIP2, contains the gnathostome ancestor chromosome 10 elements, and the area on Hsa 19 that we found to have synteny with Ola 17 contains 19a, 19b, and 19c. The region on medaka chromosome 3, containing AgRP1, derives from a completely different region, the gnathostome ancestor chromosome element 15. Among the previously identified putative synteny regions and the ones that we have identified here that contain ARN-509 web Agouti-like areas in the human genome, it is only Hsa 8 and Hsa 16 that are convincingly derived from ancestral vertebrate proto-chromosome B which is found in the amniote and osteichthyan ancestor. The other areas are more likely related to J, E and D, and A. The regions containing the A2 genes in medaka are not only related to proto-chromosome B, but also to A, E, and F. In Discussion The lack of sequences has hampered studies of the evolution of the Agouti-like peptides. 
We therefore expanded the sequence pool of vertebrate Agouti-like sequences, which in turn enabled us to develop a sensitive, profile-hidden Markov model for long-range searches. Using these models and PHI-BLAST searches, we surprisingly found eight novel homologues from the phylum arthropods and three from the phylum ascomycota in the fungi kingdom that have similarities with PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/22202440 Agouti-like peptides. Importantly, the sequences in arthropods have the characteristic C-xC-C motif which are present in the Agouti-like sequences. The three sequences from fungi have however the longer C-x-C-C motif instead of the C-x-C-C motif but these three sequences have also the C–P motif and the C-A motif that are conserved in most of the AgRP and ASIP-like sequences. These sequences do not only share these characteristic motifs but they also have the approximate sequence length, and positioning of the motif sequence, i.e. in the end, that matches the vertebrate Agouti-like sequences. Moreover, we found that two of the sequences, one from the African malaria mosquito and another one from the Southern house mosquito share exon-intron structures that are similar to the other Agouti-like peptides, providing further support for the common origin of these sequences. The sequence that is the most similar to any vertebrate Agouti-like sequence is a venom peptide from Mojave Desert spider that contains a cysteine knot identical to AgRP2. It is unlikely that these Agouti-like sequences in arthropods or in fungi are functioning through MC receptors as the most ancient evidence of the MC receptors is found in sea lamprey. Moreover, inhibitor cystein knot structures in spider venom peptides are thought to give the proteins stability and protection against proteases, and in spiders, ICK proteins are known to block ion channels, not GPCRs. We made a large effort to annotate a number of vertebrate Agouti-like sequences. We have added more than twice as many new A2 sequences from different sources such as from mining of new genomes, experimental sequencing, and by using ESTs imported from Kurokawa et al. . The new sequences give us a more complete view of which sequence motifs, and which exon-intron structures, are typical of A2 sequences. The larger A2 sequence pool has allowed us to identify a new A2 motif, present in the second coding exon of all known A2 sequences, ��LF-A-R”. Furthermore, in the A2 cysteine knot –
