In humans, at least 44 members are known. Our results indicate that inbreeding and small effective population size (Ne) of zebrafish lab strains has led to the predicted effects of reduced variation within and divergence among strains. 10.1074/jbc.275.6.3781. The larger genome size of zebrafish compared to fugu and medaka (V enkatesh et al. We examined genetic variation at 1832 polymorphic EST‐based single nucleotide polymorphisms (SNPs) and the cytb mitochondrial gene in 13 wild populations and three lab strains. Our phylogenic trees also demonstrate groups such as CCL17/20, CCL19/21/25, CCL27/28 and fishspecific groups (Figure 2A). 4a). 2004; Gray et al. mtDNA sequence divergence allows approximate calculations of divergence times among several of the genetic groups. Another leading candidate gene for the influence of domestication was tpm3, although it was associated with a synonymous substitution. 10.1093/molbev/msl150. Therefore, characterization of other chemokine functions in embryos may elucidate the molecular basis of the dynamic movements of various types of cells during vertebrate development. The achieved scaffold N50 is 7.6 Mb, reaching a relatively high level among sequenced fish species. CAS  ... in contrast, the mid-sized zebrafish genome is ~ 1.5 Gb in size, but contains over 58% of repetitive elements. (2002) (N = 66), (3) high‐quality predicted SNPs from Guryev et al. (2006). 2003). Blood. Compared to the other chemokines that are approximately 100 amino acids (a.a.) long, these three chemokines are much longer (Table 1), and the transmembrane segments are located at positions 133–155 of CXCL-chr24a (187 a.a. long), 132–153 of CXCLchr24b (153 a.a. long), and 133-155 of CXCL-chr24d (210 a.a. long). All SNP ... We used nonoverlapping 10 Mb sliding windows from throughout the genome to calculate the genome‐wide distribution from nonoutlier windows. Li Q, Shirabe K, Kuwada JY: Chemokine signaling regulates sensory cell migration in zebrafish. On the other hand, the pufferfishes have few such chemokines like mammals (see Additional file 1). Research on lab strains that incorporates genetic variation from wild populations will enhance understanding of modifiers of a rich array of existing mutants and genotype‐phenotype associations discovered in lab strains. All assays were done in triplicate and the results were expressed as the mean number of cells per 0.4 mm3. In contrast, each of the lab strains (AB, SJA and TM1) was monomorphic (Table 2). Copy number variants are likewise ∼1.5-fold more prevalent in zebrafish than in human genomes (Brown et al., 2012). Although Gilligan et al. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Based on the arrangement of the four conserved cysteine residues, chemokines are now classified into four subfamilies, CXC, CC, XC and CX3C. The percentile at which each outlier locus occurred was used as a P‐value for deviation from the genome‐wide average and a significance cutoff of P < 0.05 was used. When the genome organization is compared with the phylogenetic tree (Figure 2), zebrafish genes consisting of the same major or mini-clusters also tend to locate in the same branches of the phylogenetic tree. The zebrafish chemokine genes are distributed on 17 different chromosomes, but 10 genes have not yet been localized on any chromosomes. BMC Genomics Nature reviews. Nonrandom aggregations of significant FST outliers along chromosomes would be consistent with ‘hotspots’ or genomic regions with multiple loci that have been influenced by selection. DeVries ME, Kelvin AA, Xu L, Ran L, Robinson J, Kelvin DJ: Defining the origins and evolution of the chemokine/chemokine receptor system. DeVries et al. Fig. Nat Immunol. The three lab strains we examined were derived from U.S. pet stores, and the mtDNA results suggest that they originally were collected from the Ganges/Brahmaputra region, likely near the major city Kolkata (Calcutta). Zebrafish: Housing and husbandry recommendations. Based on the analyses on the genome organization, phylogenetic trees, and synteny, zebrafish chemokines can be divided into zebrafish-specific genes including CX subfamily members, fish-specifi genes, several genes moderately similar to human chemokines, and genes orthologous to human homeostatic chemokines CXCL12 and CXCL14. 2001, 78: 57-110. [http://www.cbs.dtu.dk/services/NetOGlyc/], SOSUI. Sixteen of the 75 (21%) high outliers and four of the 22 (18%) low outliers were also identified when lab strains were excluded from the analysis. Moss, Stephen P., Joyce, Domino A., Humphries, Stuart et al, Tindall, Katherine J. and Lunt, David H. (2011) Comparative analysis of teleost genome sequences reveals an ancient intron size expansion in the zebrafish lineage. GRCz11 shows a significant reduction in scaffold numbers and increase in scaffold N50 whilst the overall genome size was not affected. Molecular Biology and Evolution. The southern Bangladesh population (CHT) was also genetically differentiated (Table S2, Supporting information). By multiplying the estimated size of the zebrafish genome (1.45 × 10 3 Mb) by the mutation rate detected by TILLING (2–4 mutations per megabase), an estimate of the number of ENU-induced mutations per F1 fish is ∼3–6000. The largest zebrafish LG chromosomes (5 and 7) were slightly larger than human chromosome 18 (76.12 Mb) and the smallest zebrafish LG chromosomes (22 and 25) were similar to the size of human chromosome 21 (46.94 Mb). 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