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. 2018 Feb 14;9(2):96. doi: 10.3390/genes9020096

Table 1.

Main cytogenomic traits in fish-like chordates.

Group 2n Chromosome Counts (Basic Features) Micro- Chromosomes CG Heterogeneity WGD after the First Two Basal Vertebrates´ WGDs C-value/Haploid DNA Content (pg) [12] Specific Features in the Genome History and Chromosomal Evolution
Myxiniformes (hagfishes) 14–48 NO unknown not observed Myxinidae 2.5–4.59 chromatin diminution, programmed genome rearrengement [13,14]
Petromyzontiformes (lampreys) 76–178 NO GC-rich DNA repeats not observed Petromyzontidae 1.29–2.5 programmed genome rearrengement [14]
Chondrichthyes (cartilaginous fishes) 54–102 YES observed, presumably satellite DNA not observed Chimeriformes 1.5-2 Selachimorpha ~3–17 Rajimorphii 2.7–17 AT/GC heterogeneity positively correlated with genome size [15]
Ceratodontiformes (lungfishes) 34–68 Only N. forsteri [15] otherwise not unknown not observed Neoceradotus 52.75–74.86
Lepidosiren 80.55–123.9
Protopterus 40–132.8
“genomic obesity” without WGD documented [16,17]
Coelacanthiformes (lobe-finned fishes) 48 YES unknown not observed Latimeria 2.8–6.6 chromosomes similar to ancient frogs [18]
Acipenseriformes (sturgeons, paddlefish) ~ 120–240–360 YES ~ 50% NORs and GC-rich microchromosomes [7] andG-banding [19,20] multiple in sturgeons, one in paddlefish Acipenser 1.8–9.3
Polyodon 1.6–2.4
multiple WGD, ploidy diversity
Lepisosteiformes (gars) 56–58 small sized chromosomes in both genera not observed Atractosteus 1.2
Lepisosteus 1.4
regionally high recombination rate
Amiiformes (bowfin) 46 NO only NORs not observed Amia calva 1.2 convergent evolution with teleosts?
Polypteriformes (bichirs) 36–38 biarmed, extremelly large NO only NORs not observed Erpetoichthys 4.5
Polypterus 3.6-7.2
not investigated
Teleostei ~ 50 (exceptions up to 100–150 or more) Micro B-chromosomes only NORs TGD and lineage specific WGDs mostly 0.4- ~ 1.0 from genome compaction to lineage specific WGD

WGD: Whole-genome duplication; NOR: Nucleolar organizer region; pg: picograms.

a orders and families mostly based on [22]; b c-value, based on [12] database; c n: based on genomic/sequence data, originates from NCBI, 2n based on cytogenetic data [86]; d number of assemblies currently released and level of assembly (C = contig, D = draft, S = scaffold, Ch = chromosomal level); e Sequencing methods (I = Illumina, PB = PacBio, S = Sanger), linkage map (LM) available.