Table 1.
Chick | Mouse | Xenopus | Zebrafish | |
---|---|---|---|---|
Development | Internal (oviduct for cleavage stage)/external | In utero | External | External |
Developmental specificity | Early development like mammals (primitive streak) | Mammalian | Metamorphosis | Early development phases quite different to other vertebrates. |
Developmental cycle length | 22 days | 18–21 days | 4 days (at 23°C), temperature dependent | 2–3 days |
Offspring | <10 | <10 | 103 | 102 |
Oocyte size (diameter) | 2.5 cm | 80–100 μm | 1.2–1.4 mm | 0.7 mm |
Maintenance and breeding | Easy but need to obtain laid eggs | Difficult and expensive | Very easy | Very easy |
Manipulative embryology | Access through the egg shell (graft, beads implantation) | Only for embryos up to blastocyst stage but need to be re-implanted | Microsurgery, graft, fate mapping | Microsurgery, fate mapping |
Genome | Sequenced (1.2 × 109) | Sequenced (3 × 109) | Tetraploid genome not yet sequenced but X tropicalis genome (1.8 × 109) sequenced | Sequenced (1.7 × 109) duplicated genome |
Genetics based techniques | Spontaneous mutations, gene silencing (RNAi), electroporation, transgenic animal (lentivirus), ES cells | Electroporation, KO, KI, conditional transgenesis | Gene silencing (MO), gain of functions (injection RNA, protein, DNA), transgenic animal (REMI) | KO, gene silencing and gain of functions as Xenopus embryos but no targeted injections |
Screens | Mutation screens (but costly and difficult) | Mutation screens | Pharmacological and mutation screens | Pharmacological and mutation screens |
Specific advantages | Chimera | ES cells, iPS | Targeted injections, high resistance to infections | Transparency of embryos |
Website | MGI | Xenbase | ZFIN |
ES embryonic cells, iPS induced pluripotent cells, KO knock-out, KI knock-in, MO morpholino oligonucleotide, REMI restriction enzyme-mediated insertion