Louis-Marie Houdebine and Jianglin Fan The study of biological functions of proteins and their possible roles in the pathogenesis of human diseases requires more and more relevant animal m- els. Although mice including genetically modified mice offer many possibilities, other non-murine species are absolutely required in some circumstances. Rabbit is one of these species, which has been widely used in biomedical studies. This animal is genetically and physiologically closer to humans including cardiov- cular system and metabolism characteristics. Rabbit is thus more appropriate than mice to study some diseases such as atherosclerosis and lipid metabolism. Because of its larger size, surgery manipulation, bleeding, and turn-over studies are much easier performed in rabbits than in mice. Furthermore, transgenic rabbits can be produced using microinjection and other methods such as lentiviral v- tors. Cloning in rabbits has been proved possible, even though still laborious and time-consuming. Hopefully, functional rabbit ES cell lines will be available in the coming years. Gene deletion or knock-out in rabbits will then become possible.
It is clear that with the progress of genome sequencing, ES cells culture, cloning, transgenesis and interfering RNAs and other techniques, rabbit biotechnology is entering a new era. It is a good time to emphasize this fact by the publication of this book
1 Introduction, L.M. Houdebine, J. Fan; 2 Improvement of rabbit production, Kitajima S.; 3 Basic Methods for Experimental Rabbits, Nishijima K.; 4 Useful information for rabbit genes, proteins and antibodies, Koike T, Zhang J and Fan J.; 5 Rabbit transgenesis, Kitajima S, Liu E and Fan J.; 6 Rabbit as a model for the study of human diseases, Shiomi M.; 7 Transgenic rabbits to prepare pharmaceutical protein, Houdebine LM, Jolivet G and Ripoll P J.; 8 Derivation and characterization of rabbit embryonic stem cells: a review, Goza E and Bösze Z.; 9 Rabbit Cloning, Dinnyes A, Polgar Z and Meng Q.; 10 The European rabbit genome, Alföldi J, Di Palma F, and Lindblad-Toh K.