
κ-Casein-deficient mice fail to lactate
Author(s) -
P Chandra Shekar,
Sandeep Goel,
Sweta Rani,
D. Partha Sarathi,
Jomini Liza Alex,
Shashi Singh,
Satish Kumar
Publication year - 2006
Publication title -
proceedings of the national academy of sciences of the united states of america
Language(s) - English
Resource type - Journals
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0601611103
Subject(s) - casein , lactation , biology , mammary gland , allele , milk production , gene , genetics , biochemistry , zoology , pregnancy , cancer , breast cancer
Acquisition of milk production capabilities by an ancestor of mammals is at the root of mammalian evolution. Milk casein micelles are a primary source of amino acids and calcium phosphate to neonates. To understand the role of κ-casein in lactation, we have created and characterized a null mouse strain (Csnk −/− ) lacking this gene. The mutant κ-casein allele did not affect the expression of other milk proteins inCsnk −/− females. However, these females did not suckle their pups and failed to lactate because of destabilization of the micelles in the lumina of the mammary gland. Thus, κ-casein is essential for lactation and, consequently, for the successful completion of the process of reproduction in mammals. In view of the extreme structural conservation of the casein locus, as well as the phenotype ofCsnk −/− females, we propose that the organization of a functional κ-casein gene would have been one of the critical events in the evolution of mammals. Further, κ-casein variants are known to affect the industrial properties of milk in dairy animals. Given the expenses and the time scale of such experiments in livestock species, it is desirable to model the intended genetic modifications in mice first. The mouse strain that we have created would be a useful model to study the effect of κ-casein variants on the properties of milk and/or milk products.