Genomic imprinting is an epigenetic mode of gene regulation that results in expression of the autosomal ‘imprinted’ genes from only a single allele, determined exclusively by parental origin. To date over 20 imprinted genes have been identified in mouse and man and these appear to lie in clusters in restricted regions on a subset of chromosomes. This may be a critical feature of imprinting suggesting a domain-type mode of regulation. Imprinted domains are replicated asynchronously, show sex-specific meiotic recombination frequencies and have CpG-rich regions that are differentially methylated, often associated with the imprinted genes themselves. Mouse distal chromosome 7 is one such domain, containing at least nine imprinted genes spanning over 1 Mb of DNA. For the maternally expressed p57Kip2 gene, passage through the female germline is essential to generate the active state, whereas passage through the male germline is needed to force the maternally expressed H19 gene into an inactive state. It is therefore possible that the mouse distal chromosome 7 imprinted domain is actually composed of two or more independently regulated subdomains.

In non-ruminant livestock the energy which can be derived from dietary cellulose and xylan is limited by the inefficient microbial fermentation of these polymers in the hind-gut. Furthermore, in poultry, cereal-derived plant structural polysaccharides impair normal digestive function through the formation of gel-like structures that trap nutrients which are therefore unavailable to the animal. The nutrition of non-ruminant livestock could be significantly improved by the depolymerization of plant structural polysaccharides, through the introduction of cellulase activity in the small intestines of these animals. This report describes the generation of transgenic animals with the capacity to express and secrete a functional endoglucanase from the exocrine pancreas.

The gene encoding endoglucanase E (celE) from Clostridium thermocellum was fused to the exocrine pancreas specific enhancer of the elastase I gene and the (β-globin polyadenylation signal, and used to create 14 lines of transgenic mice. A range of tissues were assayed for cellulase activity, using β-glucan and 4-methylumbelliferyl-β-D-cellobioside as substrates. The pancreas was also subjected to immunohistochemistry and in situ hybridization.