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Genetic imprinting in the mouse: Implications for gene regulation

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Journal of Inherited Metabolic Disease

Summary

Genetic imprinting specifies a germline marking that subsequently results in the repression of one or other parental allele at some point in development. Genetic manipulations to generate maternal and paternal duplications of specific chromosome regions have been used to screen almost the entire mouse genome for evidence of imprinting. As a result, 15 imprinting effects involving 10 regions on 6 different chromosomes have been detected that range from early embryonic lethalities to various growth and developmental defects seen only after birth. Genes with important roles in development therefore appear to be involved. Diverse studies have identified four imprinted genes, all of which show monoallelic expression in some, but not necessarily all, tissues. A correlation with methylation is indicated but the pattern of methylation is not consistent for each of the genes; methylation is therefore unlikely to be the imprinting signal. Methods being used to identify further imprinted genes are summarized and some of the difficulties posed are indicated.

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  1. MRC Radiobiology Unit, OX11 0RD, Chilton, Didcot, Oxon, UK

    B. M. Cattanach & J. Jones

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Cattanach, B.M., Jones, J. Genetic imprinting in the mouse: Implications for gene regulation. J Inherit Metab Dis 17, 403–420 (1994). https://doi.org/10.1007/BF00711356

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