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Letters to Nature
Nature 294, 450 - 451 (03 December 1981); doi:10.1038/294450a0

Evidence for expression of the paternal genome in the two-cell mouse embryo

Janet A. Sawicki, Terry Magnuson & Charles J. Epstein

Departments of Pediatrics and of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, California 94143, USA

Although there is strong evidence that the paternal genome is activated at the four- to eight-cell stage of mouse embryogenesis1–12, studies to date have been restricted because of their dependence on the manifestations of gene products, such as enzyme activity and cell-surface expression, rather than on direct assay of their synthesis. beta 2-microglobulin (beta 2M), a 12,000-molecular weight (M r) peptide associated with several of the gene products encoded by the H–2–Tla complex in the mouse13–17, is synthesized by early cleavage stage embryos (J.A.S., T.M. and C.J.E., unpublished). The existence of an electrophoretic variant of beta 2M in inbred strains has recently been described18–20, and tryptic peptide mapping19 and amino acid sequencing data21 indicate that the primary sequences of these variants differ by a single amino acid, thus establishing the genetic basis for this variation. Mice heterozygous at the beta 2m locus synthesize both forms, beta 2Ma and beta 2Mb (refs 18, 20). Using direct immunoprecipitation and two-dimensional gel electrophoresis, we have used this variation at the beta 2m locus to distinguish between maternal and paternal beta 2M and have now established that the synthesis of paternally derived beta 2M is first detectable at the two-cell stage. This is the earliest stage at which expression of the mammalian embryonic genome has been established22.

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