Genome-Wide Reprogramming in the Mouse Germ Line Entails the Base Excision Repair Pathway

Author:

Hajkova Petra12,Jeffries Sean J.13,Lee Caroline1,Miller Nigel4,Jackson Stephen P.15,Surani M. Azim1

Affiliation:

1. Wellcome Trust–Cancer Research U.K. Gurdon Institute of Cancer and Developmental Biology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK.

2. Medical Research Council Clinical Sciences Centre, Hammersmith Hospital Campus, Du Cane Road, London W12 0NN, UK.

3. Templeman Automation, 21 Properzi Way, Somerville, MA 02143, USA.

4. Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK.

5. Department of Biochemistry, University of Cambridge, Cambridge CB2 1QW, UK.

Abstract

Erasing Markers Epigenetic reprogramming of the mammalian genome, which involves the removal and replacement of the various regulatory epigenetic marks such as DNA methylation, occurs during germ cell differentiation and during early zygotic development. This process is also critical during the experimental generation of stem cells, but the factors and pathways that control epigenetic reprogramming are not well understood. Hajkova et al. (p. 78 ) investigated the erasure of DNA methylation during germ cell differentiation and during early zygotic development in the developing mouse and found that factors involved in the base excision repair (BER) pathway, which helps repair damaged DNA, were involved. Furthermore, inhibitors of BER resulted in the retention of DNA methylation in the zygote.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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