Lees Murdock, Diane, Shovlin, TC, Gardiner, T, De Felici, M and Walsh, CP (2005) DNA methyltransferase expression in the mouse germ line during periods of de novo methylation. DEVELOPMENTAL DYNAMICS, 232 (4). pp. 992-1002. [Journal article]
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DNA methyltransferase (DNMT) 3A and DNMT3B are both active de novo DNA methyltransferases required for development, whereas DNMT3L, which has no demonstrable methyltransferase activity, is required for methylation of imprinted genes in the oocyte. We show here that different mechanisms are used to restrict access by these proteins to their targets during germ cell development. Transcriptional control of the Dnmt3l promoter guarantees that message is low or absent except during periods of de novo, activity. Use of an alternative promoter at the Dnmt3a locus produces the shorter Dnmt3a2 transcript in the germ line and postimplantation embryo only, whereas alternative splicing of the Dnmt3b transcript ensures that Dnmt3b1 is absent in the male prospermatogonia. Control of subcellular protein localization is a common theme for DNMT3A and DNMT3B, as proteins were seen in the nucleus only when methylation was occurring. These mechanisms converge to ensure that the only time that functional products from each locus are present in the germ cell nuclei is around embryonic day 17.5 in males and after birth in the growing oocytes in females. (c) 2005 Wiley-Liss, Inc.
|Item Type:||Journal article|
|Faculties and Schools:||Faculty of Life and Health Sciences > School of Biomedical Sciences|
Faculty of Life and Health Sciences
|Research Institutes and Groups:||Biomedical Sciences Research Institute > Genomic Medicine > Transcriptional Regulation & Epigenetics|
Biomedical Sciences Research Institute > Genomic Medicine
Biomedical Sciences Research Institute
|Deposited By:||Professor Colum Walsh|
|Deposited On:||02 Apr 2012 09:57|
|Last Modified:||11 Dec 2012 14:33|
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