Undermethylation of structural gene sequences in extraembryonic lineages of the mouse
The first two lineages to differentiate in the mouse embryo are the trophectoderm and primitive endoderm, which give rise to various extraembryonic structures only. Previous work has shown that all derivatives of these two lineages share the property of undermethylation of repetitive DNA sequences,...
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Published in: | Developmental biology Vol. 117; no. 2; pp. 567 - 573 |
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Language: | English |
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Elsevier Inc
01-10-1986
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Abstract | The first two lineages to differentiate in the mouse embryo are the trophectoderm and primitive endoderm, which give rise to various extraembryonic structures only. Previous work has shown that all derivatives of these two lineages share the property of undermethylation of repetitive DNA sequences, both satellite and dispersed. Here we show that this undermethylation is not a peculiarity of these repetitive elements but is also a feature of structural gene sequences within both lineages. α-Fetoprotein, albumin, and major urinary protein gene sequences all showed extensive undermethylation at
MspI restriction sites in extraembryonic lineages, which did not correlate with their expression in these tissues. The same sequences were heavily methylated in embryonic tissues as early as 7.5 days of development. There are, therefore, major global differences in DNA methylation between the earliest cell lineages to be established in the mouse embryo. The significance of these differences for cellular commitment events remains to be elucidated. |
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AbstractList | The first two lineages to differentiate in the mouse embryo are the trophectoderm and primitive endoderm, which give rise to various extraembryonic structures only. Previous work has shown that all derivatives of these two lineages share the property of undermethylation of repetitive DNA sequences, both satellite and dispersed. Here we show that this undermethylation is not a peculiarity of these repetitive elements but is also a feature of structural gene sequences within both lineages. alpha-Fetoprotein, albumin, and major urinary protein gene sequences all showed extensive undermethylation at MspI restriction sites in extraembryonic lineages, which did not correlate with their expression in these tissues. The same sequences were heavily methylated in embryonic tissues as early as 7.5 days of development. There are, therefore, major global differences in DNA methylation between the earliest cell lineages to be established in the mouse embryo. The significance of these differences for cellular commitment events remains to be elucidated. The first two lineages to differentiate in the mouse embryo are the trophectoderm and primitive endoderm, which give rise to various extraembryonic structures only. Previous work has shown that all derivatives of these two lineages share the property of undermethylation of repetitive DNA sequences, both satellite and dispersed. Here we show that this undermethylation is not a peculiarity of these repetitive elements but is also a feature of structural gene sequences within both lineages. α-Fetoprotein, albumin, and major urinary protein gene sequences all showed extensive undermethylation at MspI restriction sites in extraembryonic lineages, which did not correlate with their expression in these tissues. The same sequences were heavily methylated in embryonic tissues as early as 7.5 days of development. There are, therefore, major global differences in DNA methylation between the earliest cell lineages to be established in the mouse embryo. The significance of these differences for cellular commitment events remains to be elucidated. |
Author | Andrews, G.K. Chapman, V.M. Rossant, J. Sanford, J.P. |
Author_xml | – sequence: 1 givenname: J. surname: Rossant fullname: Rossant, J. organization: Department of Biological Sciences, Brock University, St. Catharines, Ontario, Canada L2S 3A1 – sequence: 2 givenname: J.P. surname: Sanford fullname: Sanford, J.P. organization: Department of Molecular Biology, Roswell Park Memorial Institute, Buffalo, New York 14263 USA – sequence: 3 givenname: V.M. surname: Chapman fullname: Chapman, V.M. organization: Department of Molecular Biology, Roswell Park Memorial Institute, Buffalo, New York 14263 USA – sequence: 4 givenname: G.K. surname: Andrews fullname: Andrews, G.K. organization: Department of Biochemistry, Kansas State University, Kansas City, Kansas 66103 USA |
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Keywords | Vertebrata Mammalia Mouse Repeated sequence DNA Rodentia Structure gene Methylation |
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SubjectTerms | Albumins - genetics alpha-Fetoproteins - genetics Animals Biological and medical sciences Cell differentiation, maturation, development, hematopoiesis Cell physiology Deoxyribonuclease HpaII DNA Restriction Enzymes Ectoderm - physiology Endoderm - physiology Ethidium Extraembryonic Membranes - physiology Fundamental and applied biological sciences. Psychology Gene Expression Regulation Genes Liver - embryology Methylation Mice Molecular and cellular biology Proteins - genetics Trophoblasts - physiology Yolk Sac - physiology |
Title | Undermethylation of structural gene sequences in extraembryonic lineages of the mouse |
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