Genome-scale DNA methylation maps of pluripotent and differentiated cells

被引:0
|
作者
Alexander Meissner
Tarjei S. Mikkelsen
Hongcang Gu
Marius Wernig
Jacob Hanna
Andrey Sivachenko
Xiaolan Zhang
Bradley E. Bernstein
Chad Nusbaum
David B. Jaffe
Andreas Gnirke
Rudolf Jaenisch
Eric S. Lander
机构
[1] Whitehead Institute for Biomedical Research,Department of Stem Cell and Regenerative Biology
[2] 9 Cambridge Center,Division of Health Sciences and Technology
[3] Cambridge,Department of Pathology
[4] Massachusetts 02142,Department of Biology
[5] USA ,Department of Systems Biology
[6] Broad Institute of MIT and Harvard,undefined
[7] 7 Cambridge Center,undefined
[8] Cambridge,undefined
[9] Massachusetts 02142,undefined
[10] USA ,undefined
[11] Harvard University,undefined
[12] Cambridge,undefined
[13] Massachusetts 02138,undefined
[14] USA,undefined
[15] Massachusetts Institute of Technology,undefined
[16] Cambridge,undefined
[17] Massachusetts 02139,undefined
[18] USA,undefined
[19] Molecular Pathology Unit and Center for Cancer Research,undefined
[20] MGH,undefined
[21] Charlestown,undefined
[22] Massachusetts 02129,undefined
[23] USA ,undefined
[24] Harvard Medical School,undefined
[25] Boston,undefined
[26] Massachusetts 02115,undefined
[27] USA,undefined
[28] Massachusetts Institute of Technology,undefined
[29] Cambridge,undefined
[30] Massachusetts 02139,undefined
[31] USA,undefined
[32] Harvard Medical School,undefined
[33] Boston,undefined
[34] Massachusetts 02114,undefined
[35] USA,undefined
来源
Nature | 2008年 / 454卷
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摘要
DNA methylation, an important mechanism of epigenetic modification that produces different patterns of gene expression from a single DNA sequence, is vital to normal development and its malfunction can cause cancer and other abnormalities. A map of DNA methylation in embryonic stem cells, and in various cell types derived from them, has now been produced at nucleotide resolution using high-throughput bisulphite sequencing combined with single molecule-based sequencing. The map reveals specific sites in the genome where methylation changes as cells develop, for instance when embryonic stem cells mature into nerve cells. More generally, the methodology will be of value for the epigenetic profiling of cell populations relevant to developmental biology, cancer and regenerative medicine.
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页码:766 / 770
页数:4
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