Labeling and sequencing of 5-hmC 5-caC and 5-fC in genomic DNA - Resubmission 0

基因组 DNA 中 5-hmC、5-caC 和 5-fC 的标记和测序 - 重新提交 0

• 批准号: 8523952
• 负责人: CHUAN HE
• 金额: $ 33.84万
• 依托单位: UNIVERSITY OF CHICAGO
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-08-07 至 2015-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8523952
• 关键词: Address; Affect; Affinity; Aging; Back; Base Excision Repairs; Biological; Biological Process; Biological Sciences; Biology; Biotin; Brain; Cell Line; Cell Maintenance; Cells; Chemicals; Chemistry; Communities; Coupled; Cytosine; DNA; Deamination; Detection; Development; Dioxygen; Dioxygenases; Engineering; Ensure; Enzymes; Epigenetic Process; Exhibits; Family; Fertilization; Future; Gene Expression; Gene Expression Regulation; Genetic Code; Genome; Genomic Imprinting; Genomics; Glucose; Glucosyltransferase; Human; Information Distribution; Iron; Label; Location; Maintenance; Malignant Neoplasms; Mammalian Cell; Maps; Methods; Modification; Mus; Myelopoiesis; National Human Genome Research Institute; Nucleic Acids; Pathway interactions; Play; Positioning Attribute; Process; Proteins; Regulation; Request for Applications; Research; Resolution; Role; Site; Staging; Technology; Thymine DNA Glycosylase; Time; Tissues; Variant; X Inactivation; base; bisulfite; demethylation; embryonic stem cell; frontier; functional group; genome-wide; glycosylation; human disease; improved; mammalian genome; meetings; oxidation; single molecule; success; tool

DESCRIPTION (provided by applicant): 5-Hydroxymethylcytosine (5-hmC) is a newly identified base modification in mammalian genomic DNA. In certain tissues or cells it can accumulate to relatively high levels. Because current sequencing methods cannot differentiate 5-mC from 5-hmC, the immediate challenge is to develop robust methods to ascertain the positions of 5-hmC within the mammalian genome, a problem best addressed by adapting a new chemical labeling technology that we have invented. We show that the hydroxymethyl group of 5-hmC can be selectively labeled with chemically modified glucoses using -glucosyltransferase (GT). This glycosylation offers a strategy of installing functional groups such as biotin onto 5-hmC. In this way, we can affinity capture DNA fragments containing the modified 5-hmC and develop sequencing methods to determine the precise locations of 5-hmC. Using this new method, we have obtained the first genome-wide distribution map of 5-hmC in the mammalian genome. Building on our early successes, we propose to develop single-base resolution detection and sequencing methods to reveal the exact locations of 5-hmC in mammalian genomes. We propose different but complementary approaches in order to ensure that effective methods will be available to the biological community in the near future. The genome-wide information obtained can be used to help probe the functional roles of 5-hmC, for instance potential proteins and/or transcriptional factors that may recognize 5-hmC in specific sequence contents. We have also shown that 5-hmC can be further oxidized to 5-fC and 5-caC by the TET family enzymes. Significantly, when paired with a normal G, the 5-fC and 5-caC modification can be excised by the human thymine DNA glycosylase (TDG) without the need for base deamination. The base excision repair (BER) process effectively converts these base modifications back to C in an active demethylation process. We plan to develop selective 5-fC and 5-caC labeling and sequencing methods to obtain a genome-wide distribution map of these intriguing base modifications, respectively. In TDG-deficient cells, we believe the genome-wide distribution information of 5-fC/5-caC may reveal active demethylation sites in the specific cell stages. The proposed research will develop urgently needed tools for the PI's group and the broad biology community to study one of the most cutting-edge frontiers of life sciences research: the potential functional roles of these newly discovered DNA base modifications in epigenetics, development, and various human diseases.

描述（由申请人提供）：5-羟甲基胞嘧啶（5-hmC）是哺乳动物基因组DNA中新发现的碱基修饰。在某些组织或细胞中，它可以积累到相对较高的水平。由于目前的测序方法无法区分5-甲基mc和5-甲基mc，因此当前的挑战是开发可靠的方法来确定5-甲基mc在哺乳动物基因组中的位置，这一问题最好通过采用我们发明的新的化学标记技术来解决。我们发现5-hmC的羟基甲基可以用-葡萄糖基转移酶（GT）选择性地标记。这种糖基化提供了一种安装官能团的策略