Functional Analysis of Locus-Specific Pericentric Satellite Expression
位点特异性周中心卫星表达的功能分析
基本信息
- 批准号:9813265
- 负责人:
- 金额:$ 40.53万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2019
- 资助国家:美国
- 起止时间:2019-09-05 至 2023-08-31
- 项目状态:已结题
- 来源:
- 关键词:BindingBinding ProteinsBioinformaticsBiological AssayBiomedical ResearchCancer cell lineCell LineCell NucleusCell divisionCellsCentromereChromosomal InstabilityChromosome BreakageChromosome Fragile SitesChromosome MappingChromosomesComputer AnalysisComputer SimulationCoupledCytogenetic AnalysisCytogeneticsCytologyDNADNA SequenceDataData SetDefectElementsEngineeringFiberFluorescent in Situ HybridizationFutureGene Expression RegulationGenetic MaterialsGenetic TranscriptionGenetic studyGenomicsGoalsHuman ChromosomesHuman GenomeIn SituIndividualKnowledgeLeadLightLocationMalignant NeoplasmsMapsMass Spectrum AnalysisMethyl-CpG-Binding Protein 2MicroscopicMolecularNatureNormal CellNuclearNuclear ProteinsProteinsProteomicsPublishingRNARNA BindingRNA SequencesRegulationRepetitive SequenceReplication ErrorResearchResearch PersonnelRoleSatellite DNASequence AnalysisSeriesSiteStructureSupervisionTandem Repeat SequencesTechniquesTestingTrainingVariantbasecancer cellcareercombinatorialconstrictiondeep sequencingepigenetic regulationgene discoverygenetic regulatory proteinhuman genome sequencinginnovationinterestoverexpressionrecruitreplication stressrepositorytooltumorundergraduate student
项目摘要
PROJECT SUMMARY
The intent of this proposed research is to contribute to the basic understanding of the structure
and function of specific DNA sequences found near centromeres. Despite extensive
sequencing of the human genome, the DNA sequences residing within the centromere and the
adjacent regions (the pericentromere) are vastly unknown, due to their highly repetitive nature.
These sequences are subject to strict regulation, so they are not normally transcribed into RNA.
However, in cancer cells, HSATII, a tandemly repeated pericentric satellite sequence, is
aberrantly transcribed into RNA. In these cells, HSATII RNA accumulates in the nucleus,
adjacent to its site of transcription, where it recruits nuclear regulatory proteins. While HSATII
DNA is found on eleven different human chromosomes, only a few of these locations transcribe
HSATII RNA, suggesting that the regulation and sequence composition may vary from one
chromosome to another. Thus, a full analysis of the HSATII sequences residing on individual
human chromosomes is long overdue and merited, and promises to ultimately drive studies to
uncover the consequence of pericentric satellite transcription. In order to study tandemly
repeated sequences, a combinatorial approach is proposed to map and define HSATII variants
within individual chromosomes by integrating both in situ and in silico datasets, which will
produce a rich repository of HSATII sequences to further inform functional studies. It is
hypothesized that individual HSATII loci will harbor unique sequence variants and that
integrated sites of HSATII expression will be more prone to chromosomal breakage, resulting in
cell division defects. The hypothesis will be tested by mapping chromosome-specific HSATII
variants in the human genome (Aim 1) and by testing the role of HSATII expression in
promoting cell division defects (Aim 2). The functional effect of HSATII expression will be further
tested to determine its capacity to interact with additional nuclear regulatory proteins; this will be
accomplished by identifying the suite of proteins binding to nuclear accumulations of HSATII
RNA (Aim 3). It is anticipated that all of the proposed research will be conducted by
undergraduate students under the close supervision of the PI. Thus, the proposed project
promises to engage and train undergraduate researchers in innovative genomics, cytological
and proteomics techniques, which will propel future careers in genomics and biomedical
research.
项目总结
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Dawn M. Carone其他文献
Probing nuclear HSATII biomolecular condensates
- DOI:
10.1016/j.bpj.2023.11.1388 - 发表时间:
2024-02-08 - 期刊:
- 影响因子:
- 作者:
Thembalami Dube;Christina A. Rabeler;Dawn M. Carone - 通讯作者:
Dawn M. Carone
Demethylated HSATII DNA And HSATII RNA Foci Sequester PRC1 Demethylated HSATII DNA And HSATII RNA Foci Sequester PRC1 And MeCP2 Into Cancer-Specific Nuclear Bodies And MeCP2 Into Cancer-Specific Nuclear Bodies
去甲基化 HSATII DNA 和 HSATII RNA 焦点隔离器 PRC1 去甲基化 HSATII DNA 和 HSATII RNA 焦点隔离器 PRC1 和 MeCP2 进入癌症特异性核体,MeCP2 进入癌症特异性核体
- DOI:
- 发表时间:
2020 - 期刊:
- 影响因子:0
- 作者:
L. L. Hall;M. Byron;Dawn M. Carone - 通讯作者:
Dawn M. Carone
Centromere Conversion and Retention in Somatic Cell Hybrids
体细胞杂交体中着丝粒的转化和保留
- DOI:
10.1159/000328830 - 发表时间:
2011 - 期刊:
- 影响因子:1.7
- 作者:
Judith D. Brown;Dawn M. Carone;B. L. Flynn;C. E. Finn;E. E. Mlynarski;Rachel J. O’Neill - 通讯作者:
Rachel J. O’Neill
Human XIST RNA acts early to condense architecture which facilitates A-repeat density-dependent initiation of gene silencing
人类 XIST RNA 早期起作用以压缩结构,从而促进 A 重复密度依赖性基因沉默的启动
- DOI:
- 发表时间:
2022 - 期刊:
- 影响因子:0
- 作者:
Melvys Valledor;M. Byron;B. Dumas;Dawn M. Carone;Lisa L. Hall;J. Lawrence - 通讯作者:
J. Lawrence
The role of ncRNA in centromeres: a lesson from marsupials.
ncRNA 在着丝粒中的作用:有袋动物的教训。
- DOI:
10.1007/978-3-642-00182-6_4 - 发表时间:
2009 - 期刊:
- 影响因子:0
- 作者:
R. O’Neill;Dawn M. Carone - 通讯作者:
Dawn M. Carone
Dawn M. Carone的其他文献
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{{ truncateString('Dawn M. Carone', 18)}}的其他基金
Heterochromatin instability and misregulation of noncoding RNA in cancer
癌症中异染色质的不稳定性和非编码 RNA 的失调
- 批准号:
8391738 - 财政年份:2010
- 资助金额:
$ 40.53万 - 项目类别:
Heterochromatin instability and misregulation of noncoding RNA in cancer
癌症中异染色质的不稳定性和非编码 RNA 的失调
- 批准号:
8201093 - 财政年份:2010
- 资助金额:
$ 40.53万 - 项目类别:
Heterochromatin instability and misregulation of noncoding RNA in cancer
癌症中异染色质的不稳定性和非编码 RNA 的失调
- 批准号:
8005196 - 财政年份:2010
- 资助金额:
$ 40.53万 - 项目类别:
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