The 3D-Structure of the Immunoglobulin Heavy Chain Locus

免疫球蛋白重链基因座的 3D 结构

• 批准号: 7768439
• 负责人: CORNELIS MURRE
• 金额: $ 30.59万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN DIEGO
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-03-01 至 2014-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7768439
• 关键词: Adopted; Antibody Diversity; Antibody Repertoire; Antigen Receptors; B-Cell Development; B-Lymphocytes; Biological; Biological Models; Cell Lineage; Chromatin; Chromatin Fiber; Chromatin Structure; Code; Computer Simulation; Data; Development; Elements; Family; Fiber; Frequencies; Generations; Genetic; Genome; Genomics; Goals; Heavy-Chain Immunoglobulins; Higher Order Chromatin Structure; IGH@ gene cluster; Immune response; Interphase; Invaded; Lighting; Measurement; Microscopic; Microscopy; Mitotic; Mitotic Chromosome; Molecular; Molecular Conformation; Positioning Attribute; Property; Receptor Gene; Relative (related person); Research; Resolution; Simulate; Spatial Distribution; Structure; base; insight; mammalian genome; pathogen; public health relevance; telomere; three dimensional structure

DESCRIPTION (provided by applicant): The long-range goals of the research proposed in this application are to determine at high resolution the 3D-structure of the immunoglobulin heavy chain (Igh) locus. The Igh locus is organized into distinct regions that contain multiple variable (VH), diversity (DH), joining (JH) and constant (CH) coding elements. To probe the topography of the Igh locus, we have recently determined the spatial distance distributions using 12 genomic markers that spanned the entire locus. These spatial distance distributions were compared to computer simulations of alternative chromatin arrangements. This analysis predicted that the Igh locus is organized into compartments containing clusters of loops separated by linkers. We then used computational geometry to determine the mean relative 3D-positions of the VH, DH, JH and CH elements. Briefly, the data showed that during early B cell development, the entire repertoire of VH regions (2.5 Mbp) is merged and juxtaposed to the DH elements, allowing the VH regions to encounter DHJH elements with relatively high and similar frequencies. Here we propose to continue these studies. We would describe at high resolution the average Igh locus trajectories in interphase and mitotic chromatin. We would determine the spectrum of conformations adopted by the Igh locus fiber. We would use structured illumination microscopy to visualize the Igh chromatin territories. We would characterize compartments using physical approaches. We would identify loop bases using both physical and molecular biological approaches. We would use spatial distance measurements and computational geometry to determine whether the Igh locus structure is a general feature of antigen receptor loci and eukaryotic interphase chromatin. Taken together, these studies would provide a statistical description of Igh locus structure and provide mechanistic insight into how antibody diversity is generated. PUBLIC HEALTH RELEVANCE: In previous studies we have used geometry to show how a genetic locus is organized in 3D space. The studies proposed in this application should provide insight into how the structure of the genome permits the generation of an immune response to a wide variety of invading pathogens.

描述（由申请人提供）：本申请中提出的研究的远程目标是在高分辨率下确定免疫球蛋白重链（IGH）基因座的3D结构。 IGH基因座分为有多个变量（VH），多样性（DH），加入（JH）和常数（CH）编码元素的不同区域。为了探测IGH基因座的地形，我们最近使用跨越整个基因座的12个基因组标记确定了空间距离分布。将这些空间距离分布与替代染色质排列的计算机模拟进行了比较。该分析预测，IGH基因座被组织成包含连接器分隔的环群的隔室。然后，我们使用计算几何形状来确定VH，DH，JH和CH元素的平均相对3D位置。简而言之，数据表明，在B细胞早期发育期间，VH区域（2.5 Mbp）的整个曲目合并并并置与DH元素并置，从而使VH区域遇到具有相对较高和相似频率的DHJH元素。在这里，我们建议继续这些研究。我们将在高分辨率的情况下描述相间和有丝分裂染色质中的平均IGH基因座轨迹。我们将确定IGH基因座纤维采用的构象谱。我们将使用结构化的照明显微镜来可视化IGH染色质领土。我们将使用物理方法表征隔室。我们将使用物理和分子生物学方法确定循环碱基。我们将使用空间距离测量和计算几何形状来确定IGH基因座结构是否是抗原受体基因座和真核相互相染色质的一般特征。综上所述，这些研究将提供有关IGH基因座结构的统计描述，并提供有关如何产生抗体多样性的机械洞察力。公共卫生相关性：在先前的研究中，我们已经使用几何形状展示了如何在3D空间中组织一个遗传基因座。本应用程序中提出的研究应洞悉基因组的结构如何允许对各种入侵病原体产生免疫反应。