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The three-dimensional structure of the immunoglobulin heavy chain locus: Implications for long-range genomic interactions.

机译:免疫球蛋白重链基因座的三维结构:对长距离基因组相互作用的影响。

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摘要

The immunoglobulin heavy chain (Igh) locus is organized into distinct regions that encode multiple variable (VH), diversity (DH), joining (JH) and constant (CH) gene segments. DNA recombination takes place between the VH, DH and JH segments at the Igh locus in developing B cells. The locus undergoes large-scale contraction to facilitate this recombination. However, its structural organization is unknown. It is likely that the structural organization plays a role in this process.;By simultaneously visualizing three subregions of the Igh locus using 3D uorescence in-situ hybridization, we show that looping of the distal VH segments to the CH segments is observable in pro-B cells. This looping occurs at a significantly higher frequency in pro-B cells compared to CD8+ T cells. This indicated that there is a structural reorganization of the locus and not just a simple contraction of the chromatin fiber.;To decipher the topology of the locus, 12 genomic markers were used that spanned the entire locus. Spatial distance distributions between different combinations of these markers were determined and compared to computer simulations of different models of chromatin structure. These comparisons revealed that the data agreed with a topology that predicted higher order organization of the chromatin fiber into multiple subcompartments connected by linkers (Multi-Loop Subcompartment model). Compartmentalization of the locus was visualized by labeling the entire locus with hybridization markers. Relative locations of the different Igh sub-regions in 3D space were determined using a trilateration technique. Striking conformational changes can be seen between pre-pro-B and pro-B cells, when the locus transitions from a de-contracted to a contracted state.;The implications of the higher order organization of the locus on long-range genomic interactions are discussed. It is evident that the higher order organization is necessary for promoting long-range genomic interactions that would facilitate V(D)J recombination at the Igh locus. In absence of higher order organization, the expected frequency of interactions are much lesser.
机译:免疫球蛋白重链(Igh)基因座被组织成不同的区域,这些区域编码多个可变(VH),多样性(DH),连接(JH)和恒定(CH)基因区段。 DNA重组发生在发育中的B细胞中Igh基因座的VH,DH和JH段之间。该基因座经历大规模收缩以促进这种重组。但是,其结构组织是未知的。通过在3D荧光原位杂交同时可视化Igh基因座的三个子区域,我们显示了远端VH节段到CH节段的循环是可观察到的。 B细胞。与CD8 + T细胞相比,该循环在pro-B细胞中以明显更高的频率发生。这表明存在基因座的结构重组,而不仅是染色质纤维的简单收缩。为了破译基因座的拓扑结构,使用了横跨整个基因座的12个基因组标记。确定这些标记物的不同组合之间的空间距离分布,并将其与染色质结构不同模型的计算机模拟进行比较。这些比较表明,数据与拓扑结构相吻合,该拓扑结构可预测染色质纤维以更高的顺序组织成多个通过连接子连接的子隔间(多环子隔间模型)。通过用杂交标记物标记整个基因座,可以看到基因座的区室化。使用三边测量技术确定3D空间中不同Igh子区域的相对位置。当基因座从收缩状态转变为收缩状态时,在前B细胞和前B细胞之间可以看到惊人的构象变化。该基因座的高阶组织对远程基因组相互作用的影响是讨论过。显然,高阶组织对于促进长距离基因组相互作用是必要的,这将促进Igh位点的V(D)J重组。在没有更高层次组织的情况下,预期的交互频率要小得多。

著录项

  • 作者

    Jhunjhunwala, Suchit.;

  • 作者单位

    University of California, San Diego.;

  • 授予单位 University of California, San Diego.;
  • 学科 Molecular biology.;Bioinformatics.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 144 p.
  • 总页数 144
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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