The role of YY1 in constitutive and inducible DNA loop formation

YY1 在组成型和诱导型 DNA 环形成中的作用

• 批准号: 9126585
• 负责人: Michael Lee Atchison
• 金额: $ 30.4万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-09-01 至 2018-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9126585
• 关键词: Address; Antibody Repertoire; B-Lymphocytes; Binding; CRISPR/Cas technology; ChIP-seq; Chromatin Loop; Complex; DNA; DNA Binding; DNA Sequence; Data; Defect; Development; Developmental Gene Expression Regulation; Disease; Enhancers; Gene Rearrangement; Genetic Transcription; Genome; Health; Histones; Immune; Immunoglobulin Class Switching; Immunoglobulin Genes; Immunoglobulin Switch Recombination; Immunoglobulins; Knock-out; Lamins; Lead; Lymphomagenesis; Mediating; Molecular; Molecular Cloning; Mus; Phospho-Specific Antibodies; Play; Polycomb; Post-Translational Protein Processing; Process; Proteins; Publishing; RNA Interference; Role; Site; Splenocyte; Staging; System; Testing; Tissues; Transcript; Untranslated RNA; Work; YY1 Transcription Factor; base; cohesin; condensin; cytokine; experience; immune function; innovation; insight; knock-down; mutant; novel; protein protein interaction; reconstitution; stem cell biology

DESCRIPTION: Long-distance DNA interactions are critically involved in developmental regulation of gene expression, stem cell biology, and immune functions. The immunoglobulin (Ig) genes best exemplify the importance of long- distance DNA interactions as somatic rearrangement of these genes requires linkage of DNA sequences separated by as much as 3 megabases. Similarly, Ig class switch recombination (CSR) requires formation of both constitutive and cytokine-inducible loops within switch region DNA sequences, and interactions between enhancer sequences (E� and 3'RR enhancers) that are separated by 200 kb. Although many long-distance loops have been identified at the Ig loci, the molecular mechanisms that control their formation remain unclear. We recently published the novel observation that the transcription factor YY1 controls antibody repertoires at the Ig� locus and physically interacts with condensin, cohesin, and Polycomb Group (PcG) proteins, all of which are involved in long-distance DNA loop formation. Moreover, co-localization of YY1 with these proteins within the Ig� locus suggests that YY1 controls long-distance DNA interactions. In further support, recent evidence shows that YY1 plays critical roles in long-distance DNA interactions at the IgH, Ig�, and the Th2 cytokine loci. Notably, our preliminary data demonstrate that YY1 conditional knock-out reduces CSR and dramatically ablates long-distance DNA loops required for CSR. Based on our combined data, we hypothesize that YY1 developmentally regulates CSR by both constitutive and cytokine inducible binding to DNA, and subsequent recruitment of proteins (condensin, cohesin, PcG proteins, etc.) required for long-distance DNA loop formation. We are uniquely poised to test this hypothesis in our recently developed powerful and innovative YY1 conditional knockout/reconstitution primary ex vivo splenoctye system. As YY1 is a ubiquitous protein, its role in DNA loop formation must be regulated tissue-specifically and B cell stage-specifically by either post-translational modification, or by developmentally regulated protein-protein interactions. Therefore, in addition to determining how YY1 contributes to long-distance DNA loop formation, we will identify the YY1- interacting proteins required for loop formation, and characterize the developmental and inducible mechanisms governing this process. Defining the role of YY1 in CSR will provide foundational insights into humoral immune mechanisms, and may lead to new paradigms of long-distance DNA interactions, and the translocations that drive lymphomagenesis. We have over two decades experience with YY1 function and have developed numerous unique molecular clones and genetically modified mouse lines to address YY1 function in DNA loop formation.

产品说明：长距离DNA相互作用在基因表达、干细胞生物学和免疫功能的发育调控中起着关键作用。免疫球蛋白（IG）基因最能说明长距离DNA相互作用的重要性，因为这些基因的体细胞重排需要间隔多达3兆碱基的DNA序列的连接.类似地，IG类转换重组（CSR）需要在转换区DNA序列内形成组成型和组氨酸诱导型环，以及相隔200 kb的增强子序列（E ′和3 ′ RR增强子）之间的相互作用。尽管在IG位点发现了许多长距离环，但控制其形成的分子机制仍不清楚。我们最近发表了一项新的观察结果，即转录因子YY 1控制IG β位点的抗体库，并与凝聚素、粘附素和多梳组（PcG）蛋白发生物理相互作用，所有这些蛋白都参与长距离DNA环的形成。此外，YY 1与这些蛋白质在IG β基因座内的共定位表明YY 1控制长距离DNA相互作用。最近的证据进一步支持YY 1在IgH、IG β和Th 2细胞因子位点的长距离DNA相互作用中起关键作用。值得注意的是，我们的初步数据表明，YY 1条件性敲除减少了CSR，并显着消融了CSR所需的长距离DNA环。基于我们的综合数据，我们假设YY 1通过与DNA的组成性和细胞因子诱导性结合以及随后的蛋白质（凝聚素、粘附素、PcG蛋白等）募集来发育性地调节CSR。长距离DNA环形成所需的蛋白质。我们在最近开发的强大和创新的YY 1条件性敲除/重建原发性离体脾细胞系统中独特地准备检验这一假设。由于YY 1是一种普遍存在的蛋白质，其在DNA环形成中的作用必须通过翻译后修饰或发育调节的蛋白质-蛋白质相互作用来进行组织特异性和B细胞阶段特异性调节。因此，除了确定YY 1如何有助于长距离DNA环的形成，我们将确定YY 1相互作用的蛋白质所需的环的形成，并表征发育和诱导机制，管理这个过程。确定YY 1在CSR中的作用将为体液免疫机制提供基础性见解，并可能导致长距离DNA相互作用的新范例，以及驱动淋巴瘤发生的易位。我们在YY 1功能方面拥有超过二十年的经验，并开发了许多独特的分子克隆和转基因小鼠品系，以解决YY 1在DNA环形成中的功能。