权益分类	功能权益	普通用户	{{item.name}}会员
{{category.name}}	{{benefitItem.name}}

Regulators and Regulation of MHC class II genes

MHC II 类基因的调控者和调控

基本信息

批准号：
7163465
负责人：
JOSEPH D FONTES
金额：
$ 24.39万
依托单位：
UNIVERSITY OF KANSAS MEDICAL CENTER
依托单位国家：
美国
项目类别：
财政年份：
2005
资助国家：
美国
起止时间：
2005-04-15 至 2009-12-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7163465
关键词：
Address Affect Autoantigens Autoimmune Diseases Binding Binding Proteins Biochemical Genetics Boxing C-Terminal Binding Protein 1 Catalytic Domain Cell Line Cells Chromatin Remodeling Factor Chromatin Structure Class Code Complementary DNA Complex DNA DNA Binding DNA Sequence Ensure Enzymes Gene Expression Gene Expression Regulation Genes Genetic Techniques Genetic Transcription Histocompatibility Antigens Class II Histone Code Histones Immune Immune response Immune system Infection Laboratories Location MHC Class I Genes MHC Class II Genes Mediating Modification Molecular Protein Binding Proteins RFX regulatory factor RNA Interference Recruitment Activity Regulation Research Personnel Role SLC26A3 gene Structure Techniques Testing Time Trans-Activators Transcription Regulatory Protein Transcriptional Activation Transcriptional Regulation Work Zinc Fingers base brahma brahma protein cell type chromatin remodeling genetic regulatory protein hSWI/SNF human disease insight novel programs promoter research study transcription factor

项目摘要

DESCRIPTION (provided by applicant): Major histocompatibility complex class II gene transcription is tightly regulated, to ensure effective immune system activity. Inappropriate expression of these genes can result in autoimmune disease. Understanding the molecular mechanisms of MHC II transcription may allow the creation of novel immune based therapies for many human diseases. Gene-specific transcription factors assemble at MHC II promoters, to initiate transcription. Of critical importance are the heterotrimeric regulatory factors X (RFX) complex and the class II trans-activator protein (CUTA). CIITA, and one subunit of RFX known as RFXAP, both interact with a chromatin remodeling factor, brahma related gene-1 (BRG1). Whether the RFXAP-BRG1 interaction leads to chromatin remodeling appears to be dependent on cell-type. To explain this observation, it is hypothesized that the appropriate histone modifications must be present at MHC II promoters for RFXAPBRG1 to effectively remodel chromatin. In specific aim 1, histone modifications, and the enzymes responsible for those modifications, will be characterized at MHC II promoters. The observed modifications will be correlated with the ability of RFXAP-BRG1 and CIITA-BRG1 interactions to remodel chromatin. Results will provide insight into cell-type specific regulatory mechanisms controlling MHC II transcription. In the specific aim 2, a new transcriptional regulatory protein for MHC class II genes will be characterized. A cDNA that codes for a novel protein that binds the C-terminus of CIITA was recently cloned. This zinc finger protein is called CCB1. Over-expression of CCB1 results in super-activation of MHC class I and class II genes by CIITA. It is likely that CCB1 binds DNA, and may in fact interact with the W-box of MHC promoters. Employing biochemical and genetic techniques, the manner in which CCB1 alters MHC class II transcription, and CIITA activity, will be addressed. In addition, a broader role for CCB1 in gene regulation, beyond MHC genes, will be explored.

描述（由申请方提供）：主要组织相容性复合体II类基因转录受到严格调控，以确保有效的免疫系统活性。这些基因的不适当表达可导致自身免疫性疾病。了解MHC II转录的分子机制可能会为许多人类疾病创造新的基于免疫的疗法。基因特异性转录因子在MHC II启动子处组装以启动转录。至关重要的是异源三聚体调节因子X（RFX）复合物和II类反式激活蛋白（CUTA）。CIITA和RFX的一个亚基RFXAP都与染色质重塑因子brahma相关基因1（BRG 1）相互作用。RFXAP-BRG 1相互作用是否导致染色质重塑似乎取决于细胞类型。为了解释这一观察结果，假设适当的组蛋白修饰必须存在于RFXAPBRG 1的MHC II启动子处，以有效地重塑染色质。在具体目标1中，将在MHC II启动子处表征组蛋白修饰和负责这些修饰的酶。观察到的修饰将与RFXAP-BRG 1和CIITA-BRG 1相互作用重塑染色质的能力相关。结果将提供深入了解细胞类型特异性调控机制控制MHC II转录。在具体目标2中，将表征针对MHC II类基因的新的转录调节蛋白。最近克隆了一种编码结合CIITA C-末端的新蛋白的cDNA。这种锌指蛋白被称为CCB 1。CCB 1的过表达导致CIITA对MHC I类和II类基因的超活化。CCB 1很可能与DNA结合，并可能实际上与MHC启动子的W盒相互作用。利用生物化学和遗传技术，将解决CCB 1改变MHC II类转录和CIITA活性的方式。此外，CCB 1在MHC基因以外的基因调控中的更广泛作用将被探索。