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Genetics of Alopecia Areata in the C3H/HeJ Mouse

C3H/HeJ 小鼠斑秃的遗传学

基本信息

批准号：
8290409
负责人：
JOHN Paul SUNDBERG
金额：
$ 38.12万
依托单位：
JACKSON LABORATORY
依托单位国家：
美国
项目类别：
财政年份：
2010
资助国家：
美国
起止时间：
2010-07-10 至 2015-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8290409
关键词：
A/J Mouse Adult Affect Aging Alleles Alopecia Areata Alternative Splicing Autoimmune Diseases Autoimmune Process C3H/HeJ Mouse Candidate Disease Gene Cells Chromosome Mapping Clinical Code Complex Computer software Congenic Strain Consomic Strain Data Databases Diagnosis Diagnostic Diet Disease Disease Progression Drug Delivery Systems Failure Future Gene Expression General Population Genes Genetic Genetic Crosses Genetic Variation Genomics Genotype Hair Hair follicle structure Haplotypes Hereditary Disease Human Human Genetics Immune Inbred Strain Intervention Trial Knock-out Lead Link Maps Mediating Minor Modeling Molecular Mouse Strains Mus Mutate Northern Blotting Nucleic Acid Regulatory Sequences Pathogenesis Pathway interactions Patients Pharmaceutical Preparations Phase Phenotype Polygenic Traits Population Predisposition Psychological Stress Public Health Quantitative Trait Loci Rattus Regulator Genes Resistance Resources Screening procedure Severities Severity of illness Structural Protein Suicide Technology Teenagers Testing Time Transcript Trauma Vitamin A Western Blotting Work aged analytical method base design drug efficacy genetic linkage girls human disease mouse model mutant novel prototype public health relevance repository skin disorder success systemic autoimmune disease tool

项目摘要

DESCRIPTION (provided by applicant): Alopecia areata (AA) is a disfiguring human autoimmune skin disease with a complex genetic basis that targets hair follicles in the actively growing anagen phase and is often associated with other systemic autoimmune diseases. Psychogenic trauma due to hair loss, particularly for teen-aged girls, can be so serious as to lead to suicide. AA can affect up to 2% of the general population at some time during their lives (6,000,000 US citizens). C3H/HeJ mice spontaneously develop AA and, like in humans, this is a very complex polygenic disease with susceptibility loci in common with both human AA patients and the rat AA model. Our previous hypothesis was that AA was due to the interaction of immune-regulatory genes affecting pathways that can be identified by systematic analysis of gene expression levels within each quantitative trait locus (QTL) interval previously identified. While this idea remains viable, we have now identified genes within these QTLs which go beyond immune regulatory genes towards explaining many of the key issues in the pathogenesis of this extremely complicated disease. Gene array data from a cross sectional AA study (completed, including mice with spontaneous disease), when combined with quantitative real time RT PCR (QPCR) for all genes within each of the 4 AA quantitative trait loci (QTLs) and haplotype mapping data based on total genomic sequencing (Sanger draft sequences), will be used to identify numerous candidate genes involved in the pathogenesis of AA that will allow for prioritization of molecular pathways for future intervention trials. To validate this work we will use a prototype mouse AA-specific QPCR 384 gene array (completed) to provide expression based phenotyping capabilities, adding Expression-based Quantitative Trait Locus (EQTL) analytical methods to analyze new genetic crosses. By evaluating mice that develop AA in the separate aging of Collaborative Cross mice (nearly 200 carefully genotyped novel mouse strains that provide expanded genetic diversity), we will identify new QTLs and refine the known QTLs. In so doing, we will reduce the mouse genetic intervals, find and test candidate genes, identify new loci, and validate our new molecular tools that will eventually add value to drug and diagnostic screening approaches. Discoveries using this mouse model continue to contribute to a better understanding and treatment options for human AA, especially since recent human genetic linkage studies found corresponding genetic intervals to those in our mouse model. PUBLIC HEALTH RELEVANCE: Alopecia areata is a relatively common (up to 2% of the population, 6,000,000+ people, during their lifetime) autoimmune disease that causes severe psychological stress. Our mouse model provides a comprehensive understanding of this extremely complex genetic disease. Over 38 genes are dysregulated in the major quantitative trait locus and, with these data, plus that from the 3 minor loci, the major molecular network has been defined that leads to this cell mediated autoimmune skin disease. One of the major structural proteins in the hair was identified that is downregulated resulting in fragility and breakage, the clinical presentation of alopecia areata. Environmental (vitamin A levels in the diet) effects on disease severity were first identified in the mouse and recently confirmed in human patients. Refining and expanding these observations will help us understand the genetic basis of alopecia areata. Changes in gene networks associated with alopecia areata disease progression and success or failure of drug efficacy screening studies will provide new tools to accurately diagnose the human disease and predict optimal treatment regiments.

描述（由申请人提供）：