Novel regulators of skin development and Foxn1 function

皮肤发育和 Foxn1 功能的新型调节因子

• 批准号: 7576790
• 负责人: JANICE L BRISSETTE
• 金额: $ 37.87万
• 依托单位: MASSACHUSETTS GENERAL HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-03-01 至 2010-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7576790
• 关键词: Animals; Biochemical; Biological Assay; Biological Models; Cells; Charge; Complement; Complex; Congenital Alopecia; Cultured Cells; Cutaneous; DNA Binding Domain; Defect; Development; Developmental Process; Differentiation and Growth; Disease; Dissection; Environment; Epidermis; Epithelial; Epithelial Cells; Epithelium; Exhibits; Family; Gap Junctions; Gene Expression; Genetic; Genetic Screening; Goals; Growth; Growth Factor; Hair; Hair follicle structure; Hazardous Chemicals; Human; Individual; Link; Mammary gland; Mature T-Lymphocyte; Methods; Modeling; Molecular; Morphogenesis; Mus; Mutation; Nail plate; Natural regeneration; Nature; Organ; Orthologous Gene; Other Genetics; Output; Pathology; Pathway interactions; Pattern; Phenotype; Physiological; Pigmentation physiologic function; Pigments; Play; Process; Production; Property; Proteins; Recruitment Activity; Research; Rodent; Role; Screening procedure; Side; Signal Transduction; Site; Skin; Skin Pigmentation; Skin part; Structure; System; T-Cell Immunodeficiency; Testing; Thymus Gland; Transactivation; Transcription Coactivator; Ultraviolet Rays; Water; Winged Helix; Work; abstracting; base; cell type; genetic manipulation; insight; keratinocyte; melanocyte; member; novel; pathogen; programs; protein complex; repaired; research study; self-renewal; skin morphogenesis; skin regeneration; trait; transcription factor

DESCRIPTION (provided by applicant): The goal of this project is to identify the molecular partners of Foxn1 and to elucidate their contributions to skin development. Foxn1 is a transcription factor containing a winged-helix DNA-binding domain and a negatively charged transactivation domain. In rodents, the loss of Foxn1 function results in the nude phenotype, which is characterized by the abnormal morphogenesis of the skin, thymus, and mammary gland. To promote skin development, Foxn1 performs an unusual function, which was delineated by us in previous studies. Foxn1 becomes activated as epithelial cells initiate terminal differentiation in the epidermis and hair follicles. In a site-dependent manner, Foxn1 then plays up to three roles: 1) it allows its host cell to differentiate properly, 2) it stimulates the host cell's neighbors to divide, and 3) it recruits melanocytes to the host cell, thus identifying its host as a target for pigmentation. Through this combination of actions, Foxn1 enables groups of cells to work in concert and drives epithelial growth, differentiation, and pigmentation forward together. Presumably, Foxn1 itself works in concert with other factors, which provide it with information, determine its level of activity, direct it to specific targets, or function side-by-side with it in synergistic fashion. Undoubtedly, Foxn1 requires these partners for efficacy, making the partners of Foxn1 essential to the morphogenesis of the skin and other organs. During the course of this project, we will identify the partners of Foxn1 using two approaches, one genetic, the other biochemical. In the genetic approach, we will screen for mutations that modulate the activity or output of Foxn1. The screen will employ a novel model system, which we have developed for the study. In the biochemical approach, we will purify Foxn1 protein complexes from keratinocytes and dissect the individual components. Once partners are identified, we will determine how they contribute to the actions of Foxn1 and the morphogenesis of the skin. In humans, FOXN1 is conserved in sequence and function, suggesting a like conservation of partners. Accordingly, by elucidating the partnerships of Foxn1, the project should provide insight into the development of normal and diseased human skin, most especially, the disorders marked by the aberrant proliferation, differentiation, or pigmentation of epithelial cells. Project Narrative: This project will elucidate fundamental mechanisms by which the skin develops and regenerates its protective epithelial traits. Specifically, the work will delineate a genetic network that drives and coordinates the growth, differentiation, and pigmentation of the skin's external structures. In the short term, the project will explain in part how the skin produces and assembles its barrier to the environment, which provides essential protection against pathogens, hazardous chemicals, ultraviolet light, and water loss. Over the long term, the project will provide insight into how skin may be clinically generated or manipulated, thus facilitating methods for the replacement or repair of damaged and diseased skin.

描述(申请人提供)：该项目的目标是确定Foxn1的分子伙伴，并阐明它们对皮肤发育的贡献。FOXN1是一个转录因子，含有一个带翅膀的螺旋DNA结合域和一个带负电荷的反式激活结构域。在啮齿动物中，Foxn1功能的丧失导致裸露表型，其特征是皮肤、胸腺和乳腺的形态发生异常。为了促进皮肤发育，Foxn1发挥着不同寻常的功能，这一点我们在之前的研究中已经描述过了。随着上皮细胞在表皮和毛囊中启动终末分化，FOXN1被激活。然后，Foxn1以一种位置依赖的方式扮演三个角色：1)它允许宿主细胞正确分化，2)它刺激宿主细胞的邻居分裂，3)它将黑素细胞招募到宿主细胞，从而将其宿主识别为色素沉着的目标。通过这种联合作用，Foxn1使多组细胞协同工作，共同推动上皮生长、分化和色素沉着。据推测，Foxn1本身与其他因素协同工作，这些因素为它提供信息，确定它的活动水平，指导它指向特定的目标，或者以协同方式与它并肩发挥作用。毫无疑问，Foxn1需要这些伙伴来发挥功效，这使得Foxn1的伙伴对皮肤和其他器官的形态发生至关重要。在这个项目的过程中，我们将使用两种方法来确定Foxn1的合作伙伴，一种是遗传的，另一种是生化的。在遗传学方法中，我们将筛选调节Foxn1活性或产量的突变。屏幕将采用我们为这项研究开发的新型模型系统。在生化方法中，我们将从角质形成细胞中纯化Foxn1蛋白复合体，并剖析其单独的成分。一旦确定了合作伙伴，我们将确定他们如何对Foxn1的活动和皮肤的形态发生做出贡献。在人类中，FOXN1在序列和功能上是保守的，这表明伴侣之间也有类似的保守。因此，通过阐明Foxn1的伙伴关系，该项目应该能够深入了解正常和疾病人类皮肤的发育，尤其是以上皮细胞异常增殖、分化或色素沉着为标志的疾病。项目简介：该项目将阐明皮肤发育和再生其保护性上皮特征的基本机制。具体地说，这项工作将描绘一个基因网络，该网络驱动和协调皮肤外部结构的生长、分化和色素沉积。短期内，该项目将部分解释皮肤是如何产生和组装其对环境的屏障的，这将提供基本的保护，防止病原体、危险化学品、紫外线和水分损失。从长远来看，该项目将深入了解皮肤可能是如何在临床上产生或处理的，从而促进更换或修复受损和患病皮肤的方法。