MOUSE MODELS OF ALBINISM

白化病小鼠模型

• 批准号: 2372648
• 负责人: MURRAY H BRILLIANT
• 金额: $ 27.08万
• 依托单位: RESEARCH INST OF FOX CHASE CAN CTR
• 依托单位国家: 美国
• 财政年份: 1997
• 资助国家: 美国
• 起止时间: 1997-01-01 至 1997-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/2372648
• 关键词: P glycoprotein; albinism; cell biology; disease /disorder model; electron microscopy; gene expression; genetic mapping; immunofluorescence technique; laboratory mouse; melanocyte; model design /development; molecular cloning; phenotype; pigmentation disorders; platelet disorder; protein structure function

Human deficiencies of pigment formation, including oculocutaneous albinism are common genetic abnormalities with severe cutaneous and optic system effects. A reduction of melanin production in the skin results in a marked sensitivity to ultraviolet radiation and a predisposition of skin cancer. Reduction of melanin in the eye during development is associated with life- long nystagmus, foveal hypoplasia with reduced visual acuity, and abnormal routing of the neural connections from the retina to the brain, resulting in strabismus and loss of binocular vision. The clinical characteristics of six or more types of human oculocutaneous albinism have been described, and it is now clear that some of these result from different mutations at a single locus (allele heterogeneity), while others result from mutations at different loci (locus heterogeneity). The overall aims of this project are to investigate the clinical, ophthalmological, hematological, epidemiological, biochemical and molecular features of normal and abnormal human pigment formation, particularly oculocutaneous albinism. These studies will provide information which we hope will lead to methods of accurate diagnosis, therapy, and family counseling, so that these genetic diseases can be prevented, treated, or ameliorated. Four projects and a core facility will be utilized for this work. Project 1 will analyze the molecular and the biochemical characteristics of the different types of tyrosinase-related oculocutaneous albinism. Project 2 will analyze the defects in regulatory mechanisms and membranes in platelets and blood cells in patients with hypopigmentation, including the Hermansky-Pudlak syndrome. Project 3 will analyze the human correlate of the mouse pink-eyed dilution gene and will look for a type of human oculocutaneous hypopigmentation that is associated with changes in this gene. Project 4 will analyze the biology of the melanocyte int he different types of human oculocutaneous albinism. The core facility will provide support for the ophthalmologic evaluation of the patients seen in the different projects, for the biophysical analysis of the structure and function of the melanin isolated in the different projects, and for the development of a transgenic mouse model of pigmentation that can be used in the analysis of the effects of melanin on the development of the optic and auditory system.

人类色素形成不足，包括眼皮肤白化病 是常见的遗传异常，有严重的皮肤和视觉系统 效果。皮肤中黑色素生成的减少会导致明显的 对紫外线的敏感性和皮肤癌的易感性。 眼睛发育过程中黑色素的减少与生命有关- 长时间眼球震颤，中心凹发育不良，视力下降，异常 从视网膜到大脑的神经连接的路由，结果 斜视和双眼视觉丧失。临床特点分析 已经描述了六种或更多种类型的人类眼皮肤白化病， 现在很清楚的是，其中一些是由不同的突变引起的 单个基因座(等位基因异质性)，而其他基因座则由突变引起 在不同的基因座(基因座异质性)。 这个项目的总体目标是调查临床， 眼科学、血液学、流行病学、生化和分子 人体正常和异常色素形成的特点，特别是 眼皮肤白化病。这些研究将提供信息，我们将 希望将导致准确的诊断、治疗和家庭方法 咨询，以便这些遗传病可以被预防、治疗或 改善了。四个项目和一个核心设施将用于这一点 工作。 项目1将分析分子和生化特征 不同类型的酪氨酸酶相关性眼皮肤白化病。项目 2将分析在调节机制和膜方面的缺陷 色素减退患者的血小板和血细胞，包括 赫尔曼斯基-普德拉克综合征。项目3将分析人类与 小鼠粉色眼睛的稀释基因，并将寻找一种人类 与这一变化相关的眼皮肤色素减退 吉恩。项目4将分析黑素细胞的生物学特性。 不同类型的人类眼皮肤白化病。核心设施将 为患者的眼科评估提供支持 不同的项目，用于结构的生物物理分析和 在不同项目中分离的黑色素的功能，以及对于 一种转基因小鼠色素沉着模型的研制 黑色素对视神经发育的影响分析 听觉系统。