PROPAGATION OF MONKEY MODELS OF HUMAN DISEASE

人类疾病的猴子模型的传播

• 批准号: 7349502
• 负责人: DON P WOLF
• 金额: $ 7.23万
• 依托单位: HARVARD MEDICAL SCHOOL
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-05-01 至 2007-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7349502
• 关键词: PROPAGATION; MONKEY; MODELS; HUMAN; DISEASE

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. There is currently a significant need for populations of animals with specified genotypes, which can¿t be satisfied by the importation of animals from the wild, or by the identification and propagation of valuable founder animals by selective breeding. Indian-origin, rhesus macaques carrying the major histocompatability complex (MHC) class 1 allele, A*01, are particularly needed for vaccine development research. The objective of this research is to demonstrate that the assisted reproductive technologies (ARTs) can be applied to the rapid, efficient propagation of a valuable founder animal and to the production of identical twins using existing technology, thereby establishing an effective approach to satisfying animal requirements of the biomedical research community. The rationale for focusing on a homozygous, founder male is simple; all offspring produced by this animal will be Mamu-A*01 positive. Moreover, if the heterozygous carriers of the A*01 allele are used as oocyte donors, 50% of the offspring will be homozygous for the allele, creating additional founder animals.

该子项目是利用NIH/NCRR资助的中心赠款提供的资源的许多研究子项目之一。子项目和研究者（PI）可能从另一个NIH来源获得主要资金，因此可以在其他CRISP条目中表示。所列机构为中心，不一定是研究者所在机构。目前，对具有特定基因型的动物种群的需求很大，这不能通过从野生动物进口或通过选择性育种鉴定和繁殖有价值的创始动物来满足。 携带主要组织相容性复合体（MHC）1类等位基因A*01的印度恒河猴特别需要用于疫苗开发研究。本研究的目的是证明辅助生殖技术（ART）可以应用于快速，有效地繁殖一个有价值的创始人动物和生产的同卵双胞胎使用现有的技术，从而建立一个有效的方法来满足生物医学研究界的动物要求。关注纯合的创始雄性的基本原理很简单;该动物产生的所有后代均为Mamu-A*01阳性。此外，如果使用A*01等位基因的杂合携带者作为卵母细胞供体，则50%的后代将是等位基因纯合的，从而产生额外的创始动物。