REGULATION OF TRH RECEPTOR BIOSYNTHESIS

TRH 受体生物合成的调控

• 批准号: 3080736
• 负责人: THOMAS PATRICK SEGERSON
• 金额: $ 9.07万
• 依托单位: OREGON HEALTH & SCIENCE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1990
• 资助国家: 美国
• 起止时间: 1990-01-01 至 1993-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/3080736
• 关键词: Anura; autoradiography; brain mapping; complementary DNA; gel electrophoresis; gene expression; genetic library; genetic transcription; growth factor; hormone binding protein; hormone receptor; hormone regulation /control mechanism; hypothalamic pituitary axis; molecular cloning; neural transmission; neurochemistry; nucleic acid hybridization; nucleic acid probes; posttranscriptional RNA processing; protein biosynthesis; protein sequence; radiotracer; thyrotropin releasing hormone; tissue /cell culture; transfection

The applicant's training and research interests relate to the functions and control of the neuroendocrine system. The long-term objective of this proposal is to elucidate the role of the neuropeptide thyrotropin-releasing hormone (TRH) in the control of pituitary hormone secretion and neurobiology. More specifically, the aims of this proposal are to investigate the molecular events responsible for the hormonal and neuronal actions of TRH. To accomplish this aim, a complementary DNA that encodes the receptor for TRH will be cloned, using Xenopus oocyte expression system. The sequence of the protein will be deduced and compared to other neuropeptide receptor sequences. The TRH receptor cDNA will be introduced into cell lines to confirm that functional receptor is encoded by the cDNA and to investigate transcriptional and post- transcriptional levels of receptor regulation. Probes generated with the cDNA will be used to map the cells in the central nervous system which express the TRH receptor mRNA, and compare this to information about tissue binding of TRH. Similarly, these probes will be used in hybridization studies to study the regulation of endogenous TRH receptor mRNA in cell lines and in situ. A better understanding of TRH-induced cellular events should provide important information about neuronal control of pituitary function and the functional diversity of hypothalamic hormones.

申请人的培训和研究兴趣与 神经内分泌系统的功能和控制。 长期 本建议的目的是阐明 神经肽促甲状腺素释放激素（TRH）在控制 垂体激素分泌和神经生物学。 更具体地说， 这项建议的目的是研究分子事件 负责TRH的激素和神经元作用。 到 为了达到这个目的，一个编码受体的互补DNA 将TRH克隆，使用非洲爪蟾卵母细胞表达系统。 蛋白质的序列将被推导并与其他蛋白质进行比较。 神经肽受体序列。 TRH受体cDNA将被 导入细胞系，以确认功能性受体 编码的cDNA，并研究转录和后 受体调控的转录水平。 生成的探针 与cDNA将被用于绘制中枢神经系统中的细胞 表达TRH受体mRNA的系统，并将其与 TRH组织结合的信息。 同样，这些探测器 将用于杂交研究，以研究 内源性TRH受体mRNA在细胞系和原位。 更好的 对TRH诱导的细胞事件的理解应该提供 垂体功能神经元调控重要信息 以及下丘脑激素的功能多样性。