Regulation of cell and organ size in vivo
Regulation of cell and organ size in vivo
批准号:
8136621
负责人:
Iswar K. Hariharan
金额:
$29.52万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-08-01 至 2013-08-31
关键词:
AddressApoptosisBiological AssayBirthCell CommunicationCell Cycle ProgressionCell SurvivalCell divisionCellsChromosome ArmChromosomesDevelopmentDiseaseDrosophila eyeDrosophila genusEyeFundingGenesGeneticGenetic ScreeningGenotypeGoalsGrantGrowthHealthHistocompatibility TestingIndividualLaboratoriesMAP Kinase GeneMalignant NeoplasmsMammalsMutateMutationOpen Reading FramesOrganOrgan SizeOrganismPathway interactionsProcessPublishingRegulation of Cell SizeRoleScreening procedureSignal TransductionTissuesWritingX Chromosomearmcell growth regulationcell typedesigngene functionimaginal discimprovedin vivoinsightkillingsmutantnovelresearch studytranscription factortumor
中文摘要
描述(由申请人提供):本项目旨在了解体内组织生长和器官大小的遗传途径。我们实验室以前的研究利用了一种筛选方法,该方法利用发育中的果蝇眼睛中产生的遗传嵌合体来识别导致组织过度生长的突变。在筛选中发现的许多突变已经在该补助金的以前资助期间进行了表征。在该提案中,前两个特定目的详细描述了表征X染色体筛选中鉴定的两个基因座的实验:ovo和HK 115。目的1描述了一种用于鉴定在HK 115突变体中突变的开放阅读框的策略,以及确定HK 115如何调节组织生长和凋亡的实验。目的2概述了表征卵蛋白(编码转录因子)调节生长和细胞周期进程的途径的研究。目的3和4解决了一种被称为细胞竞争的知之甚少的现象,通过这种现象,细胞能够杀死生长较慢的相邻细胞。已经开发了一种新的筛选方法来识别超级竞争者-使突变细胞能够杀死其野生型邻居的突变。在筛选中鉴定了碎屑中的突变,碎屑是顶基极性的调节剂。目的3描述了一种方法来确定碎屑如何与细胞竞争。目标4包括一个广泛的策略,包括一个新的遗传筛选,用于识别和表征调节细胞竞争的其他基因。这些研究可能会提供有价值的见解,如何在发展过程中的生长调节,以及在肿瘤的发展过程中发生的生长异常。公共卫生相关性:细胞生长、细胞分裂和存活的精确调节是生物体正常发育所必需的。这些过程的干扰可能导致出生异常和癌症。该提案描述了一种遗传方法,使用果蝇,以提高我们对调节组织生长机制的理解。
英文摘要
DESCRIPTION (provided by applicant): This project is aimed at understanding the genetic pathways that tissue growth and organ size in vivo. Previous studies in our laboratory have utilized a screen that utilizes genetic mosaics generated in the developing Drosophila eye to identify mutations that result in tissue overgrowth. Many of the mutations that have been identified in the screen have been characterized during previous funding periods of this grant. In this proposal, the first two Specific Aims detail experiments to characterize two loci that were identified in the screen of the X-chromosome: ovo and HK115. Aim 1 describes a strategy for identifying the open reading frame that is mutated in the HK115 mutants and experiments to determine how HK115 regulates tissue growth and apoptosis. Aim 2 outlines studies for characterizing the pathway by which ovo, which encodes a transcription factor regulates growth and cell cycle progression. Aims 3 and 4 address a poorly understood phenomenon known as cell competition by which cells are able to kill adjacent cells that grow more slowly. A novel screen has been developed to identify supercompetitors - mutations that enable mutant cells to kill their wild-type neighbors. Mutations in crumbs, a regulator of apicobasal polarity were identified in the screen. Aim 3 describes an approach to determine how crumbs functions with respect to cell competition. Aim 4 consists of a broad strategy, including a new genetic screen, for identifying and characterizing additional genes that regulate cell competition. These studies are likely to provide valuable insights into how growth is regulated during development as well as the growth abnormalities that occur during the development of tumors. PUBLIC HEALTH RELEVANCE: The precise regulation of cell growth, cell division and survival are necessary for the proper development of an organism. Perturbations of these processes can result in birth abnormalities and cancer. This proposal describes a genetic approach, using the fruit fly, to improve our understanding the mechanisms that regulate tissue growth.
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