PROSTATE DEVELOPMENT USING CRE RECOMBINASE

使用 CRE 重组酶促进前列腺发育

• 批准号: 6311099
• 负责人: Henry M Sucov
• 金额: $ 16.34万
• 依托单位: UNIVERSITY OF SOUTHERN CALIFORNIA
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-09-30 至 2002-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6311099
• 关键词: gene expression; gene mutation; genetic recombination; genetic regulation; genetically modified animals; histogenesis; laboratory mouse; prostate; recombinase; reporter genes; transfection

A new transgenic mouse model (called PB-cre), in which cre recombinase is expressed specifically in the male prostate under the control of the prostate-specific probasin promoter, has been derived for the study of prostate development and cancer. In this R2l application, we first propose to characterize the expression pattern of this transgene and to define the onset and extent of recombination over time of conditional genes. We then propose to selectively mutate the retinoid receptor RXR alpha: gene in prostatic epithelium in normal mice and in mice genetically disposed to prostatic epithelial dysplasia. Specific Aim 1: To define the pattern of recombination driven by the PB- cre transgene. A comprehensive description of the timing and extent of recombination as driven by this transgene will be obtained by crossing to the well-characterized conditional reporter gene ROSA26R (R26R). Specific Aim 2: To selectively mutate the RXR alpha: gene in prostate epithelium. Abundant prior and new evidence presented in this proposal implicate a role for retinoids and retinoid receptors, particularly RXR alpha:, in the derivation and maintenance of prostatic epithelium and in the progression of prostate cancer. We will cross the crc-expressing transgene with a conditional allele of RXR alpha:, and evaluate the nature and extent of morphological alterations in the prostatic epithelium. We will also cross the conditional mutation of RXR alpha: into the Nkx3. l knockout mouse model to evaluate the extent to which RXR alpha: modulates the initiation and progression of prostate dysplasia and cancer.

一种新的转基因小鼠模型（称为PB-cre），其中cre重组酶在前列腺特异性probasin启动子的控制下在男性前列腺中特异性表达，已被用于前列腺发育和癌症的研究。在该R21申请中，我们首先提出表征该转基因的表达模式，并定义条件基因随时间重组的开始和程度。然后，我们建议选择性突变的维甲酸受体RXR α：基因在前列腺上皮细胞在正常小鼠和遗传倾向于前列腺上皮发育不良的小鼠。具体目的1：确定PB-cre转基因驱动的重组模式.通过与充分表征的条件性报告基因ROSA 26 R（R26 R）杂交，将获得由该转基因驱动的重组的时间和程度的全面描述。具体目标2：选择性突变前列腺上皮中的RXR α：基因。该提案中提出的大量先前和新证据表明，类维生素A和类维生素A受体，特别是RXR α：，在前列腺上皮的衍生和维持以及前列腺癌的进展中发挥作用。我们将crc表达转基因与RXR α的条件等位基因杂交，并评估前列腺上皮细胞形态学改变的性质和程度。我们还将RXR alpha的条件突变：交叉到Nkx 3中。1敲除小鼠模型，以评估RXR α：调节前列腺发育不良和癌症的起始和进展的程度。