首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Use of yeast artificial chromosomes (YACs) in studies of mammalian development: production of beta-globin locus YAC mice carrying human globin developmental mutants.
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Use of yeast artificial chromosomes (YACs) in studies of mammalian development: production of beta-globin locus YAC mice carrying human globin developmental mutants.

机译:酵母人工染色体(YAC)在哺乳动物发育研究中的用途:生产β-球蛋白基因座携带人球蛋白发育突变体的YAC小鼠。

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摘要

To test whether yeast artificial chromosomes (YACs) can be used in the investigation of mammalian development, we analyzed the phenotypes of transgenic mice carrying two types of beta-globin locus YAC developmental mutants: (i) mice carrying a G-->A transition at position -117 of the A gamma gene, which is responsible for the Greek A gamma form of hereditary persistence of fetal hemoglobin (HPFH), and (ii) beta-globin locus YAC transgenic lines carrying delta- and beta-globin gene deletions with 5' breakpoints similar to those of deletional HPFH and delta beta-thalassemia syndromes. The mice carrying the -117 A gamma G-->A mutation displayed a delayed gamma- to beta-globin gene switch and continued to express A gamma-globin chains in the adult stage of development as expected for carriers of Greek HPFH, indicating that the YAC/transgenic mouse system allows the analysis of the developmental role of cis-acting motifs. The analysis of mice carrying 3' deletions first provided evidence in support of the hypothesis that imported enhancers are responsible for the phenotypes of deletional HPFH and second indicated that autonomous silencing is the primary mechanism for turning off the gamma-globin genes in the adult. Collectively, our results suggest that transgenic mice carrying YAC mutations provide a useful model for the analysis of the control of gene expression during development.
机译:为了测试酵母人工染色体(YACs)是否可用于研究哺乳动物的发育,我们分析了携带两种类型的β-球蛋白基因座YAC发育突变体的转基因小鼠的表型:(i)携带G-> A过渡的小鼠位于A伽玛基因的-117位置,该基因负责胎儿血红蛋白(HPFH)的希腊A伽玛形式的遗传持久性,以及(ii)携带δ-和β-珠蛋白基因缺失的β-珠蛋白基因座YAC转基因品系5'断点类似于删除型HPFH和δ-地中海贫血综合征。携带-117 A gamma G-> A突变的小鼠显示出延迟的gamma-珠蛋白基因转换,并在成年发育阶段继续表达A gamma-珠蛋白链,正如希腊HPFH携带者所预期的那样,这表明YAC /转基因小鼠系统可以分析顺式作用基序的发育作用。对携带3'缺失的小鼠的分析首先提供了证据,支持以下假设:进口的增强子是造成HPFH缺失的表型的原因,其次表明,自主沉默是关闭成体中γ-珠蛋白基因的主要机制。总的来说,我们的结果表明,携带YAC突变的转基因小鼠为分析发育过程中的基因表达提供了有用的模型。

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