用酵母双杂交方法鉴定肿瘤抑制因子PTEN的新结合伙伴。

Eksperimental'naia onkologiia Pub Date : 2004-03-01
Olena Gorbenko, Vitaliy Kuznetsov, Olexandr Kukharenko, Alexandr Zhyvoloup, Ganna Panasyuk, Ivan Nemazanyy, Valeriy Filonenko, Ivan Gout
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引用次数: 0

摘要

目的:寻找新的pten结合伙伴。方法:采用酵母双杂交筛选技术。构建了一组诱饵结构体,包含PTEN的c端结构域、全长PTEN、活化和磷酸酶死亡突变体。根据双工A系统的标准方案测试了lexa融合诱饵的表达、核定位和自激活电位。从结肠癌、HeLa和小鼠胚胎中筛选CDNA文库。分离的阳性克隆进一步通过配对试验进行分析,并通过DNA自动测序和数据库检索进行鉴定。结果:对PTEN全长和c端结构域cDNA文库进行广泛筛选,鉴定出43个阳性克隆,并在配种实验中得到证实。序列分析表明,两个克隆编码脂肪细胞增强子结合蛋白1 (adicyte Enhancer Binding Protein 1, AEBP1)。结论:我们的数据表明,PTEN和AEBP1的相互作用分别由它们的c端和n端结构域介导。目前正在研究PTEN-AEBP1相互作用的功能重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of a novel binding partners for tumor suppressor PTEN by a yeast two-hybrid approach.

Aim: To identify novel PTEN-binding partners.

Methods: The technique of yeast two-hybrid screening was used in this study. A panel of bait constructs was created, containing the C-terminal domain of PTEN, full length PTEN, activated and phosphatase-dead mutants. The expression of LexA-fused baits, their nuclear localization and autoactivation potential were tested according to the standard protocol of Duplex A system. CDNA libraries from Colon Cancer, HeLa and Mouse Embryo were screened with two selected bait constructs. Isolated positive clones were further analysed by mating assay and identified by automated DNA sequencing and database searching.

Results: Extensive screening of cDNA libraries with the full length and the C-terminal domain of PTEN led to the identification of 43 positive clones, which were confirmed in mating assay. Sequence analysis indicated that two clones encode AEBP1 (Adipocyte Enhancer Binding Protein 1).

Conclusion: Our data indicate that the interaction between PTEN and AEBP1 is mediated by their C-terminal and N-terminal domains, respectively. The functional importance of PTEN-AEBP1 interaction is currently under investigation.

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