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一种用于筛选细胞系、血液和肿瘤的简单p53功能检测方法。

A simple p53 functional assay for screening cell lines, blood, and tumors.

作者信息

Flaman J M, Frebourg T, Moreau V, Charbonnier F, Martin C, Chappuis P, Sappino A P, Limacher I M, Bron L, Benhattar J

机构信息

Unité de Génétique Moléculaire, Centre Hospitalier, Universitaire de Rouen, France.

出版信息

Proc Natl Acad Sci U S A. 1995 Apr 25;92(9):3963-7. doi: 10.1073/pnas.92.9.3963.

DOI:10.1073/pnas.92.9.3963
PMID:7732013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC42082/
Abstract

Mutations in the p53 gene are implicated in the pathogenesis of half of all human tumors. We have developed a simple functional assay for p53 mutation in which human p53 expressed in Saccharomyces cerevisiae activates transcription of the ADE2 gene. Consequently, yeast colonies containing wild-type p53 are white and colonies containing mutant p53 are red. Since this assay tests the critical biological function of p53, it can distinguish inactivating mutations from functionally silent mutations. By combining this approach with gap repair techniques in which unpurified p53 reverse transcription-PCR products are cloned by homologous recombination in vivo it is possible to screen large numbers of samples and multiple clones per sample for biologically important mutations. This means that mutations can be detected in tumor specimens contaminated with large amounts of normal tissue. In addition, the assay detects temperature-sensitive mutants, which give pink colonies. We show here that this form of p53 functional assay can be used rapidly to detect germline mutations in blood samples, somatic mutations in tumors, and mutations in cell lines.

摘要

p53基因的突变与一半的人类肿瘤发病机制有关。我们开发了一种简单的p53突变功能检测方法,其中在酿酒酵母中表达的人p53激活ADE2基因的转录。因此,含有野生型p53的酵母菌落是白色的,而含有突变型p53的菌落是红色的。由于该检测方法测试了p53的关键生物学功能,它可以区分失活突变和功能沉默突变。通过将这种方法与缺口修复技术相结合,在缺口修复技术中,未纯化的p53逆转录-PCR产物通过体内同源重组进行克隆,就有可能对大量样本和每个样本的多个克隆进行生物学重要突变的筛选。这意味着可以在被大量正常组织污染的肿瘤标本中检测到突变。此外,该检测方法还能检测出产生粉红色菌落的温度敏感突变体。我们在此表明,这种形式的p53功能检测方法可快速用于检测血液样本中的种系突变、肿瘤中的体细胞突变以及细胞系中的突变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4d0/42082/cf672f6a2cfb/pnas01493-0342-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4d0/42082/757db2c4764b/pnas01493-0340-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4d0/42082/c297cc98724d/pnas01493-0341-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4d0/42082/4843fe9c0583/pnas01493-0341-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4d0/42082/cf672f6a2cfb/pnas01493-0342-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4d0/42082/757db2c4764b/pnas01493-0340-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4d0/42082/c297cc98724d/pnas01493-0341-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4d0/42082/4843fe9c0583/pnas01493-0341-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4d0/42082/cf672f6a2cfb/pnas01493-0342-a.jpg

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