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TP53基因的内含子缺失导致乳腺癌中6号外显子跳跃。

An intronic deletion in TP53 gene causes exon 6 skipping in breast cancer.

作者信息

Voglino G, Castello S, Silengo L, Stefanuto G, Friard O, Ferrara G, Fessia L

机构信息

Department of Clinical Pathology, Ospedale Sant' Anna, Turin, Italy.

出版信息

Eur J Cancer. 1997 Aug;33(9):1479-83. doi: 10.1016/s0959-8049(97)00136-6.

Abstract

Six hundred and thirty primary breast cancer were screened for abnormalities in exons 5, 6, 7 and 8 of the TP53 tumour suppressor gene. Analysis of the structure of the TP53 gene exons was performed with the polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) method and with direct sequencing of amplified DNA. In a breast tumour case from a postmenopausal patient, we found a deletion of 36 bp in intron 5 and no immunohistochemical staining for p53. We amplified and sequenced the cDNA region between exons 4 and 7 and showed that the deletion causes the skipping of exon 6. The resulting mRNA sequence had a frameshift that yields an inactive protein with a truncated C terminus. These results show the first example of intronic deletion causing exon skipping at the TP53 gene level.

摘要

对630例原发性乳腺癌进行了TP53肿瘤抑制基因第5、6、7和8外显子异常筛查。采用聚合酶链反应-单链构象多态性(PCR-SSCP)方法和扩增DNA直接测序法对TP53基因外显子结构进行分析。在1例绝经后患者的乳腺肿瘤病例中,我们发现第5内含子有36 bp的缺失,且p53无免疫组化染色。我们对第4和7外显子之间的cDNA区域进行扩增和测序,结果显示该缺失导致第6外显子跳跃。由此产生的mRNA序列发生移码,产生一个C末端截短的无活性蛋白。这些结果显示了第1例内含子缺失导致TP53基因水平外显子跳跃的例子。

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