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TP53的多样性概况受紧邻上游基因座WDR79上的正选择影响。

The diversity profile of TP53 is influenced by positive selection on the immediately upstream locus WDR79.

作者信息

Alonso Santos, Izagirre Neskuts, López Saioa, Smith-Zubiaga Isabel, Hervella Montse, Boyano María Dolores, Arroyo-Berdugo Yoana, Gardeazabal Jesús, Díaz-Ramón José Luís, Sánchez Díez Ana, Careaga Jesus María, de la Rúa Concepción

机构信息

Department of Genetics, Physical Anthropology and Animal Physiology, University of the Basque Country, Barrio Sarriena s/n, ES-48940 Leioa, Bizkaia, Spain.

出版信息

Hum Hered. 2010;69(1):34-44. doi: 10.1159/000243152. Epub 2009 Oct 2.

Abstract

BACKGROUND/AIM: TP53 is an efficient central node in a signal transduction network that responds to minimize cancer. However, over 50% of tumors show some mutation in TP53. Thus, one might argue that this single central node network lacks robustness. Therefore, we wanted to investigate if natural selection has played a role in shaping the genomic region containing TP53.

METHODS

We have analyzed the HapMap data for evidence of selection using F(ST) pairwise comparisons and the extended haplotype homozygosity test on a 200-kb region encompassing TP53. We have also resequenced 4 kb upstream TP53 in Europeans (including melanoma patients), Asians, Australian Aborigines and Africans.

RESULTS

Genetic hitchhiking by a linked, positively selected allele at the nearby gene WDR79 may be partly responsible for the sequence diversity profile of TP53. It can help explain why the TP53 Arg72 allele is the major allele in Europeans even when the alternative allele, 72Pro, has been reported to offer an increased longevity after disease.

CONCLUSIONS

Despite the important role of TP53, a complex interplay with other evolutionary forces, which are extrinsic to TP53 function, may have driven the genetic diversity pattern of this locus, and, as a consequence, its structure and function.

摘要

背景/目的:TP53是信号转导网络中的一个有效核心节点,该网络对癌症的发生起到最小化作用。然而,超过50%的肿瘤显示TP53存在某些突变。因此,有人可能会认为这个单一核心节点网络缺乏稳健性。所以,我们想要研究自然选择是否在塑造包含TP53的基因组区域中发挥了作用。

方法

我们使用F(ST)成对比较和扩展单倍型纯合性检验,在一个包含TP53的200 kb区域分析了HapMap数据以寻找选择的证据。我们还对欧洲人(包括黑色素瘤患者)、亚洲人、澳大利亚原住民和非洲人的TP53上游4 kb区域进行了重测序。

结果

附近基因WDR79处一个连锁的、受到正向选择的等位基因的遗传搭便车效应可能部分解释了TP53的序列多样性特征。这有助于解释为什么即使据报道替代等位基因72Pro在患病后能延长寿命,但TP53 Arg72等位基因在欧洲人中仍是主要等位基因。

结论

尽管TP53具有重要作用,但与TP53功能无关的其他进化力量之间的复杂相互作用可能驱动了该基因座的遗传多样性模式,进而影响其结构和功能。

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