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P63 调节 WDFY2 基因的表达,该基因与癌症调控和肢体发育有关。

P63 modulates the expression of the WDFY2 gene which is implicated in cancer regulation and limb development.

机构信息

Mutagenesis and Cancer Prevention Unit, IRCCS Ospedale Policlinico San Martino, Largo R. Benzi, 10, Genoa 16132, Italy.

Department of Cellular, Computational and Integrative Biology (CIBio), University of Trento, Via Sommarive 9, Povo (TN) 38123, Italy.

出版信息

Biosci Rep. 2019 Dec 20;39(12). doi: 10.1042/BSR20192114.

Abstract

TP63 is a member of the TP53 gene family, sharing a common gene structure that produces two groups of mRNAs' encoding proteins with different N-terminal regions (ΔN and TA isoforms); both transcripts are also subjected to alternative splicing mechanisms at C-terminus, generating a variety of isoforms. p63 is a master regulator of epidermal development and homoeostasis as well as an important player in tumorigenesis and cancer progression with both oncogenic and tumour suppressive roles. A number of studies have aimed at the identification of p63 target genes, allowing the dissection of the molecular pathways orchestrated by the different isoforms. In the present study we investigated in more detail the p63 responsiveness of the WDFY2 (WD repeat and FYVE domain containing 2) gene, encoding for an endosomal protein identified as a binding partner of the PI-3K/AKT signalling pathway. We showed that overexpression of different p63 isoforms was able to induce WDFY2 expression in TP53-null cells. The p63-dependent transcriptional activation was associated with specific response elements (REs) that have been identified by a bioinformatics tool and validated by yeast- and mammal-based assays. Interestingly, to confirm that WDFY2 belongs to the p63 network of cancer regulation, we analysed the impact of WDFY2 alterations, by showing its frequent deletion in different types of tumours and suggesting its expression level as a prognostic biomarker. Lastly, we identified a chromosomal translocation involving the WDFY2 locus in a patient affected by a rare congenital limb anomaly, indicating WDFY2 as a possible susceptibility gene placed downstream p63 in the network of limb development.

摘要

TP63 是 TP53 基因家族的成员,具有共同的基因结构,产生两组编码具有不同 N 端区域(ΔN 和 TA 异构体)的蛋白质的 mRNAs;这两种转录本在 C 端也受到选择性剪接机制的影响,产生多种异构体。p63 是表皮发育和同源性的主要调节因子,也是肿瘤发生和癌症进展中的重要参与者,具有致癌和肿瘤抑制作用。许多研究旨在鉴定 p63 的靶基因,从而剖析不同异构体协调的分子途径。在本研究中,我们更详细地研究了 WDFY2(WD 重复和 FYVE 结构域包含 2)基因的 p63 反应性,该基因编码一种内体蛋白,被鉴定为 PI-3K/AKT 信号通路的结合伴侣。我们表明,不同 p63 异构体的过表达能够诱导 TP53 缺失细胞中 WDFY2 的表达。p63 依赖性转录激活与已通过生物信息学工具鉴定并通过酵母和哺乳动物测定验证的特定反应元件(RE)相关。有趣的是,为了证实 WDFY2 属于癌症调控的 p63 网络,我们通过显示其在不同类型肿瘤中的频繁缺失来分析 WDFY2 改变的影响,并提出其表达水平作为预后生物标志物。最后,我们在一位患有罕见先天性肢体异常的患者中鉴定出涉及 WDFY2 基因座的染色体易位,表明 WDFY2 可能是位于 p63 下游的肢体发育网络中的易感基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93e9/6914664/db80e05f3a97/bsr-39-bsr20192114-g1.jpg

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