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人类PTEN的统一命名法和氨基酸编号

A unified nomenclature and amino acid numbering for human PTEN.

作者信息

Pulido Rafael, Baker Suzanne J, Barata Joao T, Carracedo Arkaitz, Cid Victor J, Chin-Sang Ian D, Davé Vrushank, den Hertog Jeroen, Devreotes Peter, Eickholt Britta J, Eng Charis, Furnari Frank B, Georgescu Maria-Magdalena, Gericke Arne, Hopkins Benjamin, Jiang Xeujun, Lee Seung-Rock, Lösche Mathias, Malaney Prerna, Matias-Guiu Xavier, Molina María, Pandolfi Pier Paolo, Parsons Ramon, Pinton Paolo, Rivas Carmen, Rocha Rafael M, Rodríguez Manuel S, Ross Alonzo H, Serrano Manuel, Stambolic Vuk, Stiles Bangyan, Suzuki Akira, Tan Seong-Seng, Tonks Nicholas K, Trotman Lloyd C, Wolff Nicolas, Woscholski Rudiger, Wu Hong, Leslie Nicholas R

机构信息

Ikerbasque, Basque Foundation for Science, Bilbao, Spain. BioCruces Health Research Institute, Barakaldo, Spain.

Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, USA.

出版信息

Sci Signal. 2014 Jul 1;7(332):pe15. doi: 10.1126/scisignal.2005560.

Abstract

The tumor suppressor PTEN is a major brake for cell transformation, mainly due to its phosphatidylinositol 3,4,5-trisphosphate [PI(3,4,5)P3] phosphatase activity that directly counteracts the oncogenicity of phosphoinositide 3-kinase (PI3K). PTEN mutations are frequent in tumors and in the germ line of patients with tumor predisposition or with neurological or cognitive disorders, which makes the PTEN gene and protein a major focus of interest in current biomedical research. After almost two decades of intense investigation on the 403-residue-long PTEN protein, a previously uncharacterized form of PTEN has been discovered that contains 173 amino-terminal extra amino acids, as a result of an alternate translation initiation site. To facilitate research in the field and to avoid ambiguities in the naming and identification of PTEN amino acids from publications and databases, we propose here a unifying nomenclature and amino acid numbering for this longer form of PTEN.

摘要

肿瘤抑制因子PTEN是细胞转化的主要制动器,主要归因于其磷脂酰肌醇-3,4,5-三磷酸[PI(3,4,5)P3]磷酸酶活性,该活性直接对抗磷酸肌醇3-激酶(PI3K)的致癌性。PTEN突变在肿瘤以及具有肿瘤易感性或神经或认知障碍的患者的种系中很常见,这使得PTEN基因和蛋白成为当前生物医学研究的主要关注焦点。在对长达403个残基的PTEN蛋白进行了近二十年的深入研究之后,发现了一种以前未被表征的PTEN形式,由于一个替代的翻译起始位点,它含有173个氨基末端额外氨基酸。为了促进该领域的研究,并避免在出版物和数据库中对PTEN氨基酸的命名和识别产生歧义,我们在此为这种更长形式的PTEN提出统一的命名法和氨基酸编号。

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