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人类ets-1蛋白的异构体:通过可变剪接和差异磷酸化产生

Isoforms of the human ets-1 protein: generation by alternative splicing and differential phosphorylation.

作者信息

Koizumi S, Fisher R J, Fujiwara S, Jorcyk C, Bhat N K, Seth A, Papas T S

机构信息

Laboratory of Molecular Oncology, National Cancer Institute, Frederick, Maryland.

出版信息

Oncogene. 1990 May;5(5):675-81.

PMID:2189104
Abstract

The ets-1 gene belongs to the ets gene family (ets-1, ets-2, erg, and elk) and is homologous to the v-ets oncogene found in the avian leukemia virus E26. The ets-1 gene products were characterized using a specific monoclonal antibody developed against a bacterially expressed v-ets protein. The ets-1 gene product in the human T-cell line CEM was found to consist of at least six species: four major species with apparent molecular weights of 51 kDa (p51), 48 kDa (p48), 42 kDa (p42), and 39 kDa (p39); and two minor species of 52 kDa (pp52) and 49 kDa (pp49), which are demonstrated to be the phosphorylated forms of p51 and p48, respectively. All of the ets-1 proteins are related to each other and are considered products of the ets-1 gene. Subcellular localization showed that the pp52 and p51 are found mainly in the cytoplasm, while p48 and p39 are found mainly in the nucleus. Specific antibodies against various exons of ets-1 showed that both p42 and p39 lack a region corresponding to exon VII. Polymerase chain reaction analyses revealed the presence of an additional RNA product that corresponds to mRNA lacking exon VII. These results suggest that the human ets-1 gene encodes multiple proteins that are generated by at least two distinct mechanisms: alternative splicing of mRNA and protein phosphorylation.

摘要

ets-1基因属于ets基因家族(ets-1、ets-2、erg和elk),与在禽白血病病毒E26中发现的v-ets癌基因同源。使用针对细菌表达的v-ets蛋白开发的特异性单克隆抗体对ets-1基因产物进行了表征。发现人T细胞系CEM中的ets-1基因产物至少由六种组成:四种主要产物,表观分子量分别为51 kDa(p51)、48 kDa(p48)、42 kDa(p42)和39 kDa(p39);以及两种次要产物,52 kDa(pp52)和49 kDa(pp49),分别被证明是p51和p48的磷酸化形式。所有ets-1蛋白相互关联,被认为是ets-1基因的产物。亚细胞定位显示,pp52和p51主要存在于细胞质中,而p48和p39主要存在于细胞核中。针对ets-1各个外显子的特异性抗体表明,p42和p39都缺少对应于外显子VII的区域。聚合酶链反应分析揭示了存在一种额外的RNA产物,其对应于缺少外显子VII的mRNA。这些结果表明,人类ets-1基因编码多种蛋白质,这些蛋白质通过至少两种不同机制产生:mRNA的可变剪接和蛋白质磷酸化。

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