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在F9胚胎癌细胞分化过程中,一种91千道尔顿的PEA3结合蛋白的表达下调。

Expression of a 91-kilodalton PEA3-binding protein is down-regulated during differentiation of F9 embryonal carcinoma cells.

作者信息

Martin M E, Yang X Y, Folk W R

机构信息

Department of Biochemistry, University of Missouri, Columbia 65212.

出版信息

Mol Cell Biol. 1992 May;12(5):2213-21. doi: 10.1128/mcb.12.5.2213-2221.1992.

Abstract

Proteins binding to the PEA3 enhancer motif (AGGAAG) activate the polyomavirus early promoter and help comprise the viral late mRNA initiator element (W. Yoo, M. E. Martin, and W. R. Folk, J. Virol. 65:5391-5400, 1991). Because many developmentally regulated cellular genes have PEA3 motifs near their promoter sequences, and because Ets family gene products activate the PEA3 motif, we have studied the expression of PEA3-binding proteins and Ets-related proteins during differentiation of F9 embryonal carcinoma cells. An approximately 91-kDa protein (PEA3-91) was identified in F9 cell nuclear extracts by UV cross-linking to a radiolabeled PEA3 oligonucleotide probe, and expression of PEA3-91 was down-regulated after differentiation of F9 cells to parietal endoderm. The c-ets-1 gene product binds to a sequence in the murine sarcoma virus long terminal repeat that is similar to the PEA3 motif (cGGAAG), but PEA3-91 was not cross-linked to this Ets-1-binding motif, nor did antiserum which recognizes murine c-ets-1 and c-ets-2 proteins have any effect on PEA3-binding activity in mobility shift assays. Furthermore, c-ets-1 mRNA was not detected in undifferentiated or differentiated F9 cells, and c-ets-2 mRNA levels remained high after differentiation. Antiserum against the Drosophila Ets-related E74A protein, however, recognized an approximately 92-kDa protein in F9 cells whose expression during differentiation varied in a manner identical to that of PEA3-91. These data suggest that PEA3-91 is not the product of the ets-1 or ets-2 genes but is likely to be the product of a murine homolog of the Drosophila E74 gene.

摘要

与PEA3增强子基序(AGGAAG)结合的蛋白质可激活多瘤病毒早期启动子,并有助于构成病毒晚期mRNA起始元件(W. Yoo、M. E. Martin和W. R. Folk,《病毒学杂志》65:5391 - 5400,1991年)。由于许多发育调控的细胞基因在其启动子序列附近具有PEA3基序,并且由于Ets家族基因产物可激活PEA3基序,我们研究了F9胚胎癌细胞分化过程中PEA3结合蛋白和Ets相关蛋白的表达情况。通过与放射性标记的PEA3寡核苷酸探针进行紫外线交联,在F9细胞核提取物中鉴定出一种约91 kDa的蛋白质(PEA3 - 91),F9细胞分化为壁内胚层后,PEA3 - 91的表达下调。c - ets - 1基因产物与鼠肉瘤病毒长末端重复序列中一个类似于PEA3基序(cGGAAG)的序列结合,但PEA3 - 91未与该Ets - 1结合基序交联,在迁移率变动分析中,识别鼠c - ets - 1和c - ets - 2蛋白的抗血清对PEA3结合活性也没有任何影响。此外,在未分化或分化的F9细胞中均未检测到c - ets - 1 mRNA,分化后c - ets - 2 mRNA水平仍保持较高。然而,针对果蝇Ets相关的E74A蛋白的抗血清识别出F9细胞中一种约92 kDa的蛋白质,其在分化过程中的表达变化方式与PEA3 - 91相同。这些数据表明,PEA3 - 91不是ets - 1或ets - 2基因的产物,而可能是果蝇E74基因鼠同源物的产物。

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