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Effect of proline rich domain of an RNA-binding protein Sam68 in cell growth process, death and B cell signal transduction

机译:RNA结合蛋白Sam68富含脯氨酸的结构域在细胞生长过程,死亡和B细胞信号转导中的作用

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Background Sam68 plays an important role as a multiple functional RNA binding nuclear protein in cell cycle progress, RNA usage, signal transduction, and tyrosine phosphorylation by Src during mitosis. However, its precise impact on these essential cellular functions remains unclear. The purpose of this study is to further elucidate Sam68 functions in RNA metabolism, signal transduction regulation of cell growth and cell proliferation in DT40 cell line. Methods By using gene targeting method, we isolated a mutation form of Sam68 in DT40 cells and described its effect on cell growth process and signal transduction. Southern, Northern, and Western blot, phosphorylation and flow-cytometric analyses were performed to investigate the Sam68 functions. Results A slower growth rate (2.1 hours growth elongation) and longer S phase (1.7 hours elongation) was observed in the Sam68 mutant cells. Serum depletion resulted in increased amounts of dead cells, and expansion of S phase in mutant cells. Upon B cell cross-linking, the maximal level of tyrosine phosphorylation on BLNK was observed to be significantly lower in mutant cells. Conclusions The proline rich domain of Sam68 is involved in cell growth control by modulating the function of mRNAs in S phase or earlier and the functions as an adaptor molecule in B cell signal transduction pathways.
机译:背景Sam68在细胞周期进程,RNA使用,信号转导和有丝分裂过程中被Src酪氨酸磷酸化的过程中,作为多功能RNA结合核蛋白发挥着重要作用。但是,其对这些基本细胞功能的确切影响尚不清楚。这项研究的目的是进一步阐明DT40细胞系中Sam68在RNA代谢,信号传导调节细胞生长和细胞增殖中的功能。方法采用基因靶向方法,在DT40细胞中分离出Sam68突变型,并描述了其对细胞生长过程和信号转导的影响。进行了Southern,Northern和Western印迹,磷酸化和流式细胞仪分析以研究Sam68的功能。结果在Sam68突变细胞中观察到较慢的生长速率(2.1小时的生长伸长)和较长的S期(1.7小时的伸长)。血清耗竭导致死细胞数量增加,突变细胞中S期扩增。在B细胞交联后,突变细胞中BLNK上酪氨酸磷酸化的最大水平显着降低。结论Sam68富含脯氨酸的结构域通过调节S期或更早的mRNA的功能以及B细胞信号转导途径中的衔接子分子的功能来参与细胞生长控制。

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