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生长与分化过程中核c-ets-1蛋白与c-myb基因内含子I片段的差异性结合

Differential binding of nuclear c-ets-1 protein to an intron I fragment of the c-myb gene in growth versus differentiation.

作者信息

Wang L G, Liu X M, Li Z R, Denstman S, Bloch A

机构信息

Roswell Park Cancer Institute, Grace Cancer Drug Center, Buffalo, New York 14263.

出版信息

Cell Growth Differ. 1994 Nov;5(11):1243-51.

PMID:7848925
Abstract

For growth, ML-1 human myeloblastic leukemia cells require insulin-like growth factor 1 together with transferrin, whereas for differentiation they depend upon transforming growth factor beta in combination with transferrin. As shown in this study, growth stimulation is accompanied by c-myb expression, whereas initiation of differentiation results in the cessation of c-myb expression through premature termination of transcription in the first intron of the myb gene. Growth factor-stimulated c-myb elongation was found to correlate with an elevated level of nuclear c-ets-1 protein and with increased binding of this protein to an 18-base pair sequence in intron 1 of the c-myb gene containing the putative regulatory element PEA 3. In contrast, differentiation factor-initiated ML-1 cell maturation was accompanied by a very low level of nuclear c-ets-1 protein, by the inability to detect binding of the protein to the 18-base pair sequence, and by the cessation of c-myb expression. These results show a correlation to exist between c-ets-1 binding to intron 1 of the c-myb gene and c-myb expression. The mechanism underlying this correlation is under further study.

摘要

对于ML-1人髓母细胞白血病细胞的生长而言,需要胰岛素样生长因子1与转铁蛋白共同作用;而对于其分化来说,则依赖于转化生长因子β与转铁蛋白的联合作用。如本研究所示,生长刺激伴随着c-myb的表达,而分化的启动则通过myb基因第一内含子转录的提前终止导致c-myb表达的停止。发现生长因子刺激的c-myb延伸与核c-ets-1蛋白水平的升高以及该蛋白与c-myb基因内含子1中包含假定调控元件PEA 3的18碱基对序列结合的增加相关。相反,分化因子启动的ML-1细胞成熟伴随着极低水平的核c-ets-1蛋白,无法检测到该蛋白与18碱基对序列的结合,以及c-myb表达的停止。这些结果表明c-ets-1与c-myb基因内含子1的结合和c-myb表达之间存在相关性。这种相关性背后的机制正在进一步研究中。

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