首页> 外文期刊>Cell biochemistry and function >Identification of heterogeneous nuclear ribonucleoprotein A/B as a cytoplasmic mRNA-binding protein in early involution of the mouse mammary gland.
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Identification of heterogeneous nuclear ribonucleoprotein A/B as a cytoplasmic mRNA-binding protein in early involution of the mouse mammary gland.

机译:小鼠乳腺早期复性中异质核核糖核蛋白A / B的鉴定为胞质mRNA结合蛋白。

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摘要

Involution of the mammary gland is a regressive phase that occurs after lactation, and requires reprogramming of gene expression for the tissue to return to a pre-pregnant state. Although the transcriptome of the mammary gland demonstrates complex changes at the mRNA level, the molecular mechanisms governing post-transcriptional control remain obscure. In the present study, we isolated cytoplasmic mRNA-protein complexes (mRNPs) from the mouse mammary gland at the early involution stage using discontinuous sucrose density ultracentrifugation. mRNPs including untranslated mRNAs were then purified with oligo(dT) immobilized on cellulose or paramagnetic beads. Proteins in the purified complexes were subjected to one/two-dimensional gel electrophoresis followed by mass spectrometry. This identified heterogeneous nuclear ribonucleoprotein A/B (Hnrpab), along with three other heterogeneous nuclear ribonucleoproteins. Hnrpab in the mRNPs reproducibly increased within 48 h after weaning and became one of the major components. When a vector expressing Hnrpab was transfected into two different cell lines, their growth was suppressed, demonstrating that this protein has cytostatic activity. These results suggest that early involution can be used as a model for understanding the mechanism of post-transcriptional control of gene expression, responsible for modulation of cell function.
机译:乳腺的退化是泌乳后发生的一种退行期,需要对基因表达进行重新编程,以使组织恢复到怀孕前的状态。尽管乳腺的转录组在mRNA水平显示出复杂的变化,但是控制转录后控制的分子机制仍然不清楚。在本研究中,我们使用不连续的蔗糖密度超速离心从内卷初期的小鼠乳腺中分离出细胞质mRNA-蛋白质复合物(mRNPs)。然后用固定在纤维素或顺磁珠上的oligo(dT)纯化包括未翻译的mRNA在内的mRNP。对纯化的复合物中的蛋白质进行一维/二维凝胶电泳,然后进行质谱分析。这确定了异质核糖核蛋白A / B(Hnrpab),以及其他三种异质核糖核蛋白。断奶后48小时内,mRNPs中的Hnrpab可再现地增加,并成为主要成分之一。当将表达Hnrpab的载体转染到两个不同的细胞系中时,它们的生长被抑制,表明该蛋白具有抑制细胞生长的活性。这些结果表明,早期对合可以用作理解基因表达的转录后控制机制的模型,该机制负责调节细胞功能。

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