首页> 外文期刊>Journal of dairy science >Abundance and Phosphorylation State of Translation Initiation Factors in Mammary Glands of Lactating and Nonlactating Dairy Cows
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Abundance and Phosphorylation State of Translation Initiation Factors in Mammary Glands of Lactating and Nonlactating Dairy Cows

机译:泌乳和非泌乳奶牛乳腺中翻译起始因子的丰度和磷酸化状态

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To test if control of mRNA translation is involved in the increase in protein synthesis by mammary glands during lactation, cellular contents and phosphorylation states of translation factors and their upstream regulators were measured in mammary parenchyma from 12 nonpregnant dairy cows. For a 42-d period, 6 cows in late lactation continued to be milked (L) and 6 at the same stage of lactation were dried off (NL). All cows were then slaughtered and mammary glands and tissue samples obtained. Alveoli and lobules tended to be larger in L cows. Mammary parenchymal mass, cell number, cell size, and RNA, DNA, and protein contents were greater in L cows. Increases (3.1- and 1.8-fold) in the abundance of active, phosphorylated ribosomal protein S6 and its kinase, S6K1, respectively, in L vs. NL parenchyma indicated an ability to sustain greater rates of synthesis of translational machinery, which was also evident in the 102% increase in parenchymal RNA:DNA between the 2 groups. Cellular abundances of the main eukaryotic translation initiation factors (eIF), eIF2 and eIF4E, were 2.6- and 3-fold greater, respectively, in L cows. That these differences were greater than the 102% greater RNA:DNA in L mammary parenchyma suggests an elevated translational efficiency in L glands. Abundance of phosphorylated rpS6 was not different between mammary parenchyma and liver, whereas eIF2α was 50% greater in mammary tissue. In semimembranosus muscle, abundances of phosphorylated rpS6 and eIF2α were 3 to 4 times lower than in mammary parenchyma. In both L and NL mammary glands, 11% of eIF2α was in the inhibitory, phosphorylated form and 48 to 60% of eIF4E was complexed with its binding protein, 4EBP1. It is concluded that up-regulation of initiation of mRNA translation occurs in the fully differentiated milk secretory cell and that, where crucial initiation factors are not present in a maximally active form, the initiation rate might be flexible in response to external stimuli.
机译:为了测试泌乳过程中乳腺蛋白质合成的增加是否涉及对mRNA翻译的控制,在12头未怀孕的奶牛的乳腺实质中测量了翻译因子及其上游调节因子的细胞含量和磷酸化状态。在42天的时间内,持续泌乳的6头母牛被挤奶(L),处于泌乳相同阶段的6头母牛被烘干(NL)。然后将所有母牛屠宰,并获得乳腺和组织样本。 L型奶牛的肺泡和小叶往往较大。 L头母牛的乳腺实质质量,细胞数量,细胞大小以及RNA,DNA和蛋白质含量更高。 L对NL实质中活性磷酸化核糖体蛋白S6及其激酶S6K1的丰度分别增加(3.1倍和1.8倍),表明有能力维持更高的翻译机器合成速率,这也很明显两组之间的实质RNA:DNA增加102%。 L奶牛的主要真核翻译起始因子(eIF),eIF2和eIF4E的细胞丰度分别高2.6倍和3倍。这些差异大于L乳腺实质中的RNA:DNA的102%,表明L腺的翻译效率提高。乳腺实质和肝脏之间磷酸化rpS6的丰度没有差异,而乳腺组织中的eIF2α则高出50%。在半膜肌中,磷酸化的rpS6和eIF2α的丰度比乳腺实质中的低3至4倍。在L和NL乳腺中,11%的eIF2α处于抑制性磷酸化形式,48%至60%的eIF4E与它的结合蛋白4EBP1复合。结论是,mRNA翻译起始的上调发生在完全分化的乳汁分泌细胞中,并且在关键的起始因子不以最大活性形式存在的情况下,起始速率可能对外部刺激有弹性。

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