首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >RAT SKELETAL MUSCLE SELENOPROTEIN W - CDNA CLONE AND MRNA MODULATION BY DIETARY SELENIUM
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RAT SKELETAL MUSCLE SELENOPROTEIN W - CDNA CLONE AND MRNA MODULATION BY DIETARY SELENIUM

机译:膳食硒对大鼠骨骼肌硒蛋白W-CDNA的克隆和MRNA的调控。

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Rat skeletal muscle selenoprotein W cDNA was isolated and sequenced. The isolation strategy involved design of degenerate PCR primers from reverse translation of a partial Peptide sequence. A reverse transcription-coupled PCR product from rat muscle mRNA was used to screen a muscle cDNA library prepared from selenium-supplemented rats. The cDNA sequence confirmed the known protein primary sequence, including a selenocysteine residue encoded by TGA, and identified residues needed to complete the protein sequence. RNA folding algorithms predict a stem-loop structure in the 3' untranslated region of the selenoprotein W mRNA that resembles selenocysteine insertion sequence (SECIS) elements identified in other selenocysteine coding cDNAs. Dietary regulation of selenoprotein W mRNA was examined in rat muscle. Dietary selenium at 0.1 ppm as selenite increased muscle mRNA 4-fold relative to a selenium-deficient diet. Higher dietary selenium produced no further increase in mRNA levels. [References: 41]
机译:分离并测序大鼠骨骼肌硒蛋白W cDNA。分离策略涉及根据部分肽序列的反向翻译设计简并PCR引物。来自大鼠肌肉mRNA的逆转录偶联PCR产物用于筛选由硒补充的大鼠制备的肌肉cDNA文库。 cDNA序列确认了已知的蛋白质一级序列,包括由TGA编码的硒代半胱氨酸残基,并鉴定了完成该蛋白质序列所需的残基。 RNA折叠算法可预测硒蛋白W mRNA 3'非翻译区的茎环结构,类似于在其他硒代半胱氨酸编码cDNA中鉴定出的硒代半胱氨酸插入序列(SECIS)元件。在大鼠肌肉中检查了硒蛋白W mRNA的饮食调节。相对于缺乏硒的饮食,以硒含量为0.1 ppm的饮食硒可使肌肉mRNA含量增加4倍。饮食中的硒含量较高时,mRNA水平不再增加。 [参考:41]

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