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首页> 外文期刊>Progress in Natural Science: Communication of State Key Laboratories of China >Molecular cloning of growth hormone receptor (GHR) from common carp (Cyprinus carpio L.) and identification of its two forms of mRNA transcripts
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Molecular cloning of growth hormone receptor (GHR) from common carp (Cyprinus carpio L.) and identification of its two forms of mRNA transcripts

机译:鲤鱼(Cyprinus carpio L.)生长激素受体(GHR)的分子克隆及其两种形式的mRNA转录本的鉴定

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摘要

The cDNA of growth hormone receptor (GHR) was cloned from the liver of 2-year common carp ( Cyprinus carpio L. ) by reverse transcription-polymerase chain reaction (RT-PCR) and rapid amplification of cDNA end (RACE). Its open reading frame (ORF) of 1806 nucleotides is translated into a putative peptide of 602 amino acids, including an extracellular ligand-binding domain of 244 amino acids (aa), a single transmembrane domain of 24 aa and an intracellular signal-transduction domain of 334 aa. Sequence analysis indicated that common carp GHR is highly homologous to goldfish ( Carassius auratus) GHR at both gen? and protein levels. Using a pair of gene-specific primers, a GHR fragment was amplified from the cDNA of 2-year common carp, a 224 bp product was identified in liver and a 321 bp product in other tissues. The sequencing of the products and the partial genomic DNA indicated that the difference in product size was the result of a 97 bp intron that alternatively spliced. In addition, the 321 bp fragment could be amplified from all the tissues of 4-month common carp including liver, demonstrating the occurrence of the alternative splicing of this intron during the development of common carp. Moreover, a semi-quantitative RT-PCR was performed to analyze the expression level of GHR in tissues of 2-year common carp and 4-month common carp. The result revealed that in the tissues of gill, thymus and brain, the expression level of GHR in 2-year common carp was significantly lower than that of 4-month common carp.
机译:通过逆转录-聚合酶链反应(RT-PCR)和cDNA末端的快速扩增(RACE),从2年生鲤鱼(Cyprinus carpio L.)的肝脏中克隆了生长激素受体(GHR)的cDNA。它的1806个核苷酸的开放阅读框(ORF)被翻译成602个氨基酸的推定肽,包括244个氨基酸(aa)的细胞外配体结合结构域,24个氨基酸的单个跨膜结构域和细胞内信号转导结构域334个AA。序列分析表明,鲤鱼的GHR与两个基因的金鱼(Carassius auratus)GHR高度同源。和蛋白质水平。使用一对基因特异性引物,从2年生鲤鱼的cDNA中扩增出GHR片段,在肝脏中鉴定出224 bp的产物,在其他组织中鉴定出321 bp的产物。产物和部分基因组DNA的测序表明,产物大小的差异是一个97 bp内含子的结果,该内含子是可变剪接的。此外,可以从包括肝脏在内的4个月普通鲤鱼的所有组织中扩增321bp的片段,这表明在普通鲤鱼的发育过程中该内含子的选择性剪接发生了。此外,进行了半定量RT-PCR,以分析GHR在2年鲤和4个月鲤的组织中的表达水平。结果表明,在of,胸腺和脑组织中,两年生鲤鱼中GHR的表达水平明显低于四个月生鲤鱼。

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