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Identification and characterization of goose prolactin receptor

机译:鹅催乳素受体的鉴定与表征

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摘要

Prolactin receptor (PRLR) is a single transmembrane protein through which prolactin plays a wide variety of physiological roles in vertebrates. To understand its role in goose behavior, we cloned the gene of goose PRLR (gPRLR) in the Siji goose, a domestic goose with strong broodiness in China, and examined its expression level in different organs of adult geese. Our results showed that gPRLR cDNA contained 443 bp 5' untranslated region, 2,496 bp coding sequence that presumably comprises at least 14 exons, and 220 bp 3' untranslated region. The predicted goose PRLR contained 831 amino acids and exhibited identities of 87.7, 85.2, and 84.8% with chicken, pigeon, and turkey PRLR, respectively. It comprised a signal peptide of 24 amino acids at the N terminus, 2 ligand binding regions of the extracellular domain, each containing 2 pairs of cysteine residues and a pentapeptide of 5 amino acids known as WS motif (Tpr-Ser-any amino acid-Tpr-Ser), the 2 typical features highly conserved in the members of class 1 cytokine receptor superfamily. Phylogenetic analysis revealed that the goose PRLR is highly conserved during evolution. In addition, we discovered 2 other alternative splicing transcripts of gPRLR. One is generated by missing the last 95 bp of the first 330 bp of the 3,159 bp cDNA. The other is produced by an alternative transcription initiation, leading to creation of a novel first exon that is directly spliced to the third exon. Reverse transcription PCR analyses show that the gPRLR mRNA is widely expressed in the testis, seminal duct, ovary, oviduct, kidney, large intestine, and small intestine.
机译:催乳素受体(PRLR)是一种单一的跨膜蛋白,催乳素通过它在脊椎动物中起多种生理作用。为了了解其在鹅行为中的作用,我们在中国强烈嗜好的家鹅“四极鹅”中克隆了鹅PRLR(gPRLR)基因,并检查了其在成年鹅不同器官中的表达水平。我们的结果表明,gPRLR cDNA包含443 bp的5'非翻译区,2496 bp的编码序列(可能至少包含14个外显子)和220 bp的3'非翻译区。预测的鹅PRLR包含831个氨基酸,与鸡肉,鸽子和火鸡PRLR的同一性分别为87.7、85.2和84.8%。它包含一个位于N端的24个氨基酸的信号肽,2个胞外域配体结合区,每个区包含2对半胱氨酸残基和5个氨基酸的五肽(称为WS基序)(Tpr-Ser-任何氨基酸- Tpr-Ser),这是1类细胞因子受体超家族成员高度保守的2个典型特征。系统发育分析表明,鹅PRLR在进化过程中是高度保守的。此外,我们发现了gPRLR的其他2个其他剪接转录本。通过丢失3159 bp cDNA的前330 bp中的最后95 bp来生成一个。另一个由替代转录起始产生,导致产生直接剪接至第三外显子的新颖的第一外显子。逆转录PCR分析表明,gPRLR mRNA在睾丸,精管,卵巢,输卵管,肾脏,大肠和小肠中广泛表达。

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