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首页> 外文期刊>General and comparative endocrinology >Molecular characterization, mRNA expression of prolactin receptor (PRLR) gene during pregnancy, nonpregnancy in the yak (Bos grunniens)
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Molecular characterization, mRNA expression of prolactin receptor (PRLR) gene during pregnancy, nonpregnancy in the yak (Bos grunniens)

机译:pregnancy牛(Bos grunniens)的分子特征,催乳素受体(PRLR)基因的mRNA表达在怀孕期间,未怀孕

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Prolactin (PRL) plays central roles in a wide range of body functions in mammals, and the actions are mediated by the specific cell surface receptor, the prolactin receptor (PRLR). To better understand the role of PRL in the yak (Bos grunniens), in the present study, we first cloned yak PRLR cDNA, and compared its mRNA expression in several tissues with cattle (Bos taurus). By reverse transcriptase-polymerase chain reaction (RT-PCR) strategy, we obtained full-length of yak PRLR cDNA sequence comprised of an open reading frame of 1746. bp encoding a 581 amino acid protein, and contained a signal sequence and a transmembrane region. The intracellular domain had two pairs of cysteine residues and a WSXWS motif. The cytoplasmic domain comprised 323 residues and contained box 1 sequence. The yak PRLR shared 66.0-98.5% protein sequence identity with mammalian homologs. Real-time PCR analysis revealed that PRLR mRNA was higher in mammary tissue than in ovary and endometrium (P<0.01). During pregnancy, the ovary and mammary PRLR mRNA expression increased by 33- and 2.9-fold in yak, respectively, and increased by 46- and 3.8-fold in cattle, respectively. PRLR mRNA expression was higher (P<0.05) in mammary tissue and ovary of pregnant cow than that of pregnant yak. It is proposed that the increased ovarian and mammary PRLR mRNA expression during pregnancy may be associated with corpus luteum function for maintenance of pregnancy and mammary development for subsequent lactation.
机译:催乳素(PRL)在哺乳动物的各种身体机能中起着核心作用,其作用由特定的细胞表面受体催乳素受体(PRLR)介导。为了更好地了解PRL在the牛(Bos grunniens)中的作用,在本研究中,我们首先克隆了ak牛PRLR cDNA,并比较了其与牛(Bos taurus)在一些组织中的mRNA表达。通过逆转录聚合酶链反应(RT-PCR)策略,我们获得了full牛PRLR cDNA的全长序列,该序列由1746个开放阅读框组成。bp编码581个氨基酸,并包含信号序列和跨膜区。细胞内结构域具有两对半胱氨酸残基和一个WSXWS基序。胞质结构域包含323个残基并且包含框1序列。牛PRLR与哺乳动物同系物共享66.0-98.5%的蛋白质序列同一性。实时PCR分析显示,乳腺组织中PRLR mRNA高于卵巢和子宫内膜(P <0.01)。在怀孕期间,牛的卵巢和乳腺PRLR mRNA表达分别增加33倍和2.9倍,而牛分别增加46倍和3.8倍。 LR牛的乳腺组织和卵巢中PRLR mRNA的表达较高(P <0.05)。有人提出,妊娠期间卵巢和乳腺PRLR mRNA表达的增加可能与黄体功能维持妊娠和乳腺发育有关(随后哺乳)有关。

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