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鲑鱼促性腺激素释放激素(GnRH)和鸡GnRH-II前体信使核糖核酸在金鱼脑和卵巢中的表达

Expression of salmon gonadotropin-releasing hormone (GnRH) and chicken GnRH-II precursor messenger ribonucleic acids in the brain and ovary of goldfish.

作者信息

Lin X W, Peter R E

机构信息

Department of Biological Sciences, University of Alberta, Edmonton, Canada.

出版信息

Gen Comp Endocrinol. 1996 Mar;101(3):282-96. doi: 10.1006/gcen.1996.0031.

Abstract

The complementary DNAs (cDNA) encoding the [Trp7Leu8]gonadotropin-releasing hormone (salmon GnRH; sGnRH) precursor and the [His5Trp7Tyr8]GnRH (chicken GnRH-II; cGnRH-II) precursor of the goldfish brain were isolated and sequenced using reverse transcription and rapid amplification of cDNA ends (RACE). The sGnRH precursor cDNA consists of 540 bp, including an open reading frame of 282 bp, and the cGnRH-II precursor cDNA consists of 682 bp, including an open reading frame of 258 bp. The 94 amino acid-long goldfish sGnRH precursor and 86 amino acid-long goldfish cGnRH-II precursor have the same molecular architecture as GnRH precursors identified to date in other vertebrate species. Using two sets of primers designed to be sense and antisense to the goldfish brain sGnRH precursor cDNA sequence, reverse transcription-polymerase chain reaction (RT-PCR) amplification of total RNA from brain and ovary at gonadal recrudescent, mature ( = prespawning), and postovulatory stages resulted in two predicted sizes of PCR products. The intensities of staining signals of ethidium bromide were similar between brain and ovary samples. The same RT-PCRs were carried out with two sets of primers for cGnRH-II precursor cDNA, resulting in two PCR products of predicted size; however, the ethidium bromide staining signals are much weaker for products amplified from ovarian cDNA than that from brain cDNA. Restriction enzyme analysis verified the expected RT-PCR products. Sequence analysis of ovarian sGnRH precursor cDNA generated by RACE of total RNA from recrudescent ovarian tissue revealed the identical sequence to that of the brain sGnRH cDNA. Northern blot analysis detected a single mRNA transcript of approximately 650 bases for the sGnRH precursor in both the brain and ovary, and 750 bases for the cGnRH-II precursor in the brain. These results demonstrate that two forms of GnRH precursor (sGnRH and cGnRH-II) mRNA are expressed in goldfish brain tissue and that the sGnRH transcript and a low level of cGnRH-II transcript are also expressed in the goldfish ovary.

摘要

采用逆转录和cDNA末端快速扩增(RACE)技术,分离并测序了金鱼脑内编码[色氨酸7亮氨酸8]促性腺激素释放激素(鲑鱼GnRH;sGnRH)前体和[组氨酸5色氨酸7酪氨酸8]GnRH(鸡GnRH-II;cGnRH-II)前体的互补DNA(cDNA)。sGnRH前体cDNA由540 bp组成,包括一个282 bp的开放阅读框,cGnRH-II前体cDNA由682 bp组成,包括一个258 bp的开放阅读框。94个氨基酸长的金鱼sGnRH前体和86个氨基酸长的金鱼cGnRH-II前体与迄今在其他脊椎动物物种中鉴定出的GnRH前体具有相同的分子结构。使用两组分别针对金鱼脑sGnRH前体cDNA序列设计的正义和反义引物,对性腺恢复期、成熟期(=产卵前)和排卵后阶段的脑和卵巢总RNA进行逆转录-聚合酶链反应(RT-PCR)扩增,得到了两种预测大小的PCR产物。脑和卵巢样品中溴化乙锭染色信号的强度相似。用两组针对cGnRH-II前体cDNA的引物进行相同的RT-PCR,得到了两种预测大小的PCR产物;然而,从卵巢cDNA扩增的产物的溴化乙锭染色信号比从脑cDNA扩增的产物弱得多。限制性酶切分析验证了预期的RT-PCR产物。对恢复期卵巢组织总RNA进行RACE生成的卵巢sGnRH前体cDNA的序列分析显示,其与脑sGnRH cDNA的序列相同。Northern印迹分析在脑和卵巢中均检测到一条约650个碱基的sGnRH前体单一mRNA转录本,在脑中检测到一条750个碱基的cGnRH-II前体单一mRNA转录本。这些结果表明,两种形式的GnRH前体(sGnRH和cGnRH-II)mRNA在金鱼脑组织中表达,并且sGnRH转录本和低水平的cGnRH-II转录本也在金鱼卵巢中表达。

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