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首页> 外文期刊>Fish Physiology and Biochemistry >Cloning and spatiotemporal expression of pepsinogen and gastric proton pump genes from mandarin fish (Siniperca chuatsi) during early ontogeny
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Cloning and spatiotemporal expression of pepsinogen and gastric proton pump genes from mandarin fish (Siniperca chuatsi) during early ontogeny

机译:onto鱼S体发育初期胃蛋白酶原和胃质子泵基因的克隆及时空表达

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A fully developed stomach, characterized by the secretion of pepsinogens and chlorhydric acid, is vital for digestion and survival of fish larvae. To further understand the functional development of the stomach of mandarin fish (Siniperca chuatsi) during early ontogeny, the temporal and spatial expression of pepsinogens (PG A1, A2 and C), as well as proton pump genes were analyzed in the stomach from 0 to 40 days post-hatch (dph) by reverse transcription polymerase chain reaction (RT-PCR) and in situ hybridization (ISH) techniques. Pepsinogen C cDNA was firstly cloned with a full length of 1,557 bp, which contained a 37-bp 5'-untranslated region (UTR), an open reading frame of 1,164 bp encoding a polypeptide of 387 amino acids (aa) residues and a 356-bp 3'-UTR. RT-PCR analysis revealed a sequential expression mode of three pepsinogens (PG A1, A2 and C) along the ontogeny of the stomach in mandarin fish. Pepsinogen A1 was firstly detected at 4 dph (84 degree-days, dd) ahead of the appearance of gastric glands; pepsinogen A2 appeared at 12 dph (252 dd) and became the predominant form in the stomach after 19 dph (399 dd); pepsinogen C was the latest expressed gene at 14 dph (294 dd). Expression of proton pump at 12 dph (252 dd), coinciding with the expression time of pepsinogen A2 showed an excellent coordinated transcription mode between proton pump and pepsinogens. ISH analysis located the expression of three pepsinogens and alpha subunit of proton pump in the same gastric gland cells, which confirmed that they belonged to oxynticopeptic cells. In addition, oxynticopeptic cells developed and increased gradually from 14 to 40 dph. No transcripts of pepsinogens or proton pump were detected in surface mucous cells and mucous neck cells of the gastric mucosa. Our results implied the functional development of stomach in mandarin fish was closely related to pepsinogens expression.
机译:胃的充分发育以胃蛋白酶原和盐酸的分泌为特征,对鱼幼虫的消化和存活至关重要。为了进一步了解of鱼在早期个体发育过程中胃的功能发育,分析了胃中胃蛋白酶原(PG A1,A2和C)的时间和空间表达以及质子泵基因从0到0的表达。孵化后40天(dph),采用逆转录聚合酶链反应(RT-PCR)和原位杂交(ISH)技术。首先克隆胃蛋白酶原C cDNA,全长1,557 bp,包含一个37 bp的5'-非翻译区(UTR),一个1,164 bp的开放阅读框,编码387个氨基酸(aa)残基的多肽和一个356 -bp 3'-UTR。 RT-PCR分析显示man鱼中胃的三种胃蛋白酶原(PG A1,A2和C)的顺序表达模式。首先在胃腺出现之前4 dph(84度日,dd)检测到胃蛋白酶原A1。胃蛋白酶原A2在12 dph(252 dd)时出现,并在19 dph(399 dd)后成为胃中的主要形式。胃蛋白酶原C是14 dph(294 dd)时最新表达的基因。质子泵在12 dph(252 ddph)时的表达与胃蛋白酶原A2的表达时间相吻合,表明质子泵和胃蛋白酶原之间具有极好的协调转录模式。 ISH分析在相同的胃腺细胞中定位了三种胃蛋白酶原和质子泵的α亚单位的表达,证实它们属于催产光感受器细胞。此外,催产光敏细胞发育并从14 dph逐渐增加到40 dph。在胃粘膜的表面粘液细胞和粘液颈细胞中未检测到胃蛋白酶原或质子泵的转录本。我们的结果表明man鱼的胃功能发育与胃蛋白酶原表达密切相关。

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