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首页> 外文期刊>Aquaculture >Isolation of cDNA, genomic organization and expression of small androgen receptor-interacting protein 1 (PmSARIP1) in the giant tiger shrimp Penaeus monodon.
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Isolation of cDNA, genomic organization and expression of small androgen receptor-interacting protein 1 (PmSARIP1) in the giant tiger shrimp Penaeus monodon.

机译:老虎对虾斑节对虾的cDNA分离,基因组组织和小雄激素受体相互作用蛋白1(PmSARIP1)的表达。

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摘要

The full-length cDNA and genomic organization of small androgen receptor-interacting protein 1 (SARIP1; also called RWD-containing protein 1, Rwdd1) in the giant tiger shrimp (Penaeus monodon) was isolated and characterized. PmSARIP1 was 1366 bp in length containing an open reading frame (ORF) of 738 bp corresponding to a polypeptide of 245 amino acids. Its genomic sequence contained 5 exons, 4 introns and untranslated regions (UTRs) spanning 5937 bp in length. Tissue distribution analysis indicated that PmSARIP1 was specifically expressed in gonads (ovaries > testes) but not in other tissues of wild P. monodon adults. The expression level of PmSARIP1 was not differentially expressed during ovarian maturation in intact wild adults (P>0.05). Eyestalk ablation resulted in up-regulation of PmSARIP1 throughout the ovarian maturation of wild adults where the peak level was observed at stage I (previtellogenic) ovaries (P<0.05). PmSARIP1 mRNA was clearly localized in ooplasm of previtellogenic oocytes. Serotonin injection (5-HT, 50 micro g/g body weight; 18-month-old shrimp) promoted the expression level of ovarian PmSARIP1 at 6-72 h post injection (hpi) with the peak level at 12 hpi (P<0.05). Exogenous progesterone administration (0.1 micro g/g BW; 14-month-old shrimp) did not significantly affect the expression level of ovarian PmSARIP1. In contrast, 17 beta -estradiol treatment (0.01 micro g/g BW) resulted in an increase of PmSARIP1 in 14-month-old shrimp at 7 days post injection (dpi). Results from this study suggested that PmSARIP1 should play an important role during ovarian maturation of P. monodon.
机译:分离并鉴定了大型老虎虾(斑节对虾)中与雄激素受体相互作用的小蛋白1(SARIP1;也称为含RWD的蛋白1,Rwdd1)的全长cDNA和基因组结构。 PmSARIP1的长度为1366 bp,包含738 bp的开放阅读框(ORF),对应于245个氨基酸的多肽。它的基因组序列包含5个外显子,4个内含子和长度为5937 bp的非翻译区(UTR)。组织分布分析表明,PmSARIP1在性腺(卵巢>睾丸)中特异性表达,但在野生斑节对虾成年动物的其他组织中没有特异性表达。在完整的野生成年人卵巢成熟过程中,PmSARIP1的表达水平没有差异性表达(P> 0.05)。眼球消融导致野生成人卵巢成熟过程中PmSARIP1上调,其中在I期(成胎前)卵巢观察到峰值水平(P <0.05)。 PmSARIP1 mRNA明显位于卵原性卵母细胞的卵质中。血清素注射(5-HT,50微克/克体重; 18个月大的对虾)在注射后(hpi)6-72 h促进卵巢PmSARIP1表达水平,峰值水平在12 hpi(P <0.05) )。外源孕激素给药(0.1微克/克体重; 14个月大的对虾)对卵巢PmSARIP1的表达水平没有显着影响。相反,在注射后7天(dpi),17β-雌二醇处理(0.01 micro g / g BW)导致14个月大虾中PmSARIP1的增加。这项研究的结果表明,PmSARIP1在斑节对虾的卵巢成熟过程中应发挥重要作用。

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