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热休克蛋白27基因:聚肌苷酸-聚胞苷酸(Poly (I:C))诱导后的克隆、表达及与其他热休克蛋白基因的比较

Heat Shock Protein 27 Gene: Cloning, Expression, and Comparison with Other Heat Shock Protein Genes after Poly (I:C) Induction.

作者信息

Zhang Jianlu, Zhang Kunyang, Huang Jiqin, Jiang Wei, Ma Hongying, Deng Jie, Zhang Hongxing, Li Wanchun, Wang Qijun

机构信息

Shaanxi Key Laboratory of Qinling Ecological Security, Shaanxi Institute of Zoology, Xi'an 710032, China.

Key Laboratory for Hydrobiology in Liaoning Province, College of Fisheries and Life Science, Dalian Ocean University, Dalian 116023, China.

出版信息

Animals (Basel). 2022 Aug 10;12(16):2034. doi: 10.3390/ani12162034.

Abstract

We identified and cloned cDNA encoding the heat shock protein (Hsp) 27 gene from Schizothorax prenanti (SpHsp27), and compared its expression with that of SpHsp60, SpHsp70, and SpHsp90 in the liver, head kidney, hindgut, and spleen of S. prenanti that were injected with polyinosinic-polycytidylic acid [Poly (I:C)]. The SpHsp27 partial cDNA (sequence length, 653 bp; estimated molecular mass, 5.31 kDa; theoretical isoelectric point, 5.09) contained an open reading frame of 636 bp and a gene encoding 211 amino acids. The SpHsp27 amino acid sequence shared 61.0−92.89% identity with Hsp27 sequences from other vertebrates and SpHsp27 was expressed in seven S. prenanti tissues. Poly (I:C) significantly upregulated most SpHsps genes in the tissues at 12 or 24 h (p < 0.05) compared with control fish that were injected with phosphate-buffered saline. However, the intensity of responses of the four SpHsps was organ-specifically increased. The expression of SpHsp27 was increased 163-fold in the head kidney and 26.6-fold SpHsp27 in the liver at 24 h after Poly (I:C) injection. In contrast, SpHsp60 was increased 0.97−1.46-fold in four tissues and SpHsp90 was increased 1.21- and 1.16-fold in the liver and spleen at 12 h after Poly (I:C) injection. Our findings indicated that Poly (I:C) induced SpHsp27, SpHsp60, SpHsp70, and SpHsp90 expression and these organ-specific SpHsps are potentially involved in S. prenanti antiviral immunity or mediate pathological process.

摘要

我们从齐口裂腹鱼(Schizothorax prenanti,SpHsp27)中鉴定并克隆了编码热休克蛋白(Hsp)27基因的cDNA,并比较了其与注射聚肌苷酸-聚胞苷酸[Poly(I:C)]的齐口裂腹鱼肝脏、头肾、后肠和脾脏中SpHsp60、SpHsp70和SpHsp90的表达情况。SpHsp27部分cDNA(序列长度653 bp;估计分子量5.31 kDa;理论等电点5.09)包含一个636 bp的开放阅读框和一个编码211个氨基酸的基因。SpHsp27氨基酸序列与其他脊椎动物的Hsp27序列具有61.0−92.89%的同一性,且SpHsp27在齐口裂腹鱼的7个组织中表达。与注射磷酸盐缓冲盐水的对照鱼相比,Poly(I:C)在12或24小时时显著上调了大多数组织中SpHsps基因的表达(p < 0.05)。然而,四种SpHsps的反应强度在器官特异性上有所增加。Poly(I:C)注射后24小时,头肾中SpHsp27的表达增加了163倍,肝脏中SpHsp27的表达增加了26.6倍。相比之下,Poly(I:C)注射后12小时,四个组织中SpHsp60增加了0.97−1.46倍,肝脏和脾脏中SpHsp90分别增加了1.21倍和1.16倍。我们的研究结果表明,Poly(I:C)诱导了SpHsp27、SpHsp60、SpHsp70和SpHsp90的表达,这些器官特异性的SpHsps可能参与齐口裂腹鱼的抗病毒免疫或介导病理过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ff8/9404436/19e704191a2a/animals-12-02034-g001.jpg

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