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近江牡蛎Hsc70蛋白基因cDNA片段的克隆及Southern杂交和RT-PCR分析 被引量:12

Cloning,Southern blotting and RT-PCR analysis of a cDNA fragment encoding of 70 kDa heat shock cognate protein (Hsc70) from the oyster (Crassostrea ariakensis)
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摘要 In order to elucidate the molecular mechanisms of the oyster (Crassostrea ariakensis) against adverse stimulating factors, we cloned and sequenced a partial cDNA encoding a 70 kDa heat shock cognate protein (Hsc70) from the oyster. The live oysters were obtained from Chengcun, Yangxi County, Guangdong Province, China. Various tissues, including mantle, gills, adductor muscle, heart and blood cells, were respectively collected from 5 untreated live oysters or treated ones at 36℃ for 1 5 hours, and immediately frozen in liquid nitrogen except for the blood cells which were suspended with Trizol Reagent after centrifugation ( 12 000 r/min for 30 s) and stored at -20℃. Total RNA was isolated using Trizol Reagent according to the manufacture’s instructions. The first strand cDNA was synthesized using reverse transcriptase Superscript Ⅱ according to the manufacture’s instructions. The primers were designed from a conserved region of C. gigas Hsc70 cDNA sequence (GeneBank accession No. AF144646). The polymerase chain reaction (PCR) was performed for 30 cycles with denaturation at 94℃ for 30 s, annealing at 49℃ for 40 s, and elongation at 72℃ for 30 s. The product was cloned to pGEM T easy vector and sequenced. It is 509 base pairs (bp) and possesses 94% identity with the cDNA encoding C. gigas Hsc70 using Blastn. This homology was strongly confirmed by amino acid sequence comparison using the Blastx (99%). The 509 bp fragment was labeled with α 32 pdCTP and a random primer DNA labeling kit and employed as a probe to perform Southern blotting, the result demonstrated that the cDNA came from a partial mRNA transcript of C. ariakensis genomic DNA gene. The polymerase chain reaction (PCR) was carried out to investigate the expression of Hsc70, Using the cDNAs of several tissues, such as gills (heat shocked), mantle, adductor muscle (heat shocked), heart, blood cells (one sample with heat shock for 1 5 hours at 36℃ and another without any stimulus). The PCR results revealed that Hsc70 transcripts could be detected in all the tissues analyzed and greatly increased in the tissues with heat shock. The results showed that the Hsc70 is ubiquitously and constitutively expressed but can be stimulated by heat shock. All the facts above firmly established that the cloned cDNA fragment was a part of the cDNA encoding a Hsc70 protein in the oyster C. ariakensis . In order to elucidate the molecular mechanisms of the oyster (Crassostrea ariakensis) against adverse stimulating factors, we cloned and sequenced a partial cDNA encoding a 70 kDa heat shock cognate protein (Hsc70) from the oyster. The live oysters were obtained from Chengcun, Yangxi County, Guangdong Province, China. Various tissues, including mantle, gills, adductor muscle, heart and blood cells, were respectively collected from 5 untreated live oysters or treated ones at 36℃ for 1 5 hours, and immediately frozen in liquid nitrogen except for the blood cells which were suspended with Trizol Reagent after centrifugation ( 12 000 r/min for 30 s) and stored at -20℃. Total RNA was isolated using Trizol Reagent according to the manufacture's instructions. The first strand cDNA was synthesized using reverse transcriptase Superscript Ⅱ according to the manufacture's instructions. The primers were designed from a conserved region of C. gigas Hsc70 cDNA sequence (GeneBank accession No. AF144646). The polymerase chain reaction (PCR) was performed for 30 cycles with denaturation at 94℃ for 30 s, annealing at 49℃ for 40 s, and elongation at 72℃ for 30 s. The product was cloned to pGEM T easy vector and sequenced. It is 509 base pairs (bp) and possesses 94% identity with the cDNA encoding C. gigas Hsc70 using Blastn. This homology was strongly confirmed by amino acid sequence comparison using the Blastx (99%). The 509 bp fragment was labeled with α 32 pdCTP and a random primer DNA labeling kit and employed as a probe to perform Southern blotting, the result demonstrated that the cDNA came from a partial mRNA transcript of C. ariakensis genomic DNA gene. The polymerase chain reaction (PCR) was carried out to investigate the expression of Hsc70, Using the cDNAs of several tissues, such as gills (heat shocked), mantle, adductor muscle (heat shocked), heart, blood cells (one sample with heat shock for 1 5 hours at 36℃ and another without any stimulus). The PCR results revealed that Hsc70 transcripts could be detected in all the tissues analyzed and greatly increased in the tissues with heat shock. The results showed that the Hsc70 is ubiquitously and constitutively expressed but can be stimulated by heat shock. All the facts above firmly established that the cloned cDNA fragment was a part of the cDNA encoding a Hsc70 protein in the oyster C. ariakensis .
出处 《动物学报》 SCIE CAS CSCD 北大核心 2003年第5期708-712,共5页 ACTA ZOOLOGICA SINICA
基金 国家自然科学基金(No .3 9970 5 81) 国家自然科学基金农业倾斜项目(No .3 0 170 741) 中国科学院知识创新工程重要方向项目(KSCX2 SW 3 0 2 8) 广东省科技创新百项工程资助项目(No .99B0 62 0 1G)~~
关键词 近江牡蛎 Hsc70蛋白基因 CDNA片段 克隆 SOUTHERN杂交 RT-PCR分析 Oyster ( Crassostrea ariakensis ), Hsc70 gene , cDNA sequence , Southern blotting, RT PCR
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参考文献9

  • 1Clegg, J. S., K. R. Uhlinger, S. A.Jackson, G. N. Cherr, E.Rifkin and C. S. Friedman 1998 Induced thermotolerance and theheat shock protein-70 family in the Pacific oyster Crassostrea gigas. Molecular MarineBiology and Biotechnology 7:21 ~30.
  • 2Courdon, I., L. Gricourt, K. Kellner, P. Roch and J. M. Escoubas 2000Characterization of a cDNA encoding a 72 kDa heat shock cognate protein (Hsc 72) from thePacific oyster, Crassostrea gigas. DNA Sequence 11 (3~4): 265~270.
  • 3Drew, B., D. Miller, T. Toop and P. Hanna 2001 Identification of expressed Hsp's inblacklip abalone (Haliotis rubra Leach) during heat and salinity stress. Journal ofShellfish Research 20:695~703.
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  • 5Kiang, J. G. and G. C. Tsokos 1998 Heat shock protein 70 kDa molecular biology,biochemistry, and physiology. Pharmacology and Therapeutics 80: 183~201.
  • 6Rathinam, A. V., T. T. Chen and R. M. Grossfeld 2000 Cloning and sequence analysisof a cDNA for an inducible 70 kDa heat shock protein (Hsp 70) of the American oyster(Crassostrea virginica). DNA Sequence 11: 261~264.
  • 7Sambrook, J. , E. F. Fritsch and T. Maniatis 1989 Molecular Cloning: A LaboratoryManual. 2nd edn. New York: Cold Spring Harbor Laboratory Press.
  • 8Shamseldin, A. A. , J. Clegg, C. S. Friedman, G. N. Cherr and M.C. Pillai 1997Induced thermotolerance in the Pacific oyster,Crassostrea gigas. Journal of ShellfishResearch 16: 487~491.
  • 9Tirard, C. T. , R. M. Grossfeld, J. F. Levine and S. S. Kennedy 1995 Effect ofhyperthermia in vitro on stress protein synthesis and accumulation in oyster haemocytes.Fish and Shellfish Immunology 5: 9~25.

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