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Molecular cloning and expression analysis of a pearl oyster (Pinctada martensii) heat shock protein 90 (HSP90)  ( SCI-EXPANDED收录)   被引量:13

文献类型:期刊文献

英文题名:Molecular cloning and expression analysis of a pearl oyster (Pinctada martensii) heat shock protein 90 (HSP90)

作者:Liang, H. Y.[1];Wang, Z. X.[1];Lei, Q. N.[1];Huang, R. L.[1];Deng, Y. W.[1];Wang, Q. H.[1];Jiao, Y.[1];Du, X. D.[1]

机构:[1]Guangdong Ocean Univ, Coll Fisheries, Zhanjiang, Peoples R China

年份:2015

卷号:14

期号:4

起止页码:18778

外文期刊名:GENETICS AND MOLECULAR RESEARCH

收录:SCI-EXPANDED(收录号:WOS:000371587400156)、、Scopus(收录号:2-s2.0-84952788394)、WOS

基金:Research supported by the National Natural Science Foundation of China (#31472306), the Science and Technology Program of Guangdong, China (#2012A031100010), and the Science and Technology Program of Zhanjiang, China (#2013A03022).

语种:英文

外文关键词:Heat shock protein 90 (HSP90); Pinctada martensii; Cloning; Expression; Stress

外文摘要:Heat shock protein 90 (HSP90) is an important molecular chaperone required for proper folding of cellular proteins, and thus, it plays an essential role in protecting cells from damage during stress. In this study, an HSP90 cDNA designated PmHSP90 was cloned from the mantle tissue of the pearl oyster Pinctada martensii using reverse transcription polymerase chain reaction (RT-PCR) coupled with the rapid amplification of cDNA ends (RACE) approach. PmHSP90 cDNA was 2584 bp in length, including an open reading frame of 2160 bp, which encodes a polypeptide of 719 amino acid residues, with predicted molecular mass and isoelectric point of 83.0 kDa and 4.87, respectively. Multiple-sequence alignment indicated that HSP90 is highly conserved among species, and PmHSP90 showed 89% sequence identity to Crassostrea gigas HSP90. Five conserved amino acid blocks defined as HSP90 protein family signatures were also observed in PmHSP90, indicating that PmHSP90 may be a cytosolic member of the HSP90 family. Expression levels of PmHSP90 were detected in various tissues of P. martensii and in hemocytes under three different stress conditions using quantitative real-time PCR (qPCR). The results demonstrate that PmHSP90 mRNA is constitutively expressed in all the tested tissues and may be involved in the immune response against thermal stress, lipopolysaccharide stimulation, and nucleus insertion operations. Studies on PmHSP90 are a valuable source to further explore the immune system in pearl oysters during the production of pearls, and may enhance our knowledge of molluscan innate immunity.

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