Screening and analysis of PoAkirin1 and two related genes in response to immunological stimulants in the Japanese flounder (Paralichthys olivaceus)
A member of the NF-κB signaling pathway, PoAkirin1, was cloned from a full-length cDNA library of Japanese flounder (Paralichthys olivaceus). The full-length cDNA comprises a 5′UTR of 202 bp, an open reading frame of 564 bp encoding a 187-amino-acid polypeptide and a 521-bp 3′UTR with a poly (A) tai...
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ftpubmed:oai:pubmedcentral.nih.gov:3700861 2023-05-15T18:15:49+02:00 Screening and analysis of PoAkirin1 and two related genes in response to immunological stimulants in the Japanese flounder (Paralichthys olivaceus) Yang, Chang-Geng Wang, Xian-Li Zhang, Bo Sun, Bing Liu, Shan-Shan Chen, Song-Lin 2013-05-07 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700861 http://www.ncbi.nlm.nih.gov/pubmed/23651673 https://doi.org/10.1186/1471-2199-14-10 en eng BioMed Central http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700861 http://www.ncbi.nlm.nih.gov/pubmed/23651673 http://dx.doi.org/10.1186/1471-2199-14-10 Copyright ©2013 Yang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. CC-BY Research Article Text 2013 ftpubmed https://doi.org/10.1186/1471-2199-14-10 2013-09-05T01:58:56Z A member of the NF-κB signaling pathway, PoAkirin1, was cloned from a full-length cDNA library of Japanese flounder (Paralichthys olivaceus). The full-length cDNA comprises a 5′UTR of 202 bp, an open reading frame of 564 bp encoding a 187-amino-acid polypeptide and a 521-bp 3′UTR with a poly (A) tail. The putative protein has a predicted molecular mass of 21 kDa and an isoelectric point (pI) of 9.22. Amino acid sequence alignments showed that PoAkirin1 was 99% identical to the Scophthalmus maximus Akirin protein (ADK27484). Yeast two-hybrid assays identified two proteins that interact with PoAkirin1: PoHEPN and PoC1q. The cDNA sequences of PoHEPN and PoC1q are 672 bp and 528 bp, respectively. Real-time quantitative reverse-transcriptase polymerase chain reaction analysis showed that bacteria could induce the expressions of PoAkirin1, PoHEPN and PoC1q. However, the responses of PoHEPN and PoC1q to the bacterial challenge were slower than that of PoAkirin1. To further study the function of PoAkirin1, recombinant PoAkirin1 and PoHEPN were expressed in Escherichia coli and would be used to verify the PoAkirin1-PoHEPN binding activity. These results identified two proteins that potentially interact with PoAkirin1 and that bacteria could induce their expression. Text Scophthalmus maximus PubMed Central (PMC) BMC Molecular Biology 14 1 10 |
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Research Article Yang, Chang-Geng Wang, Xian-Li Zhang, Bo Sun, Bing Liu, Shan-Shan Chen, Song-Lin Screening and analysis of PoAkirin1 and two related genes in response to immunological stimulants in the Japanese flounder (Paralichthys olivaceus) |
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Research Article |
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A member of the NF-κB signaling pathway, PoAkirin1, was cloned from a full-length cDNA library of Japanese flounder (Paralichthys olivaceus). The full-length cDNA comprises a 5′UTR of 202 bp, an open reading frame of 564 bp encoding a 187-amino-acid polypeptide and a 521-bp 3′UTR with a poly (A) tail. The putative protein has a predicted molecular mass of 21 kDa and an isoelectric point (pI) of 9.22. Amino acid sequence alignments showed that PoAkirin1 was 99% identical to the Scophthalmus maximus Akirin protein (ADK27484). Yeast two-hybrid assays identified two proteins that interact with PoAkirin1: PoHEPN and PoC1q. The cDNA sequences of PoHEPN and PoC1q are 672 bp and 528 bp, respectively. Real-time quantitative reverse-transcriptase polymerase chain reaction analysis showed that bacteria could induce the expressions of PoAkirin1, PoHEPN and PoC1q. However, the responses of PoHEPN and PoC1q to the bacterial challenge were slower than that of PoAkirin1. To further study the function of PoAkirin1, recombinant PoAkirin1 and PoHEPN were expressed in Escherichia coli and would be used to verify the PoAkirin1-PoHEPN binding activity. These results identified two proteins that potentially interact with PoAkirin1 and that bacteria could induce their expression. |
format |
Text |
author |
Yang, Chang-Geng Wang, Xian-Li Zhang, Bo Sun, Bing Liu, Shan-Shan Chen, Song-Lin |
author_facet |
Yang, Chang-Geng Wang, Xian-Li Zhang, Bo Sun, Bing Liu, Shan-Shan Chen, Song-Lin |
author_sort |
Yang, Chang-Geng |
title |
Screening and analysis of PoAkirin1 and two related genes in response to immunological stimulants in the Japanese flounder (Paralichthys olivaceus) |
title_short |
Screening and analysis of PoAkirin1 and two related genes in response to immunological stimulants in the Japanese flounder (Paralichthys olivaceus) |
title_full |
Screening and analysis of PoAkirin1 and two related genes in response to immunological stimulants in the Japanese flounder (Paralichthys olivaceus) |
title_fullStr |
Screening and analysis of PoAkirin1 and two related genes in response to immunological stimulants in the Japanese flounder (Paralichthys olivaceus) |
title_full_unstemmed |
Screening and analysis of PoAkirin1 and two related genes in response to immunological stimulants in the Japanese flounder (Paralichthys olivaceus) |
title_sort |
screening and analysis of poakirin1 and two related genes in response to immunological stimulants in the japanese flounder (paralichthys olivaceus) |
publisher |
BioMed Central |
publishDate |
2013 |
url |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700861 http://www.ncbi.nlm.nih.gov/pubmed/23651673 https://doi.org/10.1186/1471-2199-14-10 |
genre |
Scophthalmus maximus |
genre_facet |
Scophthalmus maximus |
op_relation |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3700861 http://www.ncbi.nlm.nih.gov/pubmed/23651673 http://dx.doi.org/10.1186/1471-2199-14-10 |
op_rights |
Copyright ©2013 Yang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
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CC-BY |
op_doi |
https://doi.org/10.1186/1471-2199-14-10 |
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BMC Molecular Biology |
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