The role of EaIκB-α, an IκB-α homologue in Epinephelus akaara, involved in innate immune response
Biotechnology Letters, ISSN: 1573-6776, Vol: 36, Issue: 7, Page: 1421-1429
2014
- 2Citations
- 5Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations2
- Citation Indexes2
- CrossRef1
- Captures5
- Readers5
Article Description
The inhibitor κB (IκB) protein is an important component of the nuclear factor kB (NF-κB) signaling pathway. We have cloned and characterized the IκB-α homologue gene (named EaIκB-α) from grouper (Epinephelus akaara), expressed it in Escherichia coli and generated a rabbit polyclonal antibody. EaIκB-α encodes a 308-amino acid protein with evolutionarily and functionally homology to mammalian IκB-α. Over-expression of wild-type EaIκB-α or a mutated, nondegradable EaIκB-α (EaIκB-αM) in Escherichia coli both inhibited the degradation of cellular EaIκB-α, activation of NF-κB and expression of tumor necrosis factor α (TNF-α). EaIκB-α protein is restricted to the cytoplasm in unstimulated cell. Activated by diverse stimuli, EaIκB-α is degraded, thereby releasing NF-κB into nucleus and activating NF-κB-mediated transcripts. EaIκB-α and other studied NF-κB target genes are induced by LPS in kidney and liver, which suggests that EaIκB-α may play an important role in immune response of grouper. © 2014 Springer Science+Business Media Dordrecht.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84902278114&origin=inward; http://dx.doi.org/10.1007/s10529-014-1496-3; http://www.ncbi.nlm.nih.gov/pubmed/24658739; http://link.springer.com/10.1007/s10529-014-1496-3; https://dx.doi.org/10.1007/s10529-014-1496-3; https://link.springer.com/article/10.1007/s10529-014-1496-3
Springer Science and Business Media LLC
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