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AS-hepc2

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AS-hepc2 is an antimicrobial peptide produced by Acanthopagrus schlegelii (Black porgy). It has antimicrobial activity.

Category
Functional Peptides
Catalog number
BAT-013036
Molecular Formula
C98H148N34O27S9
Molecular Weight
2523.01
Synonyms
Hepcidin AS-hepc2; Ser-Pro-Ala-Gly-Cys-Arg-Phe-Cys-Cys-Gly-Cys-Cys-Pro-Asn-Met-Arg-Gly-Cys-Gly-Val-Cys-Cys-Arg-Phe (Disulfide bridge: Cys5-Cys22, Cys8-Cys21, Cys9-Cys18, Cys11-Cys12)
Purity
>98%
Sequence
SPAGCRFCCGCCPNMRGCGVCCRF (Disulfide bridge: Cys5-Cys22, Cys8-Cys21, Cys9-Cys18, Cys11-Cys12)
1. Hepcidin gene expression induced in the developmental stages of fish upon exposure to Benzo[a]pyrene (BaP)
Ke-Jian Wang, Jun Bo, Ming Yang, Hua-Sheng Hong, Xin-Hong Wang, Fang-Yi Chen, Jian-Jun Yuan Mar Environ Res. 2009 Apr;67(3):159-65. doi: 10.1016/j.marenvres.2008.12.008. Epub 2008 Dec 30.
Hepcidin is known to be expressed in fish with bacterial challenge and iron overload. Here we first report the hepcidin expression induced in the developmental stages from embryo to fry of red sea bream (Pagarus major) and in juvenile black porgy (Acanthopagrus schlegelii B.) upon continuous waterborne exposure to BaP. The gene expression of CYP1A1 and IgL (immunoglobulin light chain) were both measured. Expression of the Pagarus major hepcidin gene (PM-hepc) was increased in post hatch fry at 24 h and 120 h exposure to BaP at concentrations of 0.1, 0.5 and 1.0 microg/l, respectively. The gene expression pattern was comparable to that of CYP1A1 but different from that of IgL. In addition, a high number of AS-hepc2 transcripts (Acanthopagrus schlegelii B. hepcidin gene) were detected in the liver upon exposure to 1.0 microg/l BaP. This study demonstrates that hepcidin gene expression is significantly induced in BaP-exposed red sea bream and black porgy.
2. Molecular characterization of hepcidin AS-hepc2 and AS-hepc6 in black porgy (Acanthopagrus schlegelii): expression pattern responded to bacterial challenge and in vitro antimicrobial activity
Ming Yang, Bei Chen, Jing-Jing Cai, Hui Peng, Ling-Cai, Jian-Jun Yuan, Ke-Jian Wang Comp Biochem Physiol B Biochem Mol Biol. 2011 Feb;158(2):155-63. doi: 10.1016/j.cbpb.2010.11.003. Epub 2010 Nov 10.
There are more diversified isoforms of the hepcidin gene that exist in fishes than in mammals, and elucidating the differences between these isoforms should provide insight into the functioning of hepcidin in fishes. In our study, AS-hepc2 and AS-hepc6 hepcidin isoforms from black porgy were characterized for their in vivo expression patterns following bacterial challenge, and their in vitro antimicrobial activities against Gram-positive and Gram-negative bacteria as well as fungi. As a result, two isoforms were observed to be widely distributed in all the tissues tested. AS-hepc2 was a liver-expressed hepcidin peptide which was always highly more expressed in the liver than in the other tissues tested no matter whether this was before or after bacterial challenge. AS-hepc6 was detected mainly in the head kidney and trunk kidney of normal fish, but, in the challenged fish, its expression involved more tissues than just the kidneys. The mature peptides of AS-hepc2 and AS-hepc6 were modeled for 3D structure and then synthesized for antimicrobial assay. AS-hepc6 had a wider antimicrobial spectrum than AS-hepc2 and, in particular, had more potent antifungal activity. Our study indicated that the two hepcidin isoforms had different characteristics in terms of their expression patterns and antimicrobial activity, and they were assumed to play an overlapping role in the innate immune system of black porgy against invading pathogens.
3. Genomic organization and tissue-specific expression analysis of hepcidin-like genes from black porgy (Acanthopagrus schlegelii B)
Ming Yang, Ke-Jian Wang, Jun-Hui Chen, Hai-Dong Qu, Shao-Jing Li Fish Shellfish Immunol. 2007 Nov;23(5):1060-71. doi: 10.1016/j.fsi.2007.04.011. Epub 2007 May 13.
Hepcidin is an antimicrobial peptide and putative iron regulatory hormone previously described in mice and humans. Dozens of fish hepcidins have been isolated and characterized so far. Here we present seven hepcidin-like cDNA sequences named AS-hepc1-7, amplified from the normal commercially cultured fish (black porgy) by RACE-PCR. Sequence analysis reveals that these seven potential hepcidin peptides have highly conserved sequences with other known hepcidins, but they are different from each other in constitution and characteristics of predicted mature amino acids. Based on the study, it is deduced that AS-hepc1-7 represent different variants of a family of hepcidin genes in black porgy. To understand the organization of these hepcidin-like genes, we sequenced AS-hepc2 DNA, AS-hepc3 DNA, AS-hepc4 DNA, AS-hepc7 DNA and AS-hepc2 upstream region; and all of the four genomic DNAs consisted of two introns and three exons, the same organization as other reported hepcidins. The tissue-specific gene expression of hepcidins in normal black porgy was evaluated using RT-PCR and dot blot approaches. RT-PCR showed that transcripts of hepcidin-like mRNAs were present in each tested tissue of normal juvenile black porgy, including liver, spleen, kidney, heart, brain, stomach, intestine, gill, skin and blood, but abundant hepcidin-like mRNA transcripts were only detected in the liver, kidney, spleen, intestine and stomach by dot blot assay. In addition, using dot blot and Northern blot approach, a significant increase of hepcidin mRNA transcription was observed in the liver within 48 h after immersion in a suspension of live bacteria, which suggested that the expression pattern of hepcidin-like genes in black porgy might be different in the liver from the other tissues as previously reported in several hepcidin studies.
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