ArticleMolecular biology reports2009
Molecular cloning, characterization and mRNA expression of peroxiredoxin in Zhikong scallop Chlamys farreri.
Article in Molecular biology reports, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
What it found
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Who cites it
7 citing papers in PubMed, 28 citations in OpenAlex.
- Effects of heavy metals on the expression of a zinc-inducible metallothionein-III gene and antioxidant enzyme activities in Crassostrea gigas.Ecotoxicology (London, England) · 2012Article
- Identification and expression of a putative LPS-induced TNF-α factor from Asiatic hard clam Meretrix meretrix.Molecular biology reports · 2012Article
- Cloning, expression and dynamic simulation of TRYP6 from Leishmania major (MRHO/IR/75/ER).Molecular biology reports · 2011Article
- Cloning and characterization of two ferritin subunit genes from bay scallop, Argopecten irradians (Lamarck 1819).Molecular biology reports · 2011Article
- Recombinant expression, characterization and expressional analysis of clam Meretrix meretrix cathepsin B, an enzyme involved in nutrient digestion.Molecular biology reports · 2011Article
- Identification of host-defense genes and development of microsatellite markers from ESTs of hard clam Meretrix meretrix.Molecular biology reports · 2011Article
- Molecular cloning and mRNA expression of peroxiredoxin gene in black tiger shrimp (Penaeus monodon).Molecular biology reports · 2010Article
Corrections and comments
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Peroxiredoxin V (PRX V) is known as an atypical 2-cysteine peroxiredoxin that protects the organisms against various oxidative stresses and functions in signal transduction. The cDNA of a PRX V gene (designated as CfPRX) was cloned from scallop Chlamys farreri. The full-length sequence of CfPRX cDNA was of 2,179 bp with a 564 bp open reading frame encoding a peptide of 187 amino acids. Sequence comparison showed that CfPRX shared higher identities with PRX Vs than that with other isoforms of PRX, indicating CfPRX was a member of the PRX V family. Fluorescent real-time quantitative PCR analysis revealed the presence of CfPRX transcripts in gill filaments, adductor muscle, heart, gonad, kidney and hemocytes, and the stimulation of Listonella anguillarum significantly (P < 0.01) enhanced the mRNA expression of CfPRX in hemocyte. These results indicated that CfPRX was a constitutive and inducible acute-phase protein which was involved in the immune resistance to L. anguillarum stimulation.
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