Source:http://linkedlifedata.com/resource/pubmed/id/21557657
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rdf:type | |
lifeskim:mentions |
umls-concept:C0006556,
umls-concept:C0009017,
umls-concept:C0030956,
umls-concept:C0034650,
umls-concept:C0220781,
umls-concept:C0678579,
umls-concept:C0679058,
umls-concept:C0999030,
umls-concept:C1136254,
umls-concept:C1547699,
umls-concept:C1556094,
umls-concept:C1709634,
umls-concept:C1880022,
umls-concept:C2700640
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pubmed:issue |
5
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pubmed:dateCreated |
2011-5-11
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pubmed:abstractText |
Using a combination of reverse-transcription polymerase chain reaction and the 5'- and/or 3'-rapid amplification of cDNA ends, we cloned, from a Japanese brown frog (Rana japonica) skin total RNA preparation, cDNAs encoding biosynthetic precursors for the antimicrobial peptides (AMPs) japonicin-1Ja (FFPIGVFCKIFKTC), japonicin-2Ja (FGLPMLSILPKALCILLKRKC), and temporin-1Ja (ILPLVGNLLNDLL.NH2). These peptides were previously isolated from an extract of R. japonica skin. The present study is the first report to describe the molecular cloning of the cDNA encoding a japonicin-2 family peptide. The nucleotide and deduced amino acid sequence analyses revealed that the hypothetical precursor protein of japonicin-2Ja, as well as japonicin-1Ja and temporin-1Ja, is organized similarly to those of typical amphibian AMP precursors, with a highly conserved signal peptide, a relatively well conserved intervening sequence, and a hypervariable AMP mature region. Antimicrobial assays for synthetic replicates of cyclic and linear japonicin-2Ja revealed that the intramolecular disulfide bond is necessary for activity. A semi-quantitative analysis by real-time RTPCR using TaqMan probes revealed that the relative values of preprojaponicin-2Ja mRNA expression levels in the skin, skeletal muscle of hind leg, kidney, testis, small intestine, and stomach total RNA sample specimens in adult R. japonica were 6.5×10(5), 9.6, 2.0, 1.6, 1.6, and 1.0, respectively. The presence of preprojaponicin-2Ja mRNAs in the cytoplasm of glandular cells in R. japonica dorsal skin glands was demonstrated by means of in situ hybridization using digoxigenin-labeled cRNA probes for the precursor.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0289-0003
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
339-47
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pubmed:meshHeading |
pubmed-meshheading:21557657-Amino Acid Sequence,
pubmed-meshheading:21557657-Animals,
pubmed-meshheading:21557657-Anti-Infective Agents,
pubmed-meshheading:21557657-Base Sequence,
pubmed-meshheading:21557657-Cloning, Molecular,
pubmed-meshheading:21557657-DNA, Complementary,
pubmed-meshheading:21557657-Gene Expression Regulation,
pubmed-meshheading:21557657-Molecular Sequence Data,
pubmed-meshheading:21557657-RNA, Messenger,
pubmed-meshheading:21557657-Ranidae
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pubmed:year |
2011
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pubmed:articleTitle |
Molecular cloning and characterization of cDNAs encoding biosynthetic precursors for the antimicrobial peptides japonicin-1Ja, japonicin-2Ja, and temporin-1Ja in the Japanese brown frog, Rana japonica.
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pubmed:affiliation |
Department of Biology, Faculty of Science, Toho University, 2-2-1 Miyama, Funabashi, Chiba 274-8510, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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