Molecular cloning of two tandemly arranged peroxidase genes from Populus kitakamiensis and their differential regulation in the stem.
Identifieur interne : 004A78 ( Main/Corpus ); précédent : 004A77; suivant : 004A79Molecular cloning of two tandemly arranged peroxidase genes from Populus kitakamiensis and their differential regulation in the stem.
Auteurs : K. Osakabe ; H. Koyama ; S. Kawai ; Y. Katayama ; N. MorohoshiSource :
- Plant molecular biology [ 0167-4412 ] ; 1995.
English descriptors
- KwdEn :
- Amino Acid Sequence (MeSH), Base Sequence (MeSH), Blotting, Northern (MeSH), Blotting, Southern (MeSH), Gene Dosage (MeSH), Genomic Library (MeSH), Isoenzymes (biosynthesis), Isoenzymes (genetics), Lignin (biosynthesis), Molecular Sequence Data (MeSH), Multigene Family (genetics), Peroxidases (biosynthesis), Peroxidases (genetics), Plant Stems (enzymology), Promoter Regions, Genetic (genetics), Sequence Analysis, DNA (MeSH), Sequence Homology, Amino Acid (MeSH), Transcription, Genetic (MeSH), Trees (genetics).
- MESH :
- chemical , biosynthesis : Isoenzymes, Lignin, Peroxidases.
- chemical , genetics : Isoenzymes, Peroxidases.
- enzymology : Plant Stems.
- genetics : Multigene Family, Promoter Regions, Genetic, Trees.
- Amino Acid Sequence, Base Sequence, Blotting, Northern, Blotting, Southern, Gene Dosage, Genomic Library, Molecular Sequence Data, Sequence Analysis, DNA, Sequence Homology, Amino Acid, Transcription, Genetic.
Abstract
A genomic library was prepared from Populus kitakamiensis and screened with the cDNA for an anionic peroxidase from P. kitakamiensis. One genomic clone was isolated that contained two tandemly oriented genes for anionic peroxidases, prxA3a and prxA4a. Both genes consisted of four exons and three introns; the introns had consensus nucleotides, namely, GT and AG, at their 5' and 3' ends, respectively. The prxA3a and prxA4a genes encoded 347 and 343 amino acid residues, respectively, including putative signal sequences at the amino-termini. Putative promoters and polyadenylation signals were found in the flanking regions of both genes. The sequence of the coding region of prxA3a was completely identical to that of the cDNA clone pA3, whereas the sequence of the coding region of prxA4a was only 73% identical to that of the cDNA clone pA3. Northern blot analysis showed that the patterns of expression of the mRNAs that corresponded to prxA3a and prxA4a differed in stems of P. kitakamiensis.
DOI: 10.1007/BF00021193
PubMed: 7647300
Links to Exploration step
pubmed:7647300Le document en format XML
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<affiliation><nlm:affiliation>Laboratory of Wood Chemistry, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Japan.</nlm:affiliation>
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<author><name sortKey="Koyama, H" sort="Koyama, H" uniqKey="Koyama H" first="H" last="Koyama">H. Koyama</name>
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<author><name sortKey="Kawai, S" sort="Kawai, S" uniqKey="Kawai S" first="S" last="Kawai">S. Kawai</name>
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<author><name sortKey="Katayama, Y" sort="Katayama, Y" uniqKey="Katayama Y" first="Y" last="Katayama">Y. Katayama</name>
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<author><name sortKey="Morohoshi, N" sort="Morohoshi, N" uniqKey="Morohoshi N" first="N" last="Morohoshi">N. Morohoshi</name>
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<author><name sortKey="Osakabe, K" sort="Osakabe, K" uniqKey="Osakabe K" first="K" last="Osakabe">K. Osakabe</name>
<affiliation><nlm:affiliation>Laboratory of Wood Chemistry, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Japan.</nlm:affiliation>
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<author><name sortKey="Koyama, H" sort="Koyama, H" uniqKey="Koyama H" first="H" last="Koyama">H. Koyama</name>
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<author><name sortKey="Kawai, S" sort="Kawai, S" uniqKey="Kawai S" first="S" last="Kawai">S. Kawai</name>
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<author><name sortKey="Katayama, Y" sort="Katayama, Y" uniqKey="Katayama Y" first="Y" last="Katayama">Y. Katayama</name>
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<author><name sortKey="Morohoshi, N" sort="Morohoshi, N" uniqKey="Morohoshi N" first="N" last="Morohoshi">N. Morohoshi</name>
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<series><title level="j">Plant molecular biology</title>
<idno type="ISSN">0167-4412</idno>
<imprint><date when="1995" type="published">1995</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Amino Acid Sequence (MeSH)</term>
<term>Base Sequence (MeSH)</term>
<term>Blotting, Northern (MeSH)</term>
<term>Blotting, Southern (MeSH)</term>
<term>Gene Dosage (MeSH)</term>
<term>Genomic Library (MeSH)</term>
<term>Isoenzymes (biosynthesis)</term>
<term>Isoenzymes (genetics)</term>
<term>Lignin (biosynthesis)</term>
<term>Molecular Sequence Data (MeSH)</term>
<term>Multigene Family (genetics)</term>
<term>Peroxidases (biosynthesis)</term>
<term>Peroxidases (genetics)</term>
<term>Plant Stems (enzymology)</term>
<term>Promoter Regions, Genetic (genetics)</term>
<term>Sequence Analysis, DNA (MeSH)</term>
<term>Sequence Homology, Amino Acid (MeSH)</term>
<term>Transcription, Genetic (MeSH)</term>
<term>Trees (genetics)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Isoenzymes</term>
<term>Lignin</term>
<term>Peroxidases</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Isoenzymes</term>
<term>Peroxidases</term>
</keywords>
<keywords scheme="MESH" qualifier="enzymology" xml:lang="en"><term>Plant Stems</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Multigene Family</term>
<term>Promoter Regions, Genetic</term>
<term>Trees</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Amino Acid Sequence</term>
<term>Base Sequence</term>
<term>Blotting, Northern</term>
<term>Blotting, Southern</term>
<term>Gene Dosage</term>
<term>Genomic Library</term>
<term>Molecular Sequence Data</term>
<term>Sequence Analysis, DNA</term>
<term>Sequence Homology, Amino Acid</term>
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<front><div type="abstract" xml:lang="en">A genomic library was prepared from Populus kitakamiensis and screened with the cDNA for an anionic peroxidase from P. kitakamiensis. One genomic clone was isolated that contained two tandemly oriented genes for anionic peroxidases, prxA3a and prxA4a. Both genes consisted of four exons and three introns; the introns had consensus nucleotides, namely, GT and AG, at their 5' and 3' ends, respectively. The prxA3a and prxA4a genes encoded 347 and 343 amino acid residues, respectively, including putative signal sequences at the amino-termini. Putative promoters and polyadenylation signals were found in the flanking regions of both genes. The sequence of the coding region of prxA3a was completely identical to that of the cDNA clone pA3, whereas the sequence of the coding region of prxA4a was only 73% identical to that of the cDNA clone pA3. Northern blot analysis showed that the patterns of expression of the mRNAs that corresponded to prxA3a and prxA4a differed in stems of P. kitakamiensis.</div>
</front>
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<Issue>4</Issue>
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<Title>Plant molecular biology</Title>
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<ArticleTitle>Molecular cloning of two tandemly arranged peroxidase genes from Populus kitakamiensis and their differential regulation in the stem.</ArticleTitle>
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<Abstract><AbstractText>A genomic library was prepared from Populus kitakamiensis and screened with the cDNA for an anionic peroxidase from P. kitakamiensis. One genomic clone was isolated that contained two tandemly oriented genes for anionic peroxidases, prxA3a and prxA4a. Both genes consisted of four exons and three introns; the introns had consensus nucleotides, namely, GT and AG, at their 5' and 3' ends, respectively. The prxA3a and prxA4a genes encoded 347 and 343 amino acid residues, respectively, including putative signal sequences at the amino-termini. Putative promoters and polyadenylation signals were found in the flanking regions of both genes. The sequence of the coding region of prxA3a was completely identical to that of the cDNA clone pA3, whereas the sequence of the coding region of prxA4a was only 73% identical to that of the cDNA clone pA3. Northern blot analysis showed that the patterns of expression of the mRNAs that corresponded to prxA3a and prxA4a differed in stems of P. kitakamiensis.</AbstractText>
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