Source:http://linkedlifedata.com/resource/pubmed/id/18339999
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2008-3-14
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pubmed:databankReference | |
pubmed:abstractText |
Divalent metal transporter 1 (DMT1) is an electrogenic transporter of divalent Mn that is expressed at a high level on the brush-border membrane of enterocytes. This study is the first reported isolation of the 2 full-length cDNA sequences of the small intestinal DMT1 gene of broilers by rapid amplification of cDNA ends. The chicken DMT1 isoform I cDNA was 1,972 bp and contained a 1,695-bp open reading frame encoding a 564-amino acid protein, and the chicken DMT1 isoform II cDNA was 1,775 bp and contained a 1,593-bp open reading frame encoding a 530-amino acid protein. The 2 chicken DMT1 isoform transcripts differed in their 3'-translated regions and untranslated regions. The identities of the amino acid sequence deduced from the full-length cDNA sequence of the chicken DMT1 isoform I with DMT1 not containing the iron-responsive element of the mouse, rat, and human were 82, 82, and 80%, respectively. The identities of the amino acid sequence deduced from the full-length cDNA sequence of the chicken DMT1 isoform II with those of the mouse, rat, and human were 84, 84, and 83%, respectively. Analyses of hydrophobicity, transmembrane region, and signal peptides of DMT1 proteins deduced by nucleotide sequences suggested that chicken DMT1 isoforms are transmembrane proteins with several conserved peptide sequences, such as N-linked glycosylation signals (N-X-S/ T, where X designates any amino acid) and the consensus transport motif. The total mRNA levels of the 2 chicken DMT1 isoforms, the mRNA levels of chicken DMT1 isoform I, and the mRNA levels of chicken DMT1 isoform II in the duodenum and jejunum were higher (P<0.002) than that in the ileum by real-time reverse transcription PCR assay. There was no significant difference (P>0.26) between the duodenum and jejunum for the above 3 indices. The mRNA level of the chicken DMT1 isoform I was higher (P<0.001) than that of the chicken DMT1 isoform II in each small intestinal segment of Mn-deficient broilers.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cation Transport Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/Manganese,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Isoforms,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/solute carrier family 11-...
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0032-5791
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
87
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
768-76
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:18339999-Amino Acid Sequence,
pubmed-meshheading:18339999-Animals,
pubmed-meshheading:18339999-Base Sequence,
pubmed-meshheading:18339999-Cation Transport Proteins,
pubmed-meshheading:18339999-Chickens,
pubmed-meshheading:18339999-Cloning, Molecular,
pubmed-meshheading:18339999-DNA, Complementary,
pubmed-meshheading:18339999-Hydrophobic and Hydrophilic Interactions,
pubmed-meshheading:18339999-Intestine, Small,
pubmed-meshheading:18339999-Male,
pubmed-meshheading:18339999-Manganese,
pubmed-meshheading:18339999-Molecular Sequence Data,
pubmed-meshheading:18339999-Protein Isoforms,
pubmed-meshheading:18339999-RNA, Messenger,
pubmed-meshheading:18339999-Random Amplified Polymorphic DNA Technique,
pubmed-meshheading:18339999-Sequence Alignment
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pubmed:year |
2008
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pubmed:articleTitle |
Cloning, sequencing, characterization, and expressions of divalent metal transporter one in the small intestine of broilers.
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pubmed:affiliation |
Mineral Nutrition Research Division, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100094, PR China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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