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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1992-3-11
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pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D10555,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D10556,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D13201,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D13202,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/D13203,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M94783,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M94784,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M94785,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X62976,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X62977
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pubmed:abstractText |
The proliferating cell-nuclear antigen (PCNA) plays a key role in the control of eukaryotic DNA replication. We have isolated two cross-hybridizing groups of cDNA encoding carrot homologs of PCNA. Sequence analysis and Southern-blot experiments showed that the cDNA were derived from two distinct genes. One corresponded to the typical PCNA, which is known to be highly conserved in eukaryotes from yeast to man; its mRNA is 1.2 kb in size and the calculated molecular mass of the protein is 29 kDa. The other encoded a larger PCNA homolog which has not previously been reported; the mRNA is 1.5 kb in size, the N-terminal three quarters (calculated molecular mass, 29 kDa) of the protein product is 88% identical at the amino acid level to the typical PCNA, but the protein has an extra C-terminal domain of 11 kDa. Both PCNA homologs were apparently coexpressed concomitant with somatic embryogenesis. The mRNA level of the novel homolog is 10-20% that of the typical PCNA in the embryos. The presence of the second putative PCNA may provide new insight into studies on the mechanism of DNA replication in eukaryotes.
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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 |
Feb
|
pubmed:issn |
0014-2956
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
|
pubmed:volume |
203
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
367-71
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pubmed:dateRevised |
2007-7-23
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pubmed:meshHeading |
pubmed-meshheading:1346518-Amino Acid Sequence,
pubmed-meshheading:1346518-Base Sequence,
pubmed-meshheading:1346518-Blotting, Southern,
pubmed-meshheading:1346518-Cloning, Molecular,
pubmed-meshheading:1346518-DNA,
pubmed-meshheading:1346518-Molecular Sequence Data,
pubmed-meshheading:1346518-Nuclear Proteins,
pubmed-meshheading:1346518-Proliferating Cell Nuclear Antigen,
pubmed-meshheading:1346518-Protein Biosynthesis,
pubmed-meshheading:1346518-RNA, Messenger,
pubmed-meshheading:1346518-Sequence Homology, Nucleic Acid,
pubmed-meshheading:1346518-Vegetables
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pubmed:year |
1992
|
pubmed:articleTitle |
Identification of carrot cDNA clones encoding a second putative proliferating cell-nuclear antigen, DNA polymerase delta auxiliary protein.
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pubmed:affiliation |
National Institute of Agrobiological Resources, Ibaraki, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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