Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
20
pubmed:dateCreated
2005-5-17
pubmed:databankReference
pubmed:abstractText
Cdt1 is an essential component for the assembly of a pre-replicative complex. Cdt1 activity is inhibited by geminin, which also participates in neural development and embryonic differentiation in many eukaryotes. Although Cdt1 homologues have been identified in organisms ranging from yeast to human, geminin homologues had not been described for Caenorhabditis elegans and fungi. Here, we identify the C. elegans geminin, GMN-1. Biochemical analysis reveals that GMN-1 associates with C. elegans CDT-1, the Hox protein NOB-1, and the Six protein CEH-32. GMN-1 inhibits not only the interaction between mouse Cdt1 and Mcm6 but also licensing activity in Xenopus egg extracts. RNA interference-mediated reduction of GMN-1 is associated with enlarged germ nuclei with aberrant nucleolar morphology, severely impaired gametogenesis, and chromosome bridging in intestinal cells. We conclude that the Cdt1-geminin system is conserved throughout metazoans and that geminin has evolved in these taxa to regulate proliferation and differentiation by directly interacting with Cdt1 and homeobox proteins.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Caenorhabditis elegans Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Cell Cycle Proteins, http://linkedlifedata.com/resource/pubmed/chemical/DNA, Helminth, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Mcm6 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/NOB-1 protein, C elegans, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Ris2 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/ceh-32 protein, C elegans
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
20
pubmed:volume
280
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
19689-94
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15811859-Amino Acid Sequence, pubmed-meshheading:15811859-Animals, pubmed-meshheading:15811859-Base Sequence, pubmed-meshheading:15811859-Caenorhabditis elegans, pubmed-meshheading:15811859-Caenorhabditis elegans Proteins, pubmed-meshheading:15811859-Cell Cycle, pubmed-meshheading:15811859-Cell Cycle Proteins, pubmed-meshheading:15811859-Conserved Sequence, pubmed-meshheading:15811859-DNA, Helminth, pubmed-meshheading:15811859-DNA-Binding Proteins, pubmed-meshheading:15811859-Female, pubmed-meshheading:15811859-Germ Cells, pubmed-meshheading:15811859-Homeodomain Proteins, pubmed-meshheading:15811859-Humans, pubmed-meshheading:15811859-Male, pubmed-meshheading:15811859-Mice, pubmed-meshheading:15811859-Molecular Sequence Data, pubmed-meshheading:15811859-Phenotype, pubmed-meshheading:15811859-RNA Interference, pubmed-meshheading:15811859-Recombinant Proteins, pubmed-meshheading:15811859-Sequence Homology, Amino Acid, pubmed-meshheading:15811859-Transcription Factors
pubmed:year
2005
pubmed:articleTitle
Caenorhabditis elegans geminin homologue participates in cell cycle regulation and germ line development.
pubmed:affiliation
Cellular Physiology Laboratory, Discovery Research Institute, RIKEN, Wako, Saitama, Japan.
pubmed:publicationType
Journal Article, In Vitro, Research Support, Non-U.S. Gov't