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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
1998-11-4
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pubmed:databankReference |
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pubmed:abstractText |
The genes of the myc/max/mad family play an important role in controlling cell proliferation and differentiation. We have identified the first homologues of the mad and max genes in the nematode C. elegans, which we have named mdl-1 and mxl-1 respectively. Like the vertebrate MAD proteins, MDL-1 binds an E-box DNA sequence (CACGTG) when dimerized with MXL-1. However, unlike vertebrate MAX, MXL-1 can not form homodimers and bind to DNA alone. Promoter fusions to a GFP reporter suggest that these genes are coexpressed in posterior intestinal and post-mitotic neuronal cells during larval development. The coexpression in the posterior intestinal cells occurs before their final division at the end of the L1 stage and persists afterwards, demonstrating that mad and max expression can be correlated directly to the cell cycle state of an individual cell type. These data also show that mxl-1 is an obligate partner for mdl-1 in vivo and in vitro and indicate that these genes may play an important role in post-embryonic development. Finally, MDL-1 can suppress activated c-MYC/RAS-induced focus formation in a rat embryo fibroblast transformation assay. Like the vertebrate MAD protein, MDL-1 activity in suppressing transformation is dependent on a functional SIN3 interaction domain.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Basic Helix-Loop-Helix Leucine...,
http://linkedlifedata.com/resource/pubmed/chemical/Basic-Leucine Zipper Transcription...,
http://linkedlifedata.com/resource/pubmed/chemical/Caenorhabditis elegans Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Helminth Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Max protein, rat,
http://linkedlifedata.com/resource/pubmed/chemical/Myc associated factor X,
http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0950-9232
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
3
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pubmed:volume |
17
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1109-18
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:9764821-Amino Acid Sequence,
pubmed-meshheading:9764821-Animals,
pubmed-meshheading:9764821-Basic Helix-Loop-Helix Leucine Zipper Transcription Factors,
pubmed-meshheading:9764821-Basic-Leucine Zipper Transcription Factors,
pubmed-meshheading:9764821-Binding Sites,
pubmed-meshheading:9764821-Caenorhabditis elegans,
pubmed-meshheading:9764821-Caenorhabditis elegans Proteins,
pubmed-meshheading:9764821-Cell Transformation, Neoplastic,
pubmed-meshheading:9764821-DNA,
pubmed-meshheading:9764821-DNA, Complementary,
pubmed-meshheading:9764821-DNA-Binding Proteins,
pubmed-meshheading:9764821-Dimerization,
pubmed-meshheading:9764821-Gene Expression Regulation, Developmental,
pubmed-meshheading:9764821-Genes, Helminth,
pubmed-meshheading:9764821-Genes, Tumor Suppressor,
pubmed-meshheading:9764821-Genes, myc,
pubmed-meshheading:9764821-Genes, ras,
pubmed-meshheading:9764821-Helminth Proteins,
pubmed-meshheading:9764821-Intestines,
pubmed-meshheading:9764821-Larva,
pubmed-meshheading:9764821-Mitosis,
pubmed-meshheading:9764821-Molecular Sequence Data,
pubmed-meshheading:9764821-Neurons,
pubmed-meshheading:9764821-Protein Binding,
pubmed-meshheading:9764821-Protein Structure, Tertiary,
pubmed-meshheading:9764821-Rats,
pubmed-meshheading:9764821-Repressor Proteins,
pubmed-meshheading:9764821-Sequence Alignment,
pubmed-meshheading:9764821-Sequence Analysis, DNA,
pubmed-meshheading:9764821-Transcription Factors,
pubmed-meshheading:9764821-Vertebrates
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pubmed:year |
1998
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pubmed:articleTitle |
The C. elegans MDL-1 and MXL-1 proteins can functionally substitute for vertebrate MAD and MAX.
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pubmed:affiliation |
Department of Molecular Biology, Princeton University, New Jersey 08544-1014, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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