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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
51
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pubmed:dateCreated |
1998-1-22
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pubmed:abstractText |
The human proto-oncogene c-myc encodes two proteins, c-Myc1 and c-Myc2, from two initiation codons, CUG and AUG, respectively. It is also transcribed from four alternative promoters (P0, P1, P2, and P3), giving rise to different RNA 5'-leader sequences, the long sizes of which suggest that they must be inefficiently translated by the classical ribosome scanning mechanism. Here we have examined the influence of three c-myc mRNA 5'-leaders on the translation of chimeric myc-CAT mRNAs. We observed that in the reticulocyte rabbit lysate, these 5'-leaders lead to cap-independent translation initiation. To determine whether this kind of initiation resulted from the presence of an internal ribosome entry site (IRES), COS-7 cells were transfected with bicistronic vectors containing the different c-myc 5'-leaders in the intercistronic region. An IRES was identified, requiring elements located within the P2 leader, between nucleotides -363 and -94 upstream from the CUG start codon. This is the first demonstration of the existence of IRES-dependent translation for a proto-oncogene. This IRES could be a translation enhancer, allowing activation of c-myc expression under the control of trans-acting factors and in response to specific cell stimuli.
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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/Chloramphenicol O-Acetyltransferase,
http://linkedlifedata.com/resource/pubmed/chemical/Codon,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/RNA Caps,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0021-9258
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
19
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pubmed:volume |
272
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
32061-6
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:9405401-Animals,
pubmed-meshheading:9405401-Base Sequence,
pubmed-meshheading:9405401-COS Cells,
pubmed-meshheading:9405401-Chloramphenicol O-Acetyltransferase,
pubmed-meshheading:9405401-Codon,
pubmed-meshheading:9405401-Genes, myc,
pubmed-meshheading:9405401-Humans,
pubmed-meshheading:9405401-Molecular Sequence Data,
pubmed-meshheading:9405401-Nucleic Acid Conformation,
pubmed-meshheading:9405401-Promoter Regions, Genetic,
pubmed-meshheading:9405401-Protein Biosynthesis,
pubmed-meshheading:9405401-RNA, Messenger,
pubmed-meshheading:9405401-RNA Caps,
pubmed-meshheading:9405401-Recombinant Fusion Proteins,
pubmed-meshheading:9405401-Ribosomes,
pubmed-meshheading:9405401-Sequence Homology, Nucleic Acid,
pubmed-meshheading:9405401-Tumor Cells, Cultured
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pubmed:year |
1997
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pubmed:articleTitle |
Alternative translation of the proto-oncogene c-myc by an internal ribosome entry site.
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pubmed:affiliation |
INSERM U397, Endocrinologie et Communication Cellulaire, Institut Louis Bugnard, Centre Hospitalier Universitaire Rangueil, Avenue Jean Poulhès, 31403 Toulouse Cedex 04, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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