Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
1994-1-3
pubmed:abstractText
L-type pyruvate kinase (L-PK) gene expression is modulated by hormonal and nutritional conditions. We have previously shown that the glucose/insulin response element (GlRE) of the L-PK gene is built around two noncanonical E boxes (element L4) that cooperate closely with a contiguous binding site (element L3). We present in this report the identification of proteins that interact with both elements. The L3 site binds hepatocyte nuclear factor 4 (HNF4)- and COUP/TF-related proteins. In fibroblasts, the overexpression of HNF4 transactivates the L-PK promoter. On the contrary, COUP/TF strongly inhibits the active promoter in hepatocytes. The L4 site binds the major late transcription factor (MLTF) in vitro and ex vivo; mutations that suppress this binding activity also inactivated the GlRE function. Mutations transforming one or two noncanonical E boxes of element L4 into consensus MLTF/USF binding sites strongly increase the affinity for MLTF/USF and do not impair the glucose responsiveness. However, merely the ability to bind MLTF/USF does not seem to be sufficient to confer a GlRE activity: those elements in which one E box has been destroyed and the other has been transformed into a consensus MLTF/USF sequence bind MLTF/USF efficiently but do not confer a high glucose responsiveness on the L-PK gene promoter. Consequently, the full activity of the L-PK GlRE seems to require the cooperation between two putative MLTF/USF binding sites located in the vicinity of an HNF4 binding site.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-1312668, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-1315961, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-1406667, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-1406684, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-1549130, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-1589769, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-1618827, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-1639815, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-1734282, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-1748280, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-1848696, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-1899293, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-2006410, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-2026584, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-2115126, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-2246264, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-2249772, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-2251503, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-2279702, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-2338243, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-2545675, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-2585483, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-2739739, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-3011791, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-3396073, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-3821727, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-4705382, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-6960240, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-8094701, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-8483904, http://linkedlifedata.com/resource/pubmed/commentcorrection/8246989-8509413
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0270-7306
pubmed:author
pubmed:issnType
Print
pubmed:volume
13
pubmed:geneSymbol
L-PK
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
7725-33
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed:year
1993
pubmed:articleTitle
Functional characterization of the L-type pyruvate kinase gene glucose response complex.
pubmed:affiliation
Laboratoire de Recherches en Génétique et Pathologie Moléculaire, Institut Cochin de Génétique Moléculaire, INSERM U-129, CHU Cochin, Paris, France.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't