Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2001-3-12
pubmed:abstractText
Inherited mutations of the TFIIH helicase subunits xeroderma pigmentosum (XP) B or XPD yield overlapping DNA repair and transcription syndromes. The high risk of cancer in these patients is not fully explained by the repair defect. The transcription defect is subtle and has proven more difficult to evaluate. Here, XPB and XPD mutations are shown to block transcription activation by the FUSE Binding Protein (FBP), a regulator of c-myc expression, and repression by the FBP Interacting Repressor (FIR). Through TFIIH, FBP facilitates transcription until promoter escape, whereas after initiation, FIR uses TFIIH to delay promoter escape. Mutations in TFIIH that impair regulation by FBP and FIR affect proper regulation of c-myc expression and have implications in the development of malignancy.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DNA Helicases, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/FUBP1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Green Fluorescent Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Luminescent Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-myc, http://linkedlifedata.com/resource/pubmed/chemical/RNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Repressor Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factor TFIIH, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, TFII, http://linkedlifedata.com/resource/pubmed/chemical/XPBC-ERCC-3 protein, http://linkedlifedata.com/resource/pubmed/chemical/poly-U binding splicing factor 60KDa
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0092-8674
pubmed:author
pubmed:issnType
Print
pubmed:day
9
pubmed:volume
104
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
353-63
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:11239393-Blotting, Western, pubmed-meshheading:11239393-Cell Line, pubmed-meshheading:11239393-DNA Helicases, pubmed-meshheading:11239393-DNA Repair, pubmed-meshheading:11239393-DNA-Binding Proteins, pubmed-meshheading:11239393-Enzyme Activation, pubmed-meshheading:11239393-Fibroblasts, pubmed-meshheading:11239393-Fluorescent Antibody Technique, pubmed-meshheading:11239393-Genes, Dominant, pubmed-meshheading:11239393-Green Fluorescent Proteins, pubmed-meshheading:11239393-Humans, pubmed-meshheading:11239393-Luminescent Proteins, pubmed-meshheading:11239393-Mutation, pubmed-meshheading:11239393-Neoplasms, pubmed-meshheading:11239393-Plasmids, pubmed-meshheading:11239393-Promoter Regions, Genetic, pubmed-meshheading:11239393-Protein Binding, pubmed-meshheading:11239393-Protein Structure, Tertiary, pubmed-meshheading:11239393-Proto-Oncogene Proteins c-myc, pubmed-meshheading:11239393-RNA-Binding Proteins, pubmed-meshheading:11239393-Recombinant Proteins, pubmed-meshheading:11239393-Repressor Proteins, pubmed-meshheading:11239393-Transcription, Genetic, pubmed-meshheading:11239393-Transcription Factor TFIIH, pubmed-meshheading:11239393-Transcription Factors, pubmed-meshheading:11239393-Transcription Factors, TFII, pubmed-meshheading:11239393-Transfection, pubmed-meshheading:11239393-Xeroderma Pigmentosum
pubmed:year
2001
pubmed:articleTitle
Defective interplay of activators and repressors with TFIH in xeroderma pigmentosum.
pubmed:affiliation
Gene Regulation Section, Laboratory of Pathology, National Cancer Institute, National Institute of Health, Bethesda, MD 20892, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't