Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1992-3-12
pubmed:abstractText
HSB-2 is a cell line derived from a patient who had T-cell acute lymphoblastic leukemia (T-cell ALL) with a t(1;7)(p34;q34). We used a genomic probe from the T-cell receptor beta (TCR beta) locus (7q34) to identify DNA rearrangements in HSB-2. Two rearranged BglII DNA fragments were cloned, and one of these clones was shown to contain the translocation breakpoint on the derivative chromosome I [der(I)]. We used a probe derived from this clone to isolate an unrearranged phage clone encompassing the breakpoint at Ip34. The restriction map of this clone was compared to the published maps of known protooncogenes located at Ip32-34. By restriction mapping, Southern blot analysis, and DNA sequencing we showed that the translocation breakpoint on chromosome I is located within the first intron of the LCK gene. The LCK gene codes for p56lck, a member of the SRC family of cytoplasmic tyrosine protein kinases. There are two classes of LCK transcripts (type I and type II), each expressed from a distinct promoter, and each having a unique 5' untranslated region (UTR); the protein coding regions of the two classes are identical. The breakpoint in the t(1;7) separates the two LCK promoters and juxtaposes the constant region of the TCR beta locus with the proximal promoter and with the protein-coding region of the LCK gene on the der(I) chromosome.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1045-2257
pubmed:author
pubmed:issnType
Print
pubmed:volume
3
pubmed:geneSymbol
TAL1
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
461-7
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:1663780-Base Sequence, pubmed-meshheading:1663780-Chromosomes, Human, Pair 1, pubmed-meshheading:1663780-Chromosomes, Human, Pair 7, pubmed-meshheading:1663780-DNA Probes, pubmed-meshheading:1663780-Gene Expression Regulation, Leukemic, pubmed-meshheading:1663780-Gene Rearrangement, beta-Chain T-Cell Antigen Receptor, pubmed-meshheading:1663780-Genetic Markers, pubmed-meshheading:1663780-Humans, pubmed-meshheading:1663780-Leukemia-Lymphoma, Adult T-Cell, pubmed-meshheading:1663780-Lymphocyte Specific Protein Tyrosine Kinase p56(lck), pubmed-meshheading:1663780-Molecular Sequence Data, pubmed-meshheading:1663780-Neoplasm Proteins, pubmed-meshheading:1663780-Oncogenes, pubmed-meshheading:1663780-Promoter Regions, Genetic, pubmed-meshheading:1663780-Proto-Oncogene Proteins, pubmed-meshheading:1663780-RNA, Messenger, pubmed-meshheading:1663780-RNA, Neoplasm, pubmed-meshheading:1663780-Receptors, Antigen, T-Cell, alpha-beta, pubmed-meshheading:1663780-Translocation, Genetic, pubmed-meshheading:1663780-Tumor Cells, Cultured, pubmed-meshheading:1663780-Tumor Markers, Biological
pubmed:year
1991
pubmed:articleTitle
The LCK gene is involved in the t(1;7)(p34;q34) in the T-cell acute lymphoblastic leukemia derived cell line, HSB-2.
pubmed:affiliation
Department of Medicine, University of Chicago, IL 60637.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't