Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1994-3-28
pubmed:databankReference
pubmed:abstractText
The expression of a membrane-associated folate receptor (FR) was elevated in spleen samples from patients with chronic (CML) and acute (AML) myelogenous leukemias compared with normal spleen. Contrary to earlier reports, antibodies to a purified FR from placenta cross-reacted quantitatively with this protein in solution radioimmunoassays. Similar to FR-alpha (KB cells) and FR-beta (placenta), the protein was released from the membrane by phosphatidylinositol-specific phospholipase C, indicating a glycosylphosphatidylinositol (GPI) membrane anchor. Screening of a cDNA library from CML spleen with a heterologous murine FR cDNA and also amplification of FR cDNAs from spleen and bone marrow in CML, AML, chronic lymphocytic leukemia (CLL), and acute lymphocytic leukemia (ALL) by polymerase chain reaction (PCR) using degenerate oligonucleotides yielded cDNA clones representing FR-beta, a novel FR (type gamma), and an aberrant transcript of FR-gamma with a 2 base pair deletion resulting in a truncated 104-residue polypeptide; FR-alpha was not detected in these tissues. The cDNA for FR-gamma predicts a 243-residue polypeptide with an amino acid sequence homology of 71% and 79% with FR-alpha and FR-beta, respectively, a 23-residue amino-terminal signal peptide, and 3 potential sites for N-linked glycosylation. Transfection of COS-1 cells with the cDNA for FR-gamma resulted in low expression of a [3H]folic acid binding protein on the cell surface that was GPI-anchored. PCR analysis of total RNA from a number of normal and malignant tissues and cell lines indicated a limited tissue specificity of FR-gamma.(ABSTRACT TRUNCATED AT 250 WORDS)
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
0006-2960
pubmed:author
pubmed:issnType
Print
pubmed:day
8
pubmed:volume
33
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1209-15
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:8110752-Amino Acid Sequence, pubmed-meshheading:8110752-Animals, pubmed-meshheading:8110752-Base Sequence, pubmed-meshheading:8110752-Bone Marrow, pubmed-meshheading:8110752-Bone Marrow Cells, pubmed-meshheading:8110752-Carrier Proteins, pubmed-meshheading:8110752-Cell Membrane, pubmed-meshheading:8110752-Cloning, Molecular, pubmed-meshheading:8110752-DNA, Complementary, pubmed-meshheading:8110752-Folate Receptors, GPI-Anchored, pubmed-meshheading:8110752-Hematopoietic Stem Cells, pubmed-meshheading:8110752-Humans, pubmed-meshheading:8110752-Leukemia, Myelogenous, Chronic, BCR-ABL Positive, pubmed-meshheading:8110752-Leukemia, Myeloid, Acute, pubmed-meshheading:8110752-Mice, pubmed-meshheading:8110752-Molecular Sequence Data, pubmed-meshheading:8110752-Receptors, Cell Surface, pubmed-meshheading:8110752-Sequence Homology, Amino Acid, pubmed-meshheading:8110752-Spleen
pubmed:year
1994
pubmed:articleTitle
Identification of a novel folate receptor, a truncated receptor, and receptor type beta in hematopoietic cells: cDNA cloning, expression, immunoreactivity, and tissue specificity.
pubmed:affiliation
Department of Biochemistry and Molecular Biology, Medical College of Ohio, Toledo 43614.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't