NDLI: Transduction of human colony-stimulating factor-1 (CSF-1) receptor into interleukin-3-dependent mouse myeloid cells induces both CSF-1-dependent and factor-independent growth.

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Development of an in vitro transcription system for Neurospora crassa mitochondrial DNA and identification of transcription initiation sites.

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Characterization of a conserved extrachromosomal element isolated from the avian malarial parasite Plasmodium gallinaceum.

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Three light-inducible heat shock genes of Chlamydomonas reinhardtii.

In vivo construction of linear vectors based on killer plasmids from Kluyveromyces lactis: selection of a nuclear gene results in attachment of telomeres.

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High incidence of lung, bone, and lymphoid tumors in transgenic mice overexpressing mutant alleles of the p53 oncogene.

Regulation of STA1 gene expression by MAT during the life cycle of Saccharomyces cerevisiae.

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Homologous plasmid recombination is elevated in immortally transformed cells.

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Effect of silencer on polyomavirus DNA replication.

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Isolation and characterization of three distinct cDNAs for the chicken c-ski gene.

Cloning and disruption of Ustilago maydis genes.

A large internal deletion converts yeast LEU3 to a constitutive transcriptional activator.

A lysine substitution in the ATP-binding site of eucaryotic initiation factor 4A abrogates nucleotide-binding activity.

Conservation of function and regulation within the Cdc28/cdc2 protein kinase family: characterization of the human Cdc2Hs protein kinase in Saccharomyces cerevisiae.

Transduction of human colony-stimulating factor-1 (CSF-1) receptor into interleukin-3-dependent mouse myeloid cells induces both CSF-1-dependent and factor-independent growth.

DNA determinants of structural and regulatory variation within the murine beta-glucuronidase gene complex.

The mouse thymidylate synthase promoter: essential elements are in close proximity to the transcriptional initiation sites.

Substitution of lysine for arginine at position 42 of human transforming growth factor-alpha eliminates biological activity without changing internal disulfide bonds.

Transforming mutant v-mos protein kinases that are deficient in in vitro autophosphorylation.

The CUP2 gene product, regulator of yeast metallothionein expression, is a copper-activated DNA-binding protein.

Integration of an aberrant retrotransposon in Saccharomyces cerevisiae.

Transcription factor Sp1 binds to and activates a human hsp70 gene promoter.

Calcium phosphate-mediated transfection alters metallothionein gene expression in response to Cd2+ and Zn2+.

Autoregulation of interleukin 6 and granulocyte-macrophage colony-stimulating factor in the differentiation of myeloid leukemic cells.

Isolation of a gene that down-regulates nitrate assimilation and influences another regulatory gene in the same system.

Functional Domains of the Drosophila melanogaster Muscle Myosin Heavy-Chain Gene Are Encoded by Alternatively Spliced Exons

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Transduction of human colony-stimulating factor-1 (CSF-1) receptor into interleukin-3-dependent mouse myeloid cells induces both CSF-1-dependent and factor-independent growth.

Content Provider	PubMed Central
Author	Kato, J. Y. Roussel, M. F. Ashmun, R. A. Sherr, C. J.
Abstract	A retroviral vector encoding the receptor for human colony-stimulating factor-1 (CSF-1) was introduced into murine myeloid FDC-P1 cells which require interleukin-3 (IL-3) for their proliferation and survival in culture. Cells expressing the CSF-1 receptor (CSF-1R), selected by fluorescence-activated cell sorting in the continued presence of murine IL-3, formed colonies in semisolid medium and were able to proliferate continuously in liquid cultures containing human recombinant CSF-1. Thus, although they do not synthesize endogenous murine CSF-1R, FDC-P1 cells express the downstream components of the CSF-1 mitogenic pathway necessary for its signal-response coupling. After receptor transduction, slowly proliferating factor-independent variants that produced neither CSF-1 nor growth factors able to support the proliferation of parental FDC-P1 cells also arose. When the human CSF-1R was expressed in FDC-P1 cells under the control of an inducible metallothionein promoter, the frequencies of both CSF-1-responsive and factor-independent variants increased after heavy-metal treatment. In addition, a monoclonal antibody to human CSF-1R arrested colony formation by both the CSF-1-dependent and factor-independent cells but did not affect their growth in response to IL-3. Therefore, the induction of both the CSF-1-dependent and factor-independent phenotypes depended on expression of the transduced human CSF-1R.
Starting Page	4069
File Format	PDF
ISSN	10985549
e-ISSN	10985549
Journal	Molecular and Cellular Biology
Issue Number	9
Volume Number	9
Language	English
Publisher Date	1989-09-01
Access Restriction	Open
Subject Keyword	Research in Higher Education
Content Type	Text
Resource Type	Article
Subject	Cell Biology Molecular Biology

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