A novel expression vector composed of a regulatory element of the human leukosialin-encoding gene in different types of mammalian cells. NLM AIDSLINE Important note: Information in this article was accurate in 1995. The state of the art may have changed since the publication date.

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A novel expression vector composed of a regulatory element of the human leukosialin-encoding gene in different types of mammalian cells.

Gene. 1995 Jul 28;160(2):283-6. Unique Identifier : AIDSLINE MED/95369705
Xu A; Kudo S; Fukuda M; Alliance Pharmaceutical Corp., San Diego, CA 92121, USA.


Abstract: The regulatory element (RE) of the human leukosialin (LS)-encoding gene, that encodes a major sialoglycoprotein of human leukocyte and platelet membranes, was used to develop a novel expression vector, pKX. The vector was constructed by cloning a RE fragment and the SV40 fragment containing polyadenylation and splicing signals between HindIII and BamHI sites of the pCAT-Basic vector. The transcription level controlled by this vector was evaluated in six different cell lines using a transient expression assay of chloramphenicol acetyltransferase (CAT). The CAT activity of the pKX vector was compared to the other common expression vectors, namely pMSG (driven by the mouse mammary tumor virus LTR), pcDL-SR alpha (SV40 promoter/enhancer and HTLV-I LTR), pcDNAI (cytomegalovirus promoter/enhancer) and pCAT-Control (SV40 promoter/enhancer). The level of expression provided by the pKX vector was comparable to that observed with pcDNAI and pcDL-SR alpha vectors. In different mammalian cell lines, the highest efficiency of expression of the pKX vector was observed in the human T-cell lines, Jurkat and CEM, although the expression of pcDL-SR alpha-CAT in those cell lines was in the same range. The expression of the pKX vector driven by a non-viral promoter and/or enhancer can be as efficient as that driven by a viral promoter and/or enhancer. Potential uses of this vector may be found in studies of transient gene expression in hematopoietic cells and for gene therapy, particularly the ones involving T-cells.
Keywords: Animal Base Sequence Cells, Cultured Chloramphenicol Acetyltransferase/GENETICS Cloning, Molecular/*METHODS Comparative Study Cytomegalovirus/GENETICS Enhancer Elements (Genetics) Gene Therapy Genes, Reporter Genetic Vectors/*GENETICS Human HTLV-I/GENETICS Leukemia, T-Cell, Acute/PATHOLOGY Mammals Mammary Tumor Viruses, Mouse/GENETICS Molecular Sequence Data Organ Specificity Polyomavirus macacae/GENETICS Promoter Regions (Genetics)/*GENETICS *Regulatory Sequences, Nucleic Acid Repetitive Sequences, Nucleic Acid Sialoglycoproteins/*GENETICS Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. T-Lymphocytes/METABOLISM Transcription, Genetic Tumor Cells, Cultured JOURNAL ARTICLE

KWDanimalbasesequencecells,culturedchloramphenicolacetyltransferase/geneticscloning,molecular/KWDmethodscomparativestudycytomegalovirus/geneticsenhancerelements(genetics)genetherapygenes,reportergeneticvectors/KWDgeneticshumanhtlv-i/geneticsleukemia,t-cell,acute/pathologymammalsmammarytumorviruses,mouse/geneticsmolecularsequencedataorganspecificitypolyomavirusmacacae/geneticspromoterregions(genetics)/KWDgeneticsKWDregulatorysequences,nucleicacidrepetitivesequences,nucleicacidsialoglycoproteins/KWDgeneticssupport,non-uKWDsKWDgov'tsupport,uKWDsKWDgov't,pKWDhKWDsKWDt-lymphocytes/metabolismtranscription,genetictumorcells,culturedjournalarticle
951130
M95B0211


Copyright © 1995 - National Library of Medicine. Reproduced under license with the National Library of Medicine, Bethesda, MD.

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