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filingDate 1990-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1993-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_58bcf133fcc0647b7818fab94035398f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4791fe12d20a7323e0d56a23753728f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ffe8e4b45abc12d6bd3d3993af156dd5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bda23d2df408757b70bc768c4d642787
publicationDate 1993-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5215910-A
titleOfInvention Host cells transformed with sterol regulatory elements
abstract Disclosed are discreet functionally translocatable DNA segments, termed Sterol Regulatory Elements (SRE's), which are fused to heterologous structural genes to provide sterol regulatory capability to the thus formed hybrid gene. The hybrid genes respond to sterols by decreasing the production of messenger RNA. The SRE segments contain as their primary functional nucleotide sequence, a 16 bp sequence referred to as direct repeat 2, isolated from the 5' regions of the human LDL receptor gene. DNA segments which include this 16 nucleotide long sequence similarly confer sterol regulatory capability to previously known promoters such as the HSV TK promoter. Also disclosed are discreet sequences which confer positive transcription promotion to heterologous structural genes and promoters without conferring sterol responsivity. Methods are disclosed for employing these genetic control elements in a myriad of embodiments which provide for a fine-tune control of heterologous genes. Methods are also disclosed for employing the SRE in a screening assay for drugs capable of stimulating the cell to synthesize LDL receptors.
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priorityDate 1987-03-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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