US2003003543A1PendingUtilityA1
Methods and applications for efficient genetic suppressor elements
Priority: Sep 7, 1993Filed: Apr 22, 2002Published: Jan 2, 2003
Est. expirySep 7, 2013(expired)· nominal 20-yr term from priority
C12N 15/63C12N 15/1051C12N 15/1082C12N 15/67C12Q 1/6811C40B 40/06C12N 15/1079C40B 40/08C12N 15/1072C40B 50/06
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Claims
Abstract
Methods for isolating and identifying genetic elements that are capable of inhibiting gene function are disclosed, as well as genetic elements isolated or identified according to the method of the invention and host cells modified by genetic modification using genetic suppressor elements according to the invention.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A synthetic peptide comprising a sense-oriented genetic suppressor element obtained by a method of obtaining genetic suppressor elements (GSEs) comprising the steps of:
(a) randomly fragmenting DNA homologous to a gene to be suppressed, to yield DNA fragments; (b) transferring the DNA fragments to an expression vector to yield a library, wherein the expression vector is capable of expressing the DNA fragments in a living cell in which gene suppression can be selected or screened; (c) genetically modifying living cells by introducing the genetic suppressor elements library into the living cells; (d) isolating or enriching for genetically modified living cells containing genetic suppressor elements by selecting or screening for gene suppression, and; (e) obtaining the genetic suppressor element from the genetically modified cells.
2 . A synthetic peptide having an amino acid sequence corresponding to the amino acid sequence encoded by a genetic suppressor element produced by a method comprising the steps of:
(a) obtaining genomic DNA or a total cDNA population from the cells; (b) randomly fragmenting the genomic DNA or total cDNA population to produce random DNA fragments; (c) ligating the random DNA fragments to synthetic adaptors to produce amplifiable random DNA fragments; (d) cloning the amplified mixture of random DNA fragments into a suitable expression vector having a selectable marker to produce a random fragment expression library; (e) transferring the random fragment expression library into appropriate the random fragment expression library into appropriate target cells; (f) selecting the target cells for the presence of the selectable marker present in the expression vector to obtain target cells having the selectable marker; (g) selecting or screening the target cells having the selectable marker for the selectable or screenable phenotype conferred upon the cells by inactivation of a recessive gene by a GSE; and (h) recovering the GSE from the target cell having the selectable or screenable phenotype.
3 . A synthetic peptide of claim 1 that suppresses Topoisomerase II activity.
4 . A synthetic peptide of claim 2 that suppresses Topoisomerase II activity.
5 . A synthetic peptide of claim 1 that suppresses β 2 -microglobulin activity
6 . A synthetic peptide of claim 2 that suppresses β 2 -microglobulin activity
7 . A synthetic peptide of claim 1 that suppresses MHC Class I protein activity.
8 . A synthetic peptide of claim 2 that suppresses MHC Class I protein activity.
9 . A synthetic peptide of claim 1 that suppresses HLA Class I protein activity.
10 . A synthetic peptide of claim 2 that suppresses HLA Class I protein activity.Join the waitlist — get patent alerts
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