FUNCTIONAL NUCLEIC ACIDS AND METHODS

• US 20100087336A1
• Filed: 09/12/2009
• Published: 04/08/2010
• Est. Priority Date: 03/08/2007
• Status: Abandoned Application

• Current Assignee: BioTex Incorporated, University of Houston (University of Houston System)
• Original Assignee: BioTex Incorporated, University of Houston (University of Houston System)
• Inventors: Strych, Ulrich, Fox, George E., Stepanov, Victor G., Liu, Yamei, Jackson, George, McNichols, Roger
• Application Number:
  US12/558,523
• Publication Number:
  US 20100087336A1
• Time in Patent Office: Days
• US Class Current: 506/26
• CPC Class Codes: G01N 33/5308 for analytes not provided for elsewhere, e.g. nucleic acids, uric acid, worms, mites

Abstract

The present invention relates to methods of generating amounts of selective nucleic acids. The present invention further relates to selective nucleic acids incorporated within non-coding nucleic acids, capable of binding to or altering a target molecule. Selective nucleic acids may generally refer to, but are not limited to, deoxyribonucleic acids (DNAs), ribonucleic acids (RNAs), artificially modified nucleic acids, combinations or modifications thereof. Selective nucleic acids may also generally refer to, but are not limited to, nucleic acid aptamers, aptazymes, ribozymes, deoxyribozymes, nucleic acid probes, small interfering RNAs (siRNAs), micro RNAs (miRNAs), short hairpin RNAs (shRNAs), antisense nucleic acids, diagnostic probes or probe libraries, aptamer inhibitors, precursors of any of the above and/or combinations or modifications thereof. In one aspect, a method for generating amounts of selective nucleic acids includes incorporating a selective nucleic acid sequence into a carrier nucleic acid. In general, the carrier nucleic acid may be transcribed by a cell into a product nucleic acid which may carry an incorporated selective nucleic acid sequence.

Claims

1. An expression vector comprising:

a chimeric gene encoding a gene product comprising a selective nucleic acid within a carrier nucleic acid, wherein said selective nucleic acid is capable of binding to or affecting at least one target molecule;

wherein said expression vector when transfected into a host transcribes said chimeric gene.

2. The expression vector of claim 1, wherein said vector further comprises at least one of a functional promoter, a selection marker or a marker for selective induction.

3. The expression vector of claim 2, wherein said at least one selection marker comprises an antibiotic resistance marker.

4. The expression vector of claim 2, wherein said promoter is a T7 RNA polymerase or a ribosomal RNA promoter.

5. The expression vector of claim 1, wherein said selective nucleic acid comprises at least one of a short interfering RNA (siRNA);

a micro RNA (miRNA);

a short hairpin RNA (shRNA);

an aptamer;

a ribozyme;

an aptazyme;

a riboswitch;

an aptamer inhibitor;

an antisense nucleic acid;

a probe library, a diagnostic probe;

a precursor thereof or a combination thereof.

6. The expression vector of claim 1, wherein said carrier nucleic acid is selected from the group consisting of rRNA, tRNA, RNAase P, small nuclear RNA (snRNA), small nucleolar RNA (snoRNA), efference RNA (eRNA) and tmRNA.

7. The expression vector of claim 1, wherein said at least one target molecule is a nucleic acid.

8. The expression vector of claim 7, wherein said nucleic acid is a messenger RNA (mRNA).

9. The expression vector of claim 8, wherein said selective nucleic acid participates in an RNA interference (RNAi) mechanism.

10. The expression vector of claim 1, further comprising at least one self-excising RNAzyme sequence.

11. The expression vector of claim 1, further comprising at least a sequence complementary to the hybridization sequence of a DNAzyme.

12. An isolated cell comprising:

at least one selective nucleic acid sequence incorporated into a genomic DNA encoding a non-coding nucleic acid, wherein said selective nucleic acid binds to or affects a target molecule.

13. The cell of claim 12, wherein said selective nucleic acid is incorporated into said non-coding nucleic acid by homologous recombination.

14. The cell of claim 12, wherein said non-coding nucleic acid is selected from the group consisting of rRNA, tRNA, RNAase P, small nuclear RNA (snRNA), small nucleolar RNA (snoRNA), efference RNA (eRNA) and tmRNA.

15. The cell of claim 12, wherein said cell is a prokaryotic cell or a eukaryotic cell.

16. The cell of claim 12, wherein said selective nucleic acid comprises at least one of a short interfering RNA (siRNA);

a micro RNA (miRNA);

a short hairpin RNA (snRNA);

an aptamer;

a ribozyme;

an aptazyme;

a riboswitch;

an aptamer inhibitor;

an antisense nucleic acid;

a probe library, a diagnostic probe;

a precursor thereof or a combination thereof.

17. The cell of claim 12, wherein said at least one target molecule is a nucleic acid.

18. The cell of claim 17, wherein said nucleic acid is an mRNA.

19. The cell of claim 12, wherein said selective nucleic acid participates in an RNAi mechanism.

20. A method for generating amounts of selective nucleic acids comprising:

generating a library of nucleic acid sequences encoding selective nucleic acid capable of binding to or affecting at least one target molecule;

incorporating said nucleic acid sequences in at least one carrier nucleic acid in a cell;

culturing said cell to achieve a cell population; and

purifying selective nucleic acids incorporated into carrier nucleic acids from said cell population.

21. The method of claim 20, wherein said cell is selected from the group consisting of E. coli, Staphylococcus, Bacillus, Pseudomonas, Citrobacteia, Klebsilla, and Rhodococcus or Saccharomyces (yeast).

22. The method of claim 20, wherein purifying said selective nucleic acids incorporated into carrier nucleic acids comprises at least partially lysing cells of said cell population and at least partially selectively purifying nucleic acids of a certain size range.

23. The method of claim 22, further comprising excising said selective nucleic acids from said carrier nucleic acids.

24. The method of claim 23, wherein said excising comprises using RNases, DNAzymes, chemical scissors or a combination thereof.

25. The method of claim 21, wherein said cell is selected or modified for deficient or inducible activity of at least one RNase.