US2014287475A1PendingUtilityA1

Methods For Eliminating Or Reducing The Expression Of A Gene In A Filamentous Fungal Strain

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Assignee: NOVOZYMES ASPriority: Dec 9, 2003Filed: Apr 17, 2014Published: Sep 25, 2014
Est. expiryDec 9, 2023(expired)· nominal 20-yr term from priority
C12N 2310/111C12N 2310/53C12N 2310/14C12N 15/1137C12N 15/113C12P 1/02
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Claims

Abstract

The present invention relates to methods for reducing or eliminating the expression of a target gene in a filamentous fungal strain, comprising: (a) inserting into the genome of the filamentous fungal strain a double-stranded transcribable nucleic acid construct comprising a first nucleotide sequence comprising a promoter operably linked to a homologous coding region of the target gene and a second nucleotide sequence comprising the homologous coding region, or a portion thereof, of the target gene, wherein the first and second nucleotide sequences are complementary to each other and the second nucleotide sequence is in reverse orientation relative to the first nucleotide sequence; and (b) inducing production of an interfering RNA encoded by the double-stranded transcribable nucleic acid construct by cultivating the filamentous fungal strain under conditions conducive for production of the interfering RNA; wherein the interfering RNA interacts with RNA transcripts of the target gene to reduce or eliminate expression of the target gene. The present invention also relates to the filamentous fungal strains and to methods of producing a biological substance of interest in such filamentous fungal strains.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for producing a biological substance, comprising:
 (a) cultivating an  Aspergillus niger , an  Aspergillus oryzae , or a  Trichoderma reesei  strain under conditions conducive for the production of the biological substance of interest, wherein the  Aspergillus niger , the  Aspergillus oryzae , or the  Trichoderma reesei  strain comprises a double-stranded transcribable nucleic acid construct comprising a first nucleotide sequence comprising a promoter operably linked to a first homologous transcribable region of a target gene encoding an undesirable biological substance and a second nucleotide sequence comprising a second homologous transcribable region of the target gene, wherein the first and second homologous regions are complementary to each other and the second homologous region is in reverse orientation relative to the first homologous region, wherein interfering RNA encoded by the double-stranded transcribable nucleic acid construct interacts with RNA transcripts of the target gene to reduce or eliminate expression of the target gene encoding the undesirable biological substance; and wherein the  Aspergillus niger , the  Aspergillus oryzae , or the  Trichoderma reesei  strain comprises a third nucleotide sequence encoding the biological substance of interest; and   (b) recovering the biological substance from the cultivation medium.   
     
     
         2 . The method of  claim 1 , wherein the first homologous region comprises at least 19 nucleotides of the target gene. 
     
     
         3 . The method of  claim 1 , wherein the second homologous region comprises at least 19 nucleotides of the first homologous region, wherein the least 19 nucleotides are in reverse order relative to the corresponding region of the first homologous region. 
     
     
         4 . The method of  claim 1 , wherein the first and second nucleotide sequences are separated by a fourth nucleotide sequence. 
     
     
         5 . The method of  claim 4 , wherein the fourth nucleotide sequence comprises at least 5 nucleotides. 
     
     
         6 . The method of  claim 1 , wherein expression of the target gene is reduced by at least 20%. 
     
     
         7 . The method of  claim 1 , wherein expression of the target gene is eliminated. 
     
     
         8 . The method of  claim 1 , wherein the interfering RNA interacts with RNA transcripts of one or more homologues of the target gene to reduce or eliminate expression of the one or more homologues of the target gene. 
     
     
         9 . The method of  claim 8 , wherein expression of the one or more homologues of the target gene is reduced by at least 20%. 
     
     
         10 . The method of  claim 9 , wherein expression of the one or more homologues of the target gene is eliminated.

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