Random-primed transcriptase in-vitro transcription method for rna amplification

Abstract

A random-primed reverse transcriptase-in vitro transcription method of linearly amplifying RNA is provided. According to the methods of the invention, source RNA (or other single-stranded nucleic acid), preferably, mRNA, is converted to double-stranded cDNA using two random primers, one of which comprises a RNA polymerase promoter sequence (“promoter-primer”), to yield a double-stranded cDNA that comprises a RNA polymerase promoter that is recognized by a RNA polymerase. Preferably, the primer for first-strand cDNA synthesis is a promoter-primer and the primer for second-strand cDNA synthesis is not a promoter-primer. The double-stranded cDNA is then transcribed into RNA by the RNA polymerase, optimally in the presence of a reverse transcriptase that is rendered incapable of RNA-dependent DNA polymerase activity during this transcription step. The subject methods produce linearly amplified RNA with little or no 3′ bias in the sequences of the nucleic acid population amplified.

1 . A method for amplifying one or more single stranded nucleic acids, said method comprising:
 (a) contacting said one or more single stranded nucleic acids with a first set of oligonucleotides, each of said oligonucleotides in said first set comprising a promoter sequence and a sequence from a set of random sequences of at least 4 nucleotides, a second set of oligonucleotides, each of said oligonucleotides in said second set comprising one of a set of random sequences of at least four nucleotides and one or more enzymes that alone or in combination catalyze the synthesis of double-stranded cDNA, under-conditions suitable for the production of double-stranded cDNA; and   (b) contacting the double-stranded cDNA produced in, step (a) with a RNA polymerase that recognizes said promoter sequence and ribonucleotides under conditions suitable to effect transcription, thereby producing sense or antisense RNA copies corresponding to said one or more single stranded nucleic acids.   
     
     
         2 . The method of  claim 1 , wherein the one or more single stranded nucleic acids are poly-A+ RNA. 
     
     
         3 . The method of  claim 1 , wherein the one or more enzymes is a reverse transcriptase. 
     
     
         4 . The method of  claim 3 , wherein the reverse transcriptase is rendered incapable of RNA-dependent DNA polymerase activity during the transcription step. 
     
     
         5 . The method of  claim 4 , wherein prior to step (b) said reverse transcriptase is inactivated. 
     
     
         6 - 7 . (canceled) 
     
     
         8 . The method of  claim 1 , wherein the random sequences of the oligonucleotides in said first set are 6 to 9 nucleotides. 
     
     
         9 . The method of  claim 1 , wherein the random sequences of the oligonucleotides in said second set are 6 to 9 nucleotides. 
     
     
         10 . The method of  claim 1 , wherein the random sequences of the oligonucleotides in said first set are 9 nucleotides. 
     
     
         11 . The method of  claim 1 , wherein the random sequences of the oligonucleotides in said second set are 6 nucleotides. 
     
     
         12 . The method of  claim 1 , wherein the oligonucleotides in said second set do not comprise a promoter sequence. 
     
     
         13 . (canceled) 
     
     
         14 . The method of  claim 1 , wherein step (a) further comprises contacting said one or more single-stranded nucleic acids with a third set of oligonucleotides each of said oligonucleotides of said third set comprising the promoter sequence and a polydT sequence of at least 5 nucleotides. 
     
     
         15 . The method of  claim 14 , wherein said polydT sequence is 5 to 25 nucleotides. 
     
     
         16 . The method of  claim 15 , wherein said polydT sequence is 18 nucleotides. 
     
     
         17 . The method of  claim 1 , wherein the promoter sequence is a T7 RNA polymerase promoter sequence and the RNA polymerase is T7 RNA polymerase. 
     
     
         18 . The method of  claim 1 , wherein the ribonucleotides comprise 5-(3-Aminoallyl)uridine 5′-triphosphate. 
     
     
         19 . The method of  claim 1 , wherein the sense or antisense RNA copies are labeled with Cy-NHS. 
     
     
         20 . The method of  claim 19 , wherein the Cy-NHS is Cy3-NHS or Cy5-NHS. 
     
     
         21 . A kit for use in amplifying single stranded nucleic acids into sense or antisense RNA, said kit comprising in one or more containers a first set of oligonucleotides, each of said oligonucleotides in said first set comprising a promoter sequence and one of a set of random sequences of at least 4 nucleotides; and a -second set of oligonucleotides, each of said oligonucleotides in said second set comprising one of a set of random sequences of at least four nucleotides. 
     
     
         22 . The kit of  claim 21 , which further comprises a reverse transcriptase and a RNA polymerase that recognizes said promoter sequence. 
     
     
         23 - 31 . (canceled) 
     
     
         32 . A method for amplifying one or more single stranded nucleic acids, said method comprising:
 (a) contacting said one or more single stranded nucleic acids with a first set of oligonucleotides, each of said oligonucleotides in said first set comprising a promoter sequence and a sequence from a set of random sequences of at least 4 nucleotides, and one or more enzymes that catalyze the synthesis of first strand cDNA, under conditions suitable for the production of first strand cDNA;   (b) contacting the first strand cDNA produced In step (a) with a second set of oligonucleotides, each of said oligonucleotides in said second set comprising one of a set of random sequences of at least four nucleotides and one or more enzymes that catalyze the synthesis of double-stranded cDNA, under conditions suitable for the production of double-stranded cDNA; and   (c) contacting the double-stranded cDNA produced in step (b) with a RNA polymerase that recognizes said promoter sequence-and ribonucleotides under conditions suitable to effect transcription, thereby producing sense or antisense RNA copies corresponding to said one or more single stranded nucleic acids.