Highly efficient dual T7/T3 promoter vector PJKF16 and dual SP6/T3 promoter vector PJFK15

Claim 2

A dual phage RNA polymerase promoter vector having a polylinker with a multiple cloning site, which polylinker is linked at one of its ends to a T3 phage RNA polymerase promoter, which has a consensus sequence recognized specifically by a recombinant-synthesized T3 polymerase and on the other of its ends, to a second phage RNA polymerase promoter, other than the T3 RNA polymerase promoter, the T3 promoter being capable of initiating efficient transcription of DNA at a concentration of ribonucleoside triphosphates of 10 micromolar or less, wherein said promoter does not contain a thymidine residue in the first ten nucleotides downstream of the initiation site, wherein transcription from either of the phage promoters proceeds toward the other promoter and in a direction opposite from the direction of transcription of the other phage promoter and the phage polymerase capable of transcription from said promoters is specific and does not recognize the other phage promoter.

Claim 3

The dual RNA polymerase promoter vector of claim 1 wherein the second promoter is selected from the group consisting of phage RNA polymerase promoters phage T7 and SP6.

Claim 4

The dual RNA polymerase promoter vector of claim 2 wherein the second promoter is a RNA polymerase promoter.

Claim 5

The dual phage RNA polymerase promoter vector of claim 1 wherein the consensus sequence is contained in a nucleotide sequence selected from the group of sequences consisting of AATTCGTCTCTCCCTTTAGTGAGGGTT and AATTAACCCTCACTAAAGGGAGAGACG.

Claim 6

The dual phage RNA polymerase promoter vector of claim 4 wherein the sequence is AATTAQACCCTCACTAAAGGGAGAGACG.

Claim 7

The dual phage RNA polymerase promoter vector of claim 1 wherein the concentration of a ribonucleoside triphosphate necessary for efficient transcription is less than 10 micromolar.

Claim 8

A recombinant DNA vector which comprises a polylinker sequence having linked to one of its ends a T3 phage RNA polymerase promoter which has a consensus sequence recognized specifically by a recombinant-synthesized T3 polymerase and at the other of its ends, a second phage RNA polymerase promoter, wherein said second promoter is a promoter other than a T3 phage RNA polymerase promoter and a DNA sequence inserted in the polylinker sequence, the respective promoters being in opposite orientation, the recombinant DNA vector being capable of transcription of DNA to produce RNA strands complementary to either one of the strands of the inserted DNA sequence when there is supplied to the vector a phage promoter-specific polymerase, the T3 promoter being capable of initiating efficient transcription of DNA at low concentrations of ribonucleoside triphosphates of 10 micromolar or less, wherein said promoter does not contain a thymidine residue in the first ten nucleotides downstream of the initiation site, wherein transcription from either of the phage promoters proceeds toward the other promoter and in a direction opposite from the direction of transcription of the other phage promoter and the phage polymerase capable of transcription from said promoters is specific and does not recognize the other phage promoter.

Claim 9

A recombinant DNA vector which comprises a polylinker sequence having linked to one of its ends a T3 phage RNA polymerase promoter which has a consensus sequence recognized specifically by a recombinant-synthesized T3 polymerase and at the other of its ends, a second phage RNA polymerase promoter, wherein said second promoter is a promoter other than a T3 phage RNA polymerase promoter and a DNA sequence inserted in the polylinker sequence, the respective promoters being in opposite orientation, the recombinant DNA vector being capable of transcription of DNA to produce RNA strands complementary to either one of the strands of the inserted DNA sequence when there is supplied to the vector a phage promoter-specific polymerase, the T3 promoter being capable of initiating efficient transcription of DNA at low concentrations of ribonucleoside triphosphates of 10 micromolar or less, wherein said promoter does not contain a thymidine residue in the first ten nucleotides downstream of the initiation site, wherein transcription from either of the phage promoters proceeds toward the other promoter and in a direction opposite from the direction of transcription of the other phage promoter and the phage polymerase capable of transcription from said promoters is specific and does not recognize the other phage promoter.

Claim 10

The recombinant DNA vector of claim 7 wherein the second promoter is a T7 RNA polymerase promoter.

Claim 11

The recombinant DNA vector of claim 7 which lacks restriction sites for enzymes SphI and BglII, whereby the vector is resistant to cleavage by these two enzymes.

Claim 12

The recombinant DNA vector of claim 7 wherein the consensus sequence is contained in a nucleotide sequence selected from the group of sequences consisting of: AATTCGTCTCTCCCTTTAGTGAGGGTT and AATTAACCCTCACTAAAGGGAGAGACG.

Claim 13

The recombinant DNA vector of claim 10 wherein the sequence is AATTAACCCTCACTAAAGGGAGAGACG.

Claim 14

The recombinant DNA vector of claim 7 wherein the concentration of a ribonucleoside triphosphate necessary for efficient transcription is less than 10 micromolar.

Claim 15

A kit for genetic applications especially for transcription of DNA to synthesize RNA transcripts complementary to either strand of a DNA sequence, which kit comprises in combination the following components: a recombinant-synthesized T3 RNA polymerase, a recombinant-synthesized T7 RNA polymerase and a dual promoter transcription vector having a T3 phage RNA promoter for said T3 polymerase and a T7 phage RNA promoter for said T7 polymerase, the respective promoters being linked at opposite ends of the polylinker and in opposite orientation, said T3 having a consensus sequence recognized by T3 polymerase, wherein the first ten nucleotides downstream of the initiation site do not contain a thymidine residue, with which kit, components and cleaved vector, RNA transcripts can be synthesized that are complementary to either one of the strands of cloned DNA sequence, the T3 promoter being capable of efficient transcription of DNA at low concentrations of ribonucleoside triphosphates of 10 micromolar or less, wherein transcription from either of the phage promoters proceeds toward the other promoter and in a direction opposite from the direction of transcription of the other phage promoter and the phage polymerase capable of transcription from said promoters is specific and does not recognize the other phage promoter.

Claim 16

A kit for genetic applications especially for transcription of DNA to synthesize RNA transcripts complementary to either strand of a DNA sequence, which kit comprises in combination the following components: a recombinant-synthesized T3 RNA polymerase, a recombinant-synthesized T7 RNA polymerase and a dual promoter transcription vector having a T3 phage RNA promoter for said T3 polymerase and a T7 phage RNA promoter for said T7 polymerase, the respective promoters being linked at opposite ends of the polylinker and in opposite orientation, said T3 having a consensus sequence recognized by T3 polymerase, wherein the first ten nucleotides downstream of the initiation site do not contain a thymidine residue, with which kit, components and cleaved vector, RNA transcripts can be synthesized that are complementary to either one of the strands of cloned DNA sequence, the T3 promoter being capable of efficient transcription of DNA at low concentrations of ribonucleoside triphosphates of 10 micromolar or less, wherein transcription from either of the phage promoters proceeds toward the other promoter and in a direction opposite from the direction of transcription of the other phage promoter and the phage polymerase capable of transcription from said promoters is specific and does not recognize the other phage promoter.

Claim 17

The kit of claim 13 wherein the concentration of a ribonucleoside triphosphate necessary for efficient transcription in less than 10 micromolar.