Compositions and methods for preparing short RNA molecules and other nucleic acids

• US 20050054847A1
• Filed: 07/30/2004
• Published: 03/10/2005
• Est. Priority Date: 08/01/2003
• Status: Abandoned Application

• Current Assignee: Life Technologies Corporation (Thermo Fisher Scientific Incorporated)
• Original Assignee: Invitrogen Corp. (Thermo Fisher Scientific Incorporated)
• Inventors: Harris, Adam N., Madden, Knut R., Hecker, Karl H., Lee, Byung-in
• Application Number:
  US10/902,704
• Publication Number:
  US 20050054847A1
• Time in Patent Office: Days
• US Class Current: 536/25.400
• CPC Class Codes: B01D 15/3804 Affinity chromatography
• CPC Class Codes: C07H 21/02 with ribosyl as saccharide radical
• CPC Class Codes: C12N 15/111 General methods applicable to biologically active non-coding nucleic acids
• CPC Class Codes: C12N 2330/31 Libraries, arrays

Abstract

The invention provides methods of preparing nucleic acids, such as RNA molecules, of a defined size or range of sizes. The invention provides compositions, methods and kits for use in the production and preparation of small RNA molecules (including without limitation micro-RNA, siRNA, d-siRNA and e-siRNA) and other nucleic acids of various sizes.

Claims

1-62. -62. (Canceled).

63. A method for separating RNA molecules with a length of from about 10 to about 200 nucleotides from RNA molecules with a length greater than about 200 nucleotides, the method comprising:

(a) preparing a mixture comprising;

(i) a population of RNA molecules which vary in length; and

(ii) an alcohol;

(b) applying the mixture of (a) to an affinity column; and

(c) eluting RNA molecules which are retained on the column, wherein RNA molecules with a length from about 10 to about 200 nucleotides are retained on the affinity column in step (b) and wherein the eluate prepared in step

(c) is enriched for RNA molecules with a length of from about 10 to about 200 nucleotides.

64. The method of claim 63, wherein the affinity column is washed between steps (a) and (b).

65. The method of claim 64, wherein the wash solution contains an alcohol.

66. The method of claim 65, wherein the alcohol is ethanol.

67. The method of claim 63, wherein the affinity columns comprises glass fibers.

68. The method of claim 63, wherein the alcohol is selected from the group consisting of methanol, ethanol, propanol, isopropanol, butanol, isobutyl alcohol, tertiary butyl alcohol, 1-hexanol, 2-hexanol, and 3-hexanol.

69. The method of claim 63, wherein the alcohol is ethanol.

70. The method of claim 63, wherein the alcohol is isopropanol.

71. The method of claim 63, wherein the alcohol concentration is between about 10% and about 50%.

72. The method of claim 63, wherein the RNA molecules which are retained on the column are eluted with a solution which contains an alcohol at a concentration between about 0% and about 10%.

73. The method of claim 63, wherein the RNA molecules which are retained on the column range in length from about 15 to about 100 nucleotides.

74. The method of claim 63, wherein the RNA molecules which are retained on the column range in length from about 18 to about 50 nucleotides.

75. The method of claim 63, wherein the RNA molecules which are retained on the column range in length from about 20 to about 30 nucleotides.

76. The method of claim 63, wherein the RNA molecules are microRNA molecules.

77. The method of claim 63, wherein the RNA molecules are shRNA molecules.

78. The method of claim 63, wherein the RNA molecules are produced by in vitro transcription.

79. The method of claim 63, wherein the RNA molecules are digested with an enzyme prior to step (a).

80. The method of claim 79, wherein the enzyme is a ribonuclease.

81. The method of claim 80, wherein said ribonuclease is a member of the RNase III family of ribonucleases.

82. The method of claim 80, wherein said ribonuclease is selected from the group consisting of a DICER, an RNase III, an RNase A, RNase T1 and nuclease S1.

83. A method for separating RNA molecules which differ in length, the method comprising:

(a) preparing a mixture comprising;

(i) a population of RNA molecules which vary in length; and

(ii) an alcohol;

(b) applying the mixture of (a) to a first affinity column;

(c) collecting the first affinity column flow through;

(d) adding additional alcohol to the first affinity column flow through collected in step (c) to produce a solution;

(e) applying the solution prepared in step (d) to a second affinity column; and

(f) eluting RNA molecules which are retained on the second affinity column to produce an eluate;

wherein the eluate prepared in step (f) is enriched for RNA molecules with a length of from about 10 to about 100 nucleotides.

84. The method of claim 83, wherein the first and second affinity columns comprise glass fibers.

85. The method of claim 83, wherein the alcohol in at least one of steps (a) or (d) is selected from the group consisting of methanol, ethanol, propanol, isopropanol, butanol, isobutyl alcohol, tertiary butyl alcohol, 1-hexanol, 2-hexanol, and 3-hexanol.

86. The method of claim 85, wherein the alcohol is ethanol.

87. The method of claim 85, wherein the alcohol is isopropanol.

88. The method of claim 83, wherein the alcohol concentration in step (a) is between about 10% and about 40%.

89. The method of claim 83, wherein the alcohol concentration of the solution prepared in step (d) is between about 40% and about 95%.

90. The method of claim 83, wherein the RNA molecules are eluted in step (f) with a solution which contains no alcohol.

91. The method of claim 83, wherein the RNA molecules are microRNA molecules.

92. The method of claim 83, wherein the RNA molecules are shRNA molecules.

93. A kit comprising a DICER enzyme and at least one component selected from the group consisting of:

(a) an affinity column;

(b) a solution which contains at least one alcohol;

(c) a transfection agent;

(d) a vector; and

(e) one more sets of instructions.

94. The kit of claim 93, further comprising primers for directing transcription of said vector.

95. The kit of claim 94, further comprising an RNA polymerase that catalyzes transcription of said vector.

96. The kit of claim 95, wherein said RNA polymerase is selected from the group consisting of T3 RNA polymerase, T7 RNA polymerase, and SP6 RNA polymerase.

97. The kit of claim 93, wherein said affinity column comprises glass fibers.