Massively multiplexed RNA sequencing

Patent metadata

Field	Value
Publication number	US-10612088-B2
Application number	US-201414774648-A
Country	US
Kind code	B2
Filing date	Mar 14, 2014
Priority date	Mar 14, 2013
Publication date	Apr 7, 2020
Grant date	Apr 7, 2020

Abstract

A method for parallel sequencing target RNA from samples from multiple sources while maintaining source identification is provided. The method includes providing samples of RNA comprising target RNA from two or more sources; labeling, at the 3′ end, the RNA from the two or more sources with a first nucleic acid adaptor that comprises a nucleic acid sequence that differentiates between the RNA from the two or more sources; reverse transcribing the two or more sources to create a single stranded DNA comprising the nucleic acid sequence that differentiates between the RNA from the two or more sources; amplifying the single stranded DNA to create DNA amplification products that comprise the nucleic acid sequence that differentiates between the RNA from the two or more sources; sequencing the DNA amplification products thereby parallel sequencing target RNA from samples from multiple sources while maintaining source identification.

First claim

We claim:

1. A method for parallel sequencing target RNA from samples from multiple sources while maintaining source identification, comprising:
providing samples of RNA comprising target RNA from two or more sources;
labeling, at the 3′ end, the target RNA with a first nucleic acid adaptor that is at least two nucleotides in length and comprises a nucleic acid sequence that is indexed to the origin or source of the sample and differentiates between the RNA from the two or more sources;
pooling the 3′ labeled RNA;
reverse transcribing the 3′ labeled RNA from the two or more sources to create a single stranded DNA comprising the nucleic acid sequence that differentiates between the RNA from the two or more sources;
amplifying the single stranded DNA to create DNA amplification products that comprise the nucleic acid sequence that differentiates between the RNA from the two or more sources;
sequencing the DNA amplification products; thereby parallel sequencing target RNA from samples from multiple sources while maintaining source identification.

2. The method of claim 1 , further comprising labeling, at the 3′ end, the single stranded DNA with a second nucleic acid adaptor that comprises a site for binding of a PCR primer wherein the second nucleic acid adaptor optionally comprises a sequencing adaptor and/or a second nucleic acid sequence that can differentiate between single stranded DNA from two or more sources.

3. The method of claim 1 , wherein the first nucleic acid adaptor comprises a sequencing adaptor.

4. The method of claim 3 , further comprising pooling the single stranded DNA with single stranded DNA from one or more additional sources, wherein the single stranded DNA from the one or more additional sources is similarly labeled.

5. The method of claim 1 , further comprising depleting the samples of non-target RNA.

6. The method of claim 5 , wherein depleting the samples of non-target RNA comprises using one or more probes that specifically hybridize to the non-target RNA, wherein the one or more probes comprise a label that facilitates removal of the probe from the sample.

7. The method of claim 1 , wherein the first nucleic acid adaptor is 3′ end blocked and/or wherein the first nucleic acid adaptor comprises RNA, DNA or a RNA-DNA hybrid.

8. The method of claim 2 , wherein the second nucleic acid adaptor is 3′ end blocked and/or wherein the second nucleic acid adaptor comprises RNA, DNA or a RNA-DNA hybrid.

9. The method of claim 2 , wherein the nucleic acid sequence that differentiates between the single stranded DNA from the two or more sources is at least two nucleotides in length.

10. The method of claim 1 , further comprising removing and/or degrading the reverse transcription primers and/or removing and/or degrading the RNA from the sample.

11. The method of claim 1 , wherein the samples of different origins comprise samples of the same cell type and/or tissue type exposed to different environmental conditions.

12. The method of claim 11 , wherein the different environmental conditions are contacts with different test agents.

13. The method of claim 1 , where the target RNA is mRNA, and differences in expression of the mRNA are measured across samples from different sources.

14. The method of claim 1 , further comprising quantifying the sequenced target RNAs of samples from multiple sources.

15. The method of claim 1 , comprising sorting the sequenced target RNAs to their respective sources.

16. The method of claim 1 , further comprising labeling, at the 5′ end, the RNA from the two or more sources with a first nucleic acid adaptor that comprises a nucleic acid sequence that differentiates between the RNA from the two or more sources.

17. The method of claim 16 , further comprising labeling, at the 5′ end, the single stranded DNA with a second nucleic acid adaptor that comprises a site for binding of a PCR primer and/or a sequencing adaptor.

Assignees

• Broad Inst Inc
• Massachusetts Inst Technology

Inventors

• Shishkin Alexander A
• Guttman Mitchell
• Surka Christine F
• Lander Eric S

Classifications

• C12Q2563/179

  the label being a nucleic acid · CPC title

• C12Q1/6874 Primary

  involving nucleic acid arrays, e.g. sequencing by hybridisation · CPC title

• C12Q1/6806

  Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay (C12Q1/6804 takes precedence) · CPC title

• C12Q2521/107

  RNA dependent DNA polymerase,(i.e. reverse transcriptase) · CPC title

• C12Q2535/122

  Massive parallel sequencing · CPC title