Methods and compositions for analysis of regulatory sequences

• US 20060166206A1
• Filed: 11/17/2003
• Published: 07/27/2006
• Est. Priority Date: 11/15/2002
• Status: Abandoned Application

• Current Assignee: Sangamo Biosciences, Inc.
• Original Assignee: Sangamo Biosciences, Inc.
• Inventors: Urnov, Fyodor, Rhodes, Eric
• Application Number:
  US10/533,847
• Publication Number:
  US 20060166206A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12N 15/1034 Isolating an individual clone by screening libraries
• CPC Class Codes: C12Q 1/6837 using probe arrays or probe chips C12Q1/6874 takes precedence

Abstract

Methods for constructing arrays of regulatory sequences, and the arrays so obtained, are provided. Regulatory sequences for use on the arrays are isolated based on their accessibility in cellular chromatin. A number of methods for using the arrays are disclosed, including regulatory DNA profiling, epigenome profiling, toxicological profiling and identification of in vivo binding sites of DNA binding proteins in complex genomes.

Claims

1. A method for making an array, the method comprising:

(a) isolating a plurality of cellular polynucleotide sequences, whereby the sequences are isolated based on their accessibility in cellular chromatin; and

(b) attaching each of the isolated sequences to an address on a solid support.

2. An array comprising a plurality of accessible polynucleotide sequences, wherein:

(a) the sequences are isolated based on their accessibility in cellular chromatin; and

(b) each accessible sequence is located at a distinct address on a solid support.

3. The array of claim 2, wherein the accessible sequences are isolated from a plurality of different cell types from an organism.

4. The array of claim 2, wherein the accessible sequences are isolated from a single cell or tissue type from an organism.

5. The array of claim 2, wherein the accessible sequences are isolated according to the following procedure:

(a) isolating a first plurality of cellular polynucleotide sequences, whereby the sequences are isolated based on their accessibility in cellular chromatin from a first cell;

(b) isolating a second plurality of cellular polynucleotide sequences, whereby the sequences are isolated based on their accessibility in cellular chromatin from a second cell;

(c) obtaining sequences that are unique to either the first or second plurality of cellular polynucleotide sequences; and

(d) attaching each of the isolated sequences obtained in step (c) to an address on a solid support.

6. A method of identifying a target sequence bound by a DNA-binding protein, the method comprising the steps of:

(a) contacting at least one DNA-binding protein with an array according to claim 2, under conditions such that the protein binds to accessible sequences comprising a target sequence bound by the protein;

(b) removing unbound proteins; and

(c) identifying the accessible sequences bound by the protein, thereby identifing target sequences for the protein.

7. A method of identifying a transcription factor, the method comprising the steps of:

(a) preparing a preparation of proteins from a cell;

(b) contacting the isolated proteins with an array according to claim 2, under conditions such that transcription factors in the protein preparation bind to accessible sequences comprising a target sequence bound by a transcription factor;

(c) removing unbound proteins; and

(d) identifying the proteins bound to the array.

8. A method for obtaining a regulatory profile of accessible sequences in a cell, the method comprising:

(a) isolating a plurality of polynucleotide sequences from the cell, whereby the sequences are isolated based on their accessibility in cellular chromatin;

(b) optionally amplifying the sequences obtained in step (a);

(c) optionally labeling the sequences of step (a) or (b);

(d) contacting the sequences of step (a), (b) or (c) with an array according to claim 3;

and

(e) identifying the accessible sequences bound on the array, thereby identifying sequences that are accessible in the cell.

9. A method for identifying functional binding sites for a DNA-binding protein in a cell, the method comprising:

(a) subjecting a cell to conditions under which DNA-binding proteins are crosslinked to their binding sites in cellular chromatin;

(b) shearing the crosslinked cellular chromatin of step (a);

(c) inmrunoprecipitating the sheared crosslinked chromatin of step (b) with an antibody which recognizes the DNA-binding protein;

(d) reversing the crosslinks in the immunoprecipitate of step (c);

(e) purifying the DNA from the irnmunoprecipitated material of step (d);

(f) optionally amplifying the DNA obtained in step (e);

(g) optionally labeling the DNA of step (e) or (f);

(h) contacting the DNA from step (e), (f) or (g) with an array according to claim 2;

and

(i) identifying the accessible sequences bound on the array, thereby identifying functional binding sites for the DNA-binding protein in the cell.

10. A method of identifying a sequence in cellular chromatin, wherein the chromatin is covalently modified, the method comprising:

(a) providing a sample of cellular chromatin;

(b) optionally subjecting the chromatin of step (a) to conditions under which DNA-binding proteins are crosslinked to their binding sites in cellular chromatin;

(c) shearing the cellular chromatin of step (a) or (b);

(d) immunoprecipitating the sheared chromatin of step (c) with an antibody which recognizes a covalent chromatin modification;

(e) purifying the DNA from the immunoprecipitated material of step (d);

(f) optionally amplifying the DNA obtained in step (e);

(g) optionally labeling the DNA of step (e) or (f);

(h) contacting the DNA from step (e), (f) or (g) with an array according to claim 2;

and

(i) identifying the accessible sequences bound on the array, thereby identifying sequences in cellular chromatin wherein the chromatin is covalently modified.

11. A method for characterizing the effects of a molecule on a cell, the method comprising:

(a) contacting the cell with the molecule;

(b) isolating a first plurality of polynucleotide sequences from the cell of step (a), whereby the sequences are isolated based on their accessibility in cellular chromatin;

(c) optionally amplifying the sequences obtained in step (b);

(d) optionally labeling the sequences of step (b) or (c);

(e) contacting the sequences of step (b), (c) or (d) with an array according to claim 2;

and

(f) identifying the accessible sequences bound on the array, thereby identifying sequences that are accessible in the cell.

12. The method of claim 11, further comprising the steps of:

(g) providing cells that have not been contacted with the molecule;

(h) isolating a second plurality of polynucleotide sequences from the cell of step (g), whereby the sequences are isolated based on their accessibility in cellular chromatin;

(i) optionally amplifying the sequences obtained in step (h);

(j) obtaining sequences that are unique to either the first or second plurality of polynucleotide sequences;

(k) optionally amplifying the sequences obtained in step (j);

(l) optionally labeling the sequences of step (j) or (k);

(m) contacting the sequences of step (j), (k) or (1) with an array according to claim 2;

and

(n) identifying the accessible sequences bound on the array, thereby identifying differences in accessible sequences between cells that have and have not been contacted with the molecule.

13. A method of identifying single nucleotide polymorphisms (SNPs) in regulatory sequences of an individual, the method comprising the steps of:

(a) preparing a library of regulatory DNA sequences from chromatin isolated from cells from the individual;

(b) optionally labeling the sequences of step (a);

(c) hybridizing the sequences of step (a) or (b) to an array according to claim 2 under stringent hybridization conditions, wherein the regulatory DNA sequences of the library hybridize to complementary accessible sequences on the array;

(d) removing regulatory DNA sequences of the library that are not bound to accessible sequences on the array; and

(e) identifying accessible sequences on the array that are not hybridized to regulatory DNA sequences of the library, wherein the unbound accessible sequences on the array suggest the presence of a SNP in regulatory sequences of the individual corresponding to the unbound accessible sequence.

14. A method for characterizing the effects of a stimulus on a cell, the method comprising:

(a) subjecting the cell to the stimulus;

(b) isolating a first plurality of polynucleotide sequences from the cell of step (a), whereby the sequences are isolated based on their accessibility in cellular chromatin;

(c) optionally amplifying the sequences obtained in step (b);

(d) optionally labeling the sequences of step (b) or (c);

(e) contacting the sequences of step (b), (c) or (d) with an array according to claim 2;

and

(f) identifying the accessible sequences bound on the array, thereby identifying sequences that are accessible in the cell.

15. The method of claim 14, further comprising the steps of:

(g) providing cells that have not been subjected to the stimulus;

(h) isolating a second plurality of polynucleotide sequences from the cell of step (g), whereby the sequences are isolated based on their accessibility in cellular chromatin;

(i) optionally amplifying the sequences obtained in step (h);

(j) obtaining sequences that are unique to either the first or second plurality of polynucleotide sequences;

(k) optionally amplifying the sequences obtained in step (j);

(l) optionally labeling the sequences of step (j) or (k);

(m) contacting the sequences of step (j), (k) or (l) with an array according to claim 2;

and

(n) identifying the accessible sequences bound on the array, thereby identifying differences in accessible sequences between cells that have and have not been subjected to the stimulus.