Method of cytogenetic analysis

• US 5,427,910 A
• Filed: 12/09/1992
• Issued: 06/27/1995
• Est. Priority Date: 12/09/1992
• Status: Expired due to Fees

• Current Assignee: Compucyte Corporation (Thorlabs Incorporated)
• Original Assignee: Compucyte Corporation (Thorlabs Incorporated)
• Inventors: Kamentsky, Lee D., Kamentsky, Louis A.
• Primary Examiner(s): Parr, Margaret
• Assistant Examiner(s): Marschel, Ardin H.
• Application Number:
  US07/987,679
• Time in Patent Office: 930 Days
• Field of Search: 435/6, 435/91, 435/810, 435/91.1, 435/912, 436/501, 436/63, 536/22.1, 536/23.1, 536/24.1, 536/24.2, 536/24.31-24.33, 935/78, 935/77
• US Class Current: 435/6.12
• CPC Class Codes: C12Q 1/6841 In situ hybridisation
• CPC Class Codes: Y10S 435/81 Packaged device or kit

Abstract

A method of characterizing the chromosomes in a sample of cells by fixing the cell sample on a substrate, contacting the cell sample with a nucleic acid probe having a detectable label under conditions that allow the probe to hybridize preferentially to a chromosome in the cells to form a hybridized complex, optically detecting each labeled complex in the sample, defining a predetermined number of neighboring labeled complexes as a group, generating a distance parameter based on the distance between the position of a group and the position of the next neighboring labeled complex, and comparing the distance parameter for each group to a standard distance value to characterize the chromosomes in the cells of the sample.

Claims

1. A method of determining the number of a specific type of chromosome per cell in a sample of cells comprising

(a) fixing the cell sample on a substrate,

(b) contacting the cell sample with a nucleic acid probe comprising a detectable label under conditions that allow said probe to hybridize preferentially to a target nucleotide sequence within said specific type of chromosome in said cells to form a hybridized complex, wherein each complex forms a labeled region,

(c) detecting each labeled region in the sample,

(d) assigning a position corresponding to each labeled region on the substrate,

(e) defining a predetermined number of nearest adjacent labeled regions as a region group and assigning a position on the substrate to each region group derived from said labeled region positions,

(f) generating a distance parameter for each region group based on the distance between the position of a region group and the position of the next nearest adjacent labeled region and recording the distance parameter for each region group in the sample, and

(g) comparing a population distribution of the distance parameters to a value based on the cellular nuclear diameter, and determining whether the closest regions are within the same cell, to determine the number of a specific type of chromosome per cell in the cells of the sample.

3. The method of claim 1 or 2, wherein said target nucleotide sequence is unique to a specific chromosome, said predetermined number of labeled regions in a region group is two, and said comparison step provides a determination of the number specific chromosomes in the cells of the sample, and wherein a distance parameter greater than said cellular nuclear diameter value indicates two chromosomes per cell, and a distance parameter less than said cellular nuclear diameter value indicates more than two chromosomes per cell, and indicates a genetic abnormality.

4. The method of claim 3, wherein said target sequence is unique to chromosome 21, and wherein cells having more than two chromosomes per cell indicate Down'"'"'s Syndrome.

5. The method of claim 1 or 2, wherein said target nucleotide sequence is unique to a specific type of chromosome, said predetermined number of labeled regions in a region group is one, and said comparison step provides a determination of the number of specific chromosomes in the cells of the sample, and wherein a distance parameter greater than said cellular nuclear diameter value indicates one chromosome per cell, and a distance parameter less than said cellular nuclear diameter value indicates more than one chromosome per cell.

6. The method of claim 5, wherein said target sequence is unique to chromosome X, and wherein cells having only one X chromosome per cell are from a male.

7. The method of claim 1 or 2, wherein more than one type of probe is used, each type of probe hybridizing preferentially to a unique target nucleotide sequence in said cells, and each type of probe having a unique detectable label, and wherein each of method steps (b) to (e) and (g) are carried out for each type of probe, and in method step (f) said labeled region corresponds to a first type of probe and said next neighboring labeled region of claim 1 and said Nth closest labeled region of claim 2 corresponds to a second type of probe.

8. The method of claim 1 or 2, wherein said cell sample is obtained from a mammal.

9. The method of claim 1 or 2, wherein said cell sample is obtained from a fetus.

10. The method of claim 1 or 2, wherein said label is fluorescent.

11. The method of claim 10, wherein said fluorescent label is fluorescein, rhodamine, or a cyanine dye.

12. The method of claim 1 or 2, further comprising the step of defining a threshold level below which no label is detected, and said label detecting step comprises measuring a level for each label in the sample, if any, and comparing the label level with said threshold level, a label being detected only when its level is above said threshold level.

2. A method of determining the number of a specific type of chromosome per cell in a sample of cells comprising

(a) fixing the cell sample on a substrate,

(b) contacting the cell sample with a nucleic acid probe comprising a detectable label under conditions that allow said probe to hybridize preferentially to a target nucleotide sequence within said specific type of chromosome in said cells to form a hybridized complex, wherein each complex forms a labeled region,

(c) detecting each labeled region in the sample,

(d) assigning a position corresponding to each labeled region on the substrate,

(e) defining a predetermined number N of labeled regions as a region group,

(f) generating a distance parameter for a selected labeled region based on the distance between the position of said selected labeled region and the position of the Nth closest labeled region, wherein the Nth closest labeled region is the Nth labelled region numbered sequentially by increasing distance from said selected labeled region, and recording the distance parameter for each labeled region in the sample, and

(g) comparing a population distribution of the distance parameters to a value based on the cellular nuclear diameter, and determining whether the closest labeled regions are within the same cell, to determine the number of a specific type of chromosome per cell in the cells of the sample.

13. A method of determining the number of a specific type of chromosome per cell in a sample of cells comprising

(a) fixing the cell sample on a substrate,

(b) contacting the cell sample with a nucleic acid probe comprising a detectable label under conditions that allow said probe to hybridize preferentially to a target nucleotide sequence within said specific type of chromosome in said cells to form a labeled hybridized complex,

(c) scanning the cell sample with a laser beam to generate an optical signal,

(d) detecting the optical signal and digitizing the detected signal to produce a set of digital data points,

(e) storing said set of digital data points,

(f) locating a region within the stored set of digital data points, said region comprising contiguous data points with digital values above a predetermined threshold value representing a labeled complex,

(g) assigning a position corresponding to each region on the substrate,

(h) defining a predetermined number of nearest adjacent regions as a region group and assigning a position on the substrate to each region group derived from said region positions,

(i) generating a distance parameter for each region group based on the distance between the position of a region group and the position of the next nearest adjacent region,

(j) recording the distance parameter for each detected region group, and

(k) comparing a population distribution of the distance parameters to a value based on the cellular nuclear diameter, and determining whether the closest regions are within the same cell, to determine the number of a specific type of chromosome per cell in the cells of the sample.

15. The method of claim 13 or 14, wherein said target nucleotide sequence is unique to a specific type of chromosome, said predetermined number of regions in a region group is two, and said comparison step provides a determination of the number of specific chromosomes in the cells of the sample, and wherein a distance parameter greater than said cellular nuclear diameter value indicates two chromosomes per cell, and a distance parameter less than said cellular nuclear diameter value indicates more than two of said specific chromosomes per cell, and indicates a genetic abnormality.

16. The method of claim 13 or 14, wherein said target nucleotide sequence is unique to a specific type of chromosome, said standard distance value is based on the cellular nuclear diameter, said predetermined number of regions in a region group is one, and said comparison step provides a determination of the number of specific chromosomes in the cells of the sample, and wherein a distance parameter greater than said cellular nuclear diameter value indicates one chromosome per cell, and a distance parameter less than said cellular nuclear diameter value indicates more than one chromosome per cell.

17. The method of claim 13 or 14, further comprising steps of

(a) summing the digital values in each region for each probe, and

(b) recording the summed digital values for each probe, wherein said values are proportional to the DNA copy number.

18. The method of claim 13 or 14, further comprising the step of moving the microscope stage to the assigned position of a region having a specific distance parameter so that the operator may observe cells visually.

19. The method of claim 13 or 14, wherein said optical signal is fluorescence.

20. The method of claim 13, wherein the position assigned to a region group corresponds to an average of the positions of peak intensity value of each region in said region group.

14. A method of determining the number of a specific type of chromosome per cell in a sample of cells comprising

(a) fixing the cell sample on a substrate,

(b) contacting the cell sample with a nucleic acid probe comprising a detectable label under conditions that allow said probe to hybridize preferentially to a target nucleotide sequence within said specific type of chromosome in said cells to form a labeled hybridized complex,

(c) scanning the cell sample with a laser beam to generate an optical signal,

(d) detecting the optical signal and digitizing the detected signal to produce a set of digital data points,

(e) storing said set of digital data points,

(f) locating a region within the stored set of digital data points, said region comprising contiguous data points with digital values above a predetermined threshold value representing a labeled complex,

(g) assigning a position corresponding to each region on the substrate,

(h) defining a predetermined number N of regions as a region group,

(i) generating a distance parameter for a selected region based on the distance between the position of said selected region and the position of the Nth closest region, wherein the Nth closest region is the Nth region numbered sequentially by increasing distance from said selected region,

(j) recording the distance parameter for each detected region, and

(k) comparing a population distribution of the distance parameters to a value based on the cellular nuclear diameter, and determining whether the closest detected regions are within the same cell, to determine the number of a specific type of chromosome per cell in the cells of the sample.

21. A method of determining whether two or more different specific nucleic acid probes in a cell in a sample of cells are on the same chromosome, comprising

(a) fixing the cell sample on a substrate,

(b) contacting the cell sample with a first nucleic acid probe comprising a detectable first label under conditions that allow said probe to hybridize preferentially to a first target nucleotide sequence within a chromosome in said cells to form a first labeled hybridized complex,

(c) contacting the cell sample with a second nucleic acid probe comprising a detectable second label under conditions that allow said probe to hybridize preferentially to a second target nucleotide sequence within a chromosome in said cells to form a second labeled hybridized complex,

(d) scanning the cell sample with a first laser beam having a first wavelength to excite said first label and generate a first optical signal,

(e) scanning the cell sample with a second laser beam having a second wavelength to excite said second label and generate a second optical signal,

(f) detecting and digitizing said first and second optical signals to produce two sets of digital data points,

(g) storing said sets of digital data points,

(h) for each data set, locating a region within the stored set of digital data points, said region comprising contiguous data points with digital values above a predetermined threshold value representing a labeled complex,

(i) for each data set, assigning a digital position corresponding to each region on the substrate,

(j) generating a digital distance parameter for a region based on the distance between the position of said region in said first data set to the nearest region in the second data set,

(k) recording the distance parameter for each detected region in the first data set, and

(1) comparing a population distribution of the distance parameters of the first data set to a value equal to an average inter-chromosomal distance in said cells to determine whether said first and second probes are on the same chromosome.

22. The method of claim 21, wherein said first wavelength and second wavelength laser beams scan the cell sample at a different time.