IP Library Granted Patent US 11,401,552
Granted Patent B2
US 11,401,552 · App. 15/750,715 · Granted Aug 2, 2022

Methods of identifying male fertility status and embryo quality

Inventors: Douglas T. Carrell (Salt Lake City, UT); Bradley Cairns (Salt Lake City, UT); Kenneth I. Aston (Salt Lake City, UT); Timothy Jenkins (Salt Lake City, UT); Andrew David Smith (Los Angeles, CA); Philip James Uren (Pasadena, CA); Alan Horsager (Pasadena, CA)
Assignees: University of Utah Research Foundation; The University of Southern California
C12Q1/6883A61B17/43C12Q1/68G16B20/00C12Q2600/112C12Q2600/118C12Q2600/154G01N2800/367
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Quick Facts
Patent No.
US 11,401,552
App. No.
15/750,715
Granted
Aug 2, 2022
Kind
B2
Abstract

Methods are provided of identifying a male fertility condition in a subject. Methods of performing a fertility treatment and an in vitro fertilization procedure are also provided. The methods may comprise determining the DNA methylation pattern of DNA extracted from a semen sample of a subject.

Claims (34)

1. A method comprising:

(a) extracting a DNA from a semen sample from a male subject;

(b) generating a methylation pattern of at least a portion of the extracted DNA, wherein the generating comprises:

converting unmethylated cytosines to uracils in at least a portion of the extracted DNA to form converted DNA,

(ii) hybridizing the converted DNA to a microarray,

(iii) scanning the microarray, and

(iv) with a first computer program, executed on a computer, generating Beta-values for a plurality of CpG sites, thereby generating the methylation pattern;

(c) with a second computer program, executed on a computer, detecting a difference between the methylation pattern of the extracted DNA and a control pattern of DNA methylation, wherein the difference comprises aberrant methylation associated with at least five genes of the following genes: AHDC1, ALOX5AP, BTBD17, CXXC11, EEF1A2, FBLN2, FGF18, GRM6, HIST1H4J, HIST1H4K, KIAA0319L, LRRC45, MIR4734, MLLT6, MTMR6, MXRA7, NCDN, NDUFS6, NDUFS8, OGFOD2, SERPINF2, STRA13, SYT8, TCIRG1, and TNNI2; and

(d) performing a fertility treatment with the semen of the male subject, wherein the fertility treatment comprises in vitro fertilization or artificial insemination.

2. The method of claim 1 , wherein the control pattern of DNA methylation is obtained from a plurality of semen samples from fertile male subjects.

3. The method of claim 1 , wherein the control pattern of DNA methylation is obtained from a plurality of semen samples from male subjects with at least partially diminished infertility.

4. The method of claim 1 , wherein the methylation pattern of the extracted DNA is a genome-wide methylation pattern, wherein the genome-wide methylation pattern comprises the methylation at a plurality of loci across the genome.

5. The method of claim 1 , wherein the methylation pattern of the extracted DNA comprises a methylation status of at least 50,000 cytosine-guanine dinucleotides (CpGs) from the extracted DNA.

6. The method of claim 1 , wherein the methylation pattern of the extracted DNA comprises a methylation status of at least 50,000 cytosines from the extracted DNA.

7. The method of claim 1 , wherein the aberrant methylation independently comprises, for each of the genes associated with the aberrant methylation, increased methylation or decreased methylation, compared to the control pattern of DNA methylation at the same gene.

8. The method of claim 1 , wherein the first computer program and the second computer program are the same.

9. The method of claim 1 , wherein the first computer program and the second computer program are different computer programs.

10. The method of claim 1 , further comprising performing an assisted reproductive technology using the sperm of the male subject.

11. The method of claim 1 , wherein the converting unmethylated cytosines to uracils comprises a bisulfite treatment.

12. A method comprising:

(a) extracting a DNA from a semen sample from a male subject;

(b) generating a methylation pattern of at least a portion of the extracted DNA, wherein the generating comprises:

(i) converting unmethylated cytosines to uracils in at least a portion of the extracted DNA to form converted DNA,

(ii) sequencing the converted DNA, and

(iii) with a first computer program, generating a methylation pattern;

(c) with a second computer program, executed on a computer, detecting a difference between the methylation pattern of the extracted DNA and a control pattern of DNA methylation, wherein the difference comprises aberrant methylation associated with at least five genes of the following genes: AHDC1, ALOX5AP, BTBD17, CXXC11, EEF1A2, FBLN2, FGF18, GRM6, HIST1H4J, HIST1H4K, KIAA0319L, LRRC45, MIR4734, MLLT6, MTMR6, MXRA7, NCDN, NDUFS6, NDUFS8, OGFOD2, SERPINF2, STRA13, SYT8, TCIRG1, and TNNI2; and

(d) performing a fertility treatment with the semen of the male subject, wherein the fertility treatment comprises in vitro fertilization or artificial insemination.

13. The method of claim 12 , wherein the control pattern of DNA methylation is obtained from a plurality of semen samples from fertile male subjects.

14. The method of claim 12 , wherein the control pattern of DNA methylation is obtained from a plurality of semen samples from male subjects with at least partially diminished infertility.

15. The method of claim 12 , wherein the methylation pattern of the extracted DNA is a genome-wide methylation pattern, wherein the genome-wide methylation pattern comprises the methylation at a plurality of loci across the genome.

16. The method of claim 12 , wherein the methylation pattern of the extracted DNA comprises a methylation status of at least 50,000 cytosines from the extracted DNA.

17. The method of claim 12 , wherein the aberrant methylation independently comprises, for each of the genes associated with the aberrant methylation, increased methylation or decreased methylation, compared to the control pattern of DNA methylation at the same gene.

18. The method of claim 12 , wherein the first computer program and the second computer program are the same.

19. The method of claim 12 , wherein the first computer program and the second computer program are different computer programs.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2019
From: CARRELL, DOUGLAS T.; CAIRNS, BRADLEY; ASTON, KENNETH I.; JENKINS, TIMOTHY
To: UNIVERSITY OF UTAH
Reel/Frame 049001/0698 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2019
From: UNIVERSITY OF UTAH
To: UNIVERSITY OF UTAH RESEARCH FOUNDATION
Reel/Frame 049001/0749 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2019
From: SMITH, ANDREW DAVID
To: THE UNIVERSITY OF SOUTHERN CALIFORNIA
Reel/Frame 049001/0844 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2019
From: UREN, PHILIP JAMES; HORSAGER, ALAN
To: EPISONA, INC.
Reel/Frame 049001/0937 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2019
From: EPISONA, INC.
To: UNIVERSITY OF UTAH RESEARCH FOUNDATION
Reel/Frame 049001/0955 →
Continuity (2)
Provisional Application 62201907 · Aug 6, 2015
Related Publication 20190112659A1 · Apr 18, 2019