作为一种分子特征的表观遗传干扰在非异常非阻断性亚子精子症中的分子特征
Amir Masoud Firouzabadi1,2, Samaneh Harimi2, Parisa Heydari2,3
1Department of Biology, Ashk.C., Islamic Azad University, Ashkezar, Yazd, Iran.
American journal of men's health
|November 17, 2025
概括
表观遗传调节剂DNA甲基转移酶3B (DNMT3B) 和含指CCHC-类型13 (ZCCHC13) 显示在异形非阻断性精 (iNOA) 中表达的改变. 这些表观遗传生物标志物可能有助于诊断iNOA,并指导未来的治疗方法.
科学领域:
- 生殖生物学 生殖生物学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 分子遗传学 分子遗传学
背景情况:
- 当没有发现精子缺失的原因时,诊断为异形非阻塞性精子缺失 (iNOA).
- 表观遗传变化与精子生成功能障碍有关.
研究的目的:
- 为了比较DNA甲基转移酶 (DNMT) 1 (DNMT1),DNMT3A,DNMT3B和含有13 (ZCCHC13) 的指CCHC类型的DNA甲基转移酶 (DNMT) 1 (DNMT1),iNOA中的基因表达与阻断性亚子精子症 (OA) 的基因表达.
- 评估iNOA中这些表观遗传调节者的诊断潜力.
主要方法:
- 使用定量实时PCR分析DNMT1,DNMT3A,DNMT3B和ZCCHC13表达在60名亚精子男性 (30iNOA,30OA) 的丸组织中.
- iNOA患者被分为成功的 (iNOA+) 和不成功的 (iNOA-) 精子采集组,基于微切割丸精子提取 (micro-TESE).
- 接收器操作特征 (ROC) 分析评估了诊断准确性.
主要成果:
- 与OA相比,iNOA中的DNMT1和ZCCHC13表达显著较低 (p = .01).与OA相比,iNOA中的DNMT1和ZCCHC13表达显著较低 (p = .01).
- 在iNOA中,DNMT3B的表达显著更高,特别是在iNOA-亚组中 (p < .0001).
- DNMT3B显示了最高的诊断准确性 (AUC = 0.84),其次是ZCCHC13 (AUC = 0.69) 和DNMT1 (AUC = 0.68).
结论:
- 表观遗传失调,特别是涉及DNMT3B和ZCCHC13,有助于iNOA中的精子发生障碍.
- 这些表观遗传生物标志物有可能从分子上区分iNOA和OA,并指导治疗策略.
相关概念视频
Nondisjunction
4.8K
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers. Nondisjunction is common during anaphase I or anaphase II of meiosis. Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold...
4.8K
Infertility in Males
519
Male infertility affects millions of couples worldwide, arising from various factors that impact different stages of the reproductive process. An endocrine imbalance resulting from conditions like hypogonadism, Klinefelter syndrome, or pituitary disorders can disrupt hormone levels and reduce sperm production. Testicular defects, such as tumors, cryptorchidism, atrophic testes, abnormal sperm morphology, and low sperm count or motility, may arise due to genetic factors, structural...
519
Genomic Imprinting and Inheritance
36.8K
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
36.8K
Epigenetic Regulation
3.7K
Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
X-chromosome...
3.7K
Oogenesis
68.9K
In human women, oogenesis produces one mature egg cell or ovum for every precursor cell that enters meiosis. This process differs in two unique ways from the equivalent procedure of spermatogenesis in males. First, meiotic divisions during oogenesis are asymmetric, meaning that a large oocyte (containing most of the cytoplasm) and minor polar body are produced as a result of meiosis I, and again following meiosis II. Since only oocytes will go on to form embryos if fertilized, this unequal...
68.9K


