患有Bag5缺陷的男性生殖细胞显示精子生成和基本核蛋白的交换减少
Yuming Cao1, Shengnan Wang1, Zihan Qin2,3
1Department of Obstetrics and Gynecology, Perinatal Medical Center, The Fifth Affiliated Hospital of Sun Yat-Sen University, No. 52 Meihua East Road, Zhuhai, Guangdong, People's Republic of China.
Cellular and molecular life sciences : CMLS
|February 24, 2025
概括
与Bcl-2相关的乙基-5 (BAG5) 对男性生育能力至关重要,它调节精子发育和核蛋白沉积. 它的缺乏通过影响HSPA2表达和生殖细胞亡导致不孕.
科学领域:
- 生殖生物学 生殖生物学
- 分子遗传学 分子遗传学
- 细胞生物学 细胞生物学
背景情况:
- 与Bcl-2相关的乙基-5 (BAG5) 是一种参与调节伴侣活性的协伴蛋白.
- BAG5在丸中表达高,对精子生成至关重要.
- 改变BAG5表达与男性不孕症有关,但潜在的机制尚不清楚.
研究的目的:
- 研究BAG5在男性生育中的作用及其分子机制.
- 探索BAG5,HSPA2和精子生成之间的关系.
- 评估BAG5作为男性不孕不育的潜在生物标志物.
主要方法:
- 精子和丸样本的RNA测序分析来自健康和不育的个体.
- 在小鼠中对Bag5的向基因失活.
- 免疫沉质谱 (IP-MS) 用于识别蛋白质相互作用.
- 评估生殖细胞的亡,核蛋白沉积和染色质凝结.
主要成果:
- 在小鼠中,Bag5的失活导致了生殖细胞的亡,不孕症,核蛋白负载的改变和精子头部的变形.
- BAG5与HSPA2相互作用,HSPA2是精子生成和过渡蛋白 (TNPs) 的关键调节者.
- Bag5 缺陷降低了HSPA2 水平,破坏了染色质凝结,并与非阻塞性亚精和橄酸精相关.
结论:
- BAG5在男性生殖细胞发育和染色体组织中起着关键的HSPA2介导作用.
- BAG5 缺乏导致通过胚胎细胞亡和核蛋白沉积受损的男性不孕症.
- BAG5可以作为男性不孕症的预后生物标志物.
相关概念视频
Spermatogenesis
102.0K
Spermatogenesis is the process by which haploid sperm cells are produced in the male testes. It starts with stem cells located close to the outer rim of seminiferous tubules. These spermatogonial stem cells divide asymmetrically to give rise to additional stem cells (meaning that these structures “self-renew”), as well as sperm progenitors, called spermatocytes. Importantly, this method of asymmetric mitotic division maintains a population of spermatogonial stem cells in the male...
102.0K
Sex-linked Disorders
99.9K
Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
99.9K
Infertility in Males
230
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...
230
The Y Chromosome Determines Maleness
6.5K
The Y chromosome is a sex chromosome found in several vertebrates and mammals, including humans. In addition to 22 pairs of autosomes, the human males have one X chromosome and one Y chromosome. In these organisms, the presence or absence of the Y chromosome determines the development of male traits.
Evolution
Around 300 million years ago, the two sex chromosomes diverged from two identical autosomal chromosomes. Over time, the Y chromosome has lost most of its genes, shrinking in size....
Evolution
Around 300 million years ago, the two sex chromosomes diverged from two identical autosomal chromosomes. Over time, the Y chromosome has lost most of its genes, shrinking in size....
6.5K
X and Y Chromosomes
21.4K
Among mammals, the gender of an organism is determined by the sex chromosomes. Humans have two sex chromosomes, X and Y. Every human diploid cell has 22 pairs of autosomes and one pair of sex chromosomes. A human female has two X chromosomes, while a male has one X chromosome and one Y chromosome.
The germline cells such as egg and sperm cells carry only half the number of chromosomes, i.e., 22 autosomes and one sex chromosome. All eggs have an X chromosome, while sperm cells can carry an X or...
The germline cells such as egg and sperm cells carry only half the number of chromosomes, i.e., 22 autosomes and one sex chromosome. All eggs have an X chromosome, while sperm cells can carry an X or...
21.4K
Nondisjunction
3.7K
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...
3.7K


