Hadziselimovic Faruk, Verkauskas Gilvydas, Stadler Michael B
Cryptorchidism Research Institute, Children's Day Care Center, 4410, Liestal, Switzerland.
Children's Surgery Centre, Faculty of Medicine, Vilnius University, 01513, Vilnius, Lithuania.
Basic Clin Androl. 2023 Sep 21;33(1):24. doi: 10.1186/s12610-023-00199-7.
Cryptorchid boys with defective mini-puberty and impaired differentiation of Ad spermatogonia (high infertility risk) have altered expression of several genes encoding histone methyltransferases compared to patients with intact differentiation of gonocytes into Ad spermatogonia (low infertility risk).
High infertility risk cryptorchid boys display hypogonadotropic hypogonadism, which, together with the diminished expression of histone deacetylases and increased expression of HDAC8 decrotonylase, indicates altered histone marks and, thus, a perturbed histone code. Curative GnRHa treatment induces normalization of histone methyltransferase, chromatin remodeling, and histone deacetylase gene expression. As a result, histone changes induce differentiation of Ad spermatogonia from their precursors and, thus, fertility. In this short report, we describe key functions of histone lysine methyltransferases, chromatin remodeling proteins, and long-noncoding RNAs, and discuss their potential roles in processes leading to infertility.
Our findings suggest that epigenetic mechanisms are critical to better understanding the root causes underlying male infertility related to cryptorchidism and its possible transgenerational transmission.
与生殖母细胞完整分化为A1型精原细胞(低不孕风险)的患者相比,青春期小阴茎功能缺陷且A1型精原细胞分化受损(高不孕风险)的隐睾男孩,几种编码组蛋白甲基转移酶的基因表达发生了改变。
高不孕风险的隐睾男孩表现为低促性腺激素性性腺功能减退,这与组蛋白去乙酰化酶表达减少和HDAC8去巴豆酰化酶表达增加一起,表明组蛋白标记发生改变,从而导致组蛋白密码紊乱。治愈性促性腺激素释放激素类似物(GnRHa)治疗可诱导组蛋白甲基转移酶、染色质重塑和组蛋白去乙酰化酶基因表达正常化。结果,组蛋白变化诱导A1型精原细胞从前体细胞分化,从而恢复生育能力。在本简短报告中,我们描述了组蛋白赖氨酸甲基转移酶、染色质重塑蛋白和长链非编码RNA的关键功能,并讨论了它们在导致不孕的过程中的潜在作用。
我们的研究结果表明,表观遗传机制对于更好地理解与隐睾症相关的男性不育的根本原因及其可能的跨代遗传至关重要。