Steilmann C, Paradowska A, Bartkuhn M, Vieweg M, Schuppe H-C, Bergmann M, Kliesch S, Weidner W, Steger K
Department of Urology, Pediatric Urology and Andrology, Justus-Liebig University of Giessen, Rudolf Buchheim Str. 7, 35385 Giessen, Germany.
Reprod Fertil Dev. 2011;23(8):997-1011. doi: 10.1071/RD10197.
During spermatogenesis, approximately 85% of histones are replaced by protamines. The remaining histones have been proposed to carry essential marks for the establishment of epigenetic information in the offspring. The aim of the present study was to analyse the expression pattern of histone H3 acetylated at lysine 9 (H3K9ac) during normal and impaired spermatogenesis and the binding pattern of H3K9ac to selected genes within ejaculates. Testicular biopsies, as well as semen samples, were used for immunohistochemistry. Chromatin immunoprecipitation was performed with ejaculated sperm chromatin. HeLa cells and prostate tissue served as controls. Binding of selected genes was evaluated by semiquantitative and real-time polymerase chain reaction. Immunohistochemistry of H3K9ac demonstrated positive signals in spermatogonia, spermatocytes, elongating spermatids and ejaculated spermatozoa of fertile and infertile men. H3K9ac was associated with gene promoters (CRAT, G6PD, MCF2L), exons (SOX2, GAPDH, STK11IP, FLNA, PLXNA3, SH3GLB2, CTSD) and intergenic regions (TH) in fertile men and revealed shifts of the distribution pattern in ejaculated spermatozoa of infertile men. In conclusion, H3K9ac is present in male germ cells and may play a role during the development of human spermatozoa. In addition, H3K9ac is associated with specific regions of the sperm genome defining an epigenetic code that may influence gene expression directly after fertilisation.
在精子发生过程中,约85%的组蛋白被鱼精蛋白取代。其余的组蛋白被认为携带了在后代中建立表观遗传信息的关键标记。本研究的目的是分析在正常和受损精子发生过程中赖氨酸9乙酰化的组蛋白H3(H3K9ac)的表达模式以及H3K9ac与射精样本中选定基因的结合模式。睾丸活检组织以及精液样本用于免疫组织化学分析。对射出的精子染色质进行染色质免疫沉淀。HeLa细胞和前列腺组织作为对照。通过半定量和实时聚合酶链反应评估选定基因的结合情况。H3K9ac的免疫组织化学分析显示,在可育和不育男性的精原细胞、精母细胞、伸长的精子细胞和射出的精子中均有阳性信号。在可育男性中,H3K9ac与基因启动子(CRAT、G6PD、MCF2L)、外显子(SOX2、GAPDH、STK11IP、FLNA、PLXNA3、SH3GLB2、CTSD)和基因间区域(TH)相关,并且在不育男性射出的精子中分布模式发生了变化。总之,H3K9ac存在于雄性生殖细胞中,可能在人类精子发育过程中发挥作用。此外,H3K9ac与精子基因组的特定区域相关,定义了一种表观遗传密码,可能在受精后直接影响基因表达。