Department of Oncological Sciences, Howard Hughes Medical Institute, Salt Lake City, UT, USA.
Hum Reprod. 2011 Sep;26(9):2558-69. doi: 10.1093/humrep/der192. Epub 2011 Jun 17.
The sperm chromatin of fertile men retains a small number of nucleosomes that are enriched at developmental gene promoters and imprinted gene loci. This unique chromatin packaging at certain gene promoters provides these genomic loci the ability to convey instructive epigenetic information to the zygote, potentially expanding the role and significance of the sperm epigenome in embryogenesis. We hypothesize that changes in chromatin packaging may be associated with poor reproductive outcome.
Seven patients with reproductive dysfunction were recruited: three had unexplained poor embryogenesis during IVF and four were diagnosed with male infertility and previously shown to have altered protamination. Genome-wide analysis of the location of histones and histone modifications was analyzed by isolation and purification of DNA bound to histones and protamines. The histone-bound fraction of DNA was analyzed using high-throughput sequencing, both initially and following chromatin immunoprecipitation. The protamine-bound fraction was hybridized to agilent arrays. DNA methylation was examined using bisulfite sequencing.
Unlike fertile men, five of seven infertile men had non-programmatic (randomly distributed) histone retention genome-wide. Interestingly, in contrast to the total histone pool, the localization of H3 Lysine 4 methylation (H3K4me) or H3 Lysine 27 methylation (H3K27me) was highly similar in the gametes of infertile men compared with fertile men. However, there was a reduction in the amount of H3K4me or H3K27me retained at developmental transcription factors and certain imprinted genes. Finally, the methylation status of candidate developmental promoters and imprinted loci were altered in a subset of the infertile men.
This initial genome-wide analysis of epigenetic markings in the sperm of infertile men demonstrates differences in composition and epigenetic markings compared with fertile men, especially at certain imprinted and developmental loci. Although no single locus displays a complete change in chromatin packaging or DNA modification, the data suggest that moderate changes throughout the genome exist and may have a cumulative detrimental effect on fecundity.
生育能力正常男性的精子染色质保留了少量核小体,这些核小体在发育基因启动子和印迹基因座处富集。这种在特定基因启动子处的独特染色质包装赋予了这些基因组座向受精卵传递指导表观遗传信息的能力,这可能扩展了精子表观基因组在胚胎发生中的作用和意义。我们假设染色质包装的变化可能与生殖不良的结果有关。
招募了 7 名生殖功能障碍患者:3 名患者在体外受精期间胚胎发育不良,但原因不明,4 名患者被诊断为男性不育症,且先前表现出组蛋白变异。通过分离和纯化与组蛋白和鱼精蛋白结合的 DNA 来分析组蛋白和组蛋白修饰在全基因组上的位置。使用高通量测序分析组蛋白结合的 DNA 片段,最初和染色质免疫沉淀后均进行分析。鱼精蛋白结合的 DNA 片段与安捷伦芯片杂交。使用亚硫酸氢盐测序检查 DNA 甲基化。
与生育能力正常的男性不同,7 名不育男性中有 5 名男性在全基因组范围内存在非程序性(随机分布)的组蛋白保留。有趣的是,与总组蛋白池相比,不育男性的精子中 H3 赖氨酸 4 甲基化(H3K4me)或 H3 赖氨酸 27 甲基化(H3K27me)的定位与生育能力正常的男性高度相似。然而,在发育转录因子和某些印迹基因处保留的 H3K4me 或 H3K27me 量减少。最后,在一部分不育男性中,候选发育启动子和印迹基因座的甲基化状态发生了改变。
这项对不育男性精子中表观遗传标记物的全基因组分析首次表明,与生育能力正常的男性相比,不育男性的组成和表观遗传标记存在差异,尤其是在某些印迹和发育基因座处。尽管没有单个基因座显示出完整的染色质包装或 DNA 修饰变化,但数据表明整个基因组中存在适度的变化,并且可能对生育能力产生累积的不利影响。