Mortlock Sally, McKinnon Brett, Montgomery Grant W
Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD, Australia.
Front Reprod Health. 2022 Jan 3;3:795464. doi: 10.3389/frph.2021.795464. eCollection 2021.
The endometrium is a complex and dynamic tissue essential for fertility and implicated in many reproductive disorders. The tissue consists of glandular epithelium and vascularised stroma and is unique because it is constantly shed and regrown with each menstrual cycle, generating up to 10 mm of new mucosa. Consequently, there are marked changes in cell composition and gene expression across the menstrual cycle. Recent evidence shows expression of many genes is influenced by genetic variation between individuals. We and others have reported evidence for genetic effects on hundreds of genes in endometrium. The genetic factors influencing endometrial gene expression are highly correlated with the genetic effects on expression in other reproductive (e.g., in uterus and ovary) and digestive tissues (e.g., salivary gland and stomach), supporting a shared genetic regulation of gene expression in biologically similar tissues. There is also increasing evidence for cell specific genetic effects for some genes. Sample size for studies in endometrium are modest and results from the larger studies of gene expression in blood report genetic effects for a much higher proportion of genes than currently reported for endometrium. There is also emerging evidence for the importance of genetic variation on RNA splicing. Gene mapping studies for common disease, including diseases associated with endometrium, show most variation maps to intergenic regulatory regions. It is likely that genetic risk factors for disease function through modifying the program of cell specific gene expression. The emerging evidence from our gene mapping studies coupled with tissue specific studies, and the GTEx, eQTLGen and EpiMap projects, show we need to expand our understanding of the complex regulation of gene expression. These data also help to link disease genetic risk factors to specific target genes. Combining our data on genetic regulation of gene expression in endometrium, and cell types within the endometrium with gene mapping data for endometriosis and related diseases is beginning to uncover the specific genes and pathways responsible for increased risk of these diseases.
子宫内膜是一种复杂且动态变化的组织,对生育至关重要,并与许多生殖系统疾病相关。该组织由腺上皮和血管化的基质组成,其独特之处在于它会在每个月经周期不断脱落并重新生长,生成多达10毫米的新黏膜。因此,在整个月经周期中,细胞组成和基因表达会发生显著变化。最近的证据表明,许多基因的表达受个体间遗传变异的影响。我们和其他人已经报告了子宫内膜中数百个基因存在遗传效应的证据。影响子宫内膜基因表达的遗传因素与对其他生殖组织(如子宫和卵巢)以及消化组织(如唾液腺和胃)中基因表达的遗传效应高度相关,这支持了在生物学上相似的组织中基因表达存在共享遗传调控的观点。对于某些基因,细胞特异性遗传效应的证据也在不断增加。子宫内膜研究的样本量适中,而血液中基因表达的更大规模研究报告的基因遗传效应比例比目前子宫内膜研究报告的要高得多。关于遗传变异对RNA剪接重要性的证据也在不断涌现。针对常见疾病(包括与子宫内膜相关的疾病)的基因定位研究表明,大多数变异定位于基因间调控区域。疾病的遗传风险因素可能通过改变细胞特异性基因表达程序来发挥作用。我们的基因定位研究以及组织特异性研究,再加上基因型-组织表达(GTEx)、表达数量性状基因座(eQTLGen)和表观基因组图谱(EpiMap)项目所提供的新证据表明,我们需要扩展对基因表达复杂调控的理解。这些数据还有助于将疾病遗传风险因素与特定靶基因联系起来。将我们关于子宫内膜中基因表达的遗传调控以及子宫内膜内细胞类型的数据与子宫内膜异位症及相关疾病的基因定位数据相结合,开始揭示导致这些疾病风险增加的特定基因和途径。