Department of Biomedicine, Aarhus University, Aarhus, Denmark.
Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
Biol Reprod. 2019 Aug 1;101(2):284-296. doi: 10.1093/biolre/ioz098.
Nucleotide-binding oligomerization domain (NOD)-like receptors with a pyrin domain (PYD), NLRPs, are pattern recognition receptors, well recognized for their important roles in innate immunity and apoptosis. However, several NLRPs have received attention for their new, specialized roles as maternally contributed genes important in reproduction and embryo development. Several NLRPs have been shown to be specifically expressed in oocytes and preimplantation embryos. Interestingly, and in line with divergent functions, NLRP genes reveal a complex evolutionary divergence. The most pronounced difference is the human-specific NLRP7 gene, not identified in rodents. However, mouse models have been extensively used to study maternally contributed NLRPs. The NLRP2 and NLRP5 proteins are components of the subcortical maternal complex (SCMC), which was recently identified as essential for mouse preimplantation development. The SCMC integrates multiple proteins, including KHDC3L, NLRP5, TLE6, OOEP, NLRP2, and PADI6. The NLRP5 (also known as MATER) has been extensively studied. In humans, inactivating variants in specific NLRP genes in the mother are associated with distinct phenotypes in the offspring, such as biparental hydatidiform moles (BiHMs) and preterm birth. Maternal-effect recessive mutations in KHDC3L and NLRP5 (and NLRP7) are associated with reduced reproductive outcomes, BiHM, and broad multilocus imprinting perturbations. The precise mechanisms of NLRPs are unknown, but research strongly indicates their pivotal roles in the establishment of genomic imprints and post-zygotic methylation maintenance, among other processes. Challenges for the future include translations of findings from the mouse model into human contexts and implementation in therapies and clinical fertility management.
核苷酸结合寡聚化结构域 (NOD)-样受体含有一个吡咯并嘧啶结构域 (PYD),NLRPs 是模式识别受体,它们在先天免疫和细胞凋亡中发挥着重要作用,这一点得到了广泛的认可。然而,有几个 NLRP 因其作为在生殖和胚胎发育中具有重要作用的母源性基因的新的、特殊作用而受到关注。已经发现几个 NLRP 专门在卵母细胞和着床前胚胎中表达。有趣的是,与不同的功能一致,NLRP 基因显示出复杂的进化分歧。最明显的差异是人类特有的 NLRP7 基因,在啮齿动物中没有发现。然而,已经广泛使用小鼠模型来研究母源性 NLRP。NLRP2 和 NLRP5 蛋白是亚皮质母性复合物 (SCMC) 的组成部分,该复合物最近被确定对小鼠着床前发育至关重要。SCMC 整合了多种蛋白质,包括 KHDC3L、NLRP5、TLE6、OOEP、NLRP2 和 PADI6。NLRP5(也称为 MATER)已被广泛研究。在人类中,母亲体内特定 NLRP 基因的失活变异与后代的独特表型有关,例如双亲性葡萄胎 (BiHMs) 和早产。KHDC3L 和 NLRP5(和 NLRP7)的母源性隐性突变与生殖结局降低、BiHM 和广泛的多基因印记扰动有关。NLRPs 的精确机制尚不清楚,但研究强烈表明它们在基因组印记的建立和合子后甲基化维持等过程中发挥着关键作用。未来的挑战包括将小鼠模型的研究结果转化为人类背景,并将其应用于治疗和临床生育管理。