Hiltunen Anniina E, Vuolteenaho Reetta, Ronkainen Veli-Pekka, Miinalainen Ilkka, Uusimaa Johanna, Lehtonen Siri, Hinttala Reetta
Medical Research Center Oulu and PEDEGO Research Unit, University of Oulu and Oulu University Hospital, Oulu, Finland.
Biocenter Oulu, University of Oulu, Oulu, Finland.
Genesis. 2022 Mar;60(3):e23470. doi: 10.1002/dvg.23470. Epub 2022 Mar 8.
The loss of NHL repeat containing 2 (Nhlrc2) leads to early embryonic lethality in mice, but the exact timing is currently unknown. In this study, we determined the time of lethality for Nhlrc2 knockout (KO), C57BL/6NCrl-Nhlrc2 /Oulu, embryos and the in situ expression pattern of Nhlrc2 based on LacZ reporter gene expression during this period. Nhlrc2 KO preimplantation mouse embryos developed normally after in vitro fertilization. Embryonic stem (ES) cells established from KO blastocysts proliferated normally despite a complete loss of the NHLRC2 protein. Nhlrc2 KO embryos from timed matings implanted and were indistinguishable from their wildtype littermates on embryonic day (E) 6.5. On E7.5, Nhlrc2 KO embryo development was arrested, and on E8.5, only 6% of the genotyped embryos were homozygous for the Nhlrc2 allele. Nhlrc2 KO E8.5 embryos showed limited embryonic or extraembryonic tissue differentiation and remained at the cylinder stage. Nhlrc2 expression was ubiquitous but strongest in the epiblast/ectoderm and extraembryonic ectoderm on E6.5 and E7.5. NHLRC2 is essential for early postimplantation development, and its loss leads to failed gastrulation and amniotic folding in mice. Future studies on the evolutionarily conserved NHLRC2 will provide new insights into the molecular pathways involved in the early steps of postimplantation development.
含NHL重复序列2(Nhlrc2)的缺失会导致小鼠早期胚胎致死,但确切时间目前尚不清楚。在本研究中,我们确定了Nhlrc2基因敲除(KO)小鼠C57BL/6NCrl-Nhlrc2 /Oulu胚胎的致死时间,以及在此期间基于LacZ报告基因表达的Nhlrc2原位表达模式。Nhlrc2基因敲除的植入前小鼠胚胎在体外受精后发育正常。从基因敲除囊胚建立的胚胎干细胞(ES细胞)尽管NHLRC2蛋白完全缺失,但仍能正常增殖。定时交配得到的Nhlrc2基因敲除胚胎在胚胎第(E)6.5天植入,与野生型同窝仔没有区别。在E7.5时,Nhlrc2基因敲除胚胎的发育停止,在E8.5时,只有6%的基因分型胚胎为Nhlrc2等位基因纯合子。Nhlrc2基因敲除的E8.5胚胎显示出有限的胚胎或胚外组织分化,仍处于圆柱期。Nhlrc2在E6.5和E7.5时表达普遍,但在胚泡/外胚层和胚外外胚层中最强。NHLRC2对植入后早期发育至关重要,其缺失会导致小鼠原肠胚形成和羊膜折叠失败。未来对进化保守的NHLRC2的研究将为植入后发育早期步骤所涉及的分子途径提供新的见解。