Mtango Namdori R, Latham Keith E
The Fels Institute for Cancer Research and Molecular Biology, Temple University, Philadelphia, Pennsylvania, USA.
Physiol Genomics. 2007 Sep 19;31(1):1-14. doi: 10.1152/physiolgenomics.00040.2007. Epub 2007 Jun 5.
Protein degradation via the ubiquitin-proteasome pathway (UPP) plays a key role in diverse aspects of cell physiology and development. In the early embryo, the UPP may play an important role in the transition from maternal to embryonic control of development. Disruptions in the UPP could thus compromise embryo developmental potential. Additionally, species-specific requirements may dictate diverse patterns of regulation of the UPP components. To investigate the expression of UPP components in a nonhuman primate embryo model, to compare expression between a primate and nonprimate species, and to determine whether disruption of this pathway may contribute to reduced developmental potential, we examined the expression of >50 mRNAs encoding UPP components in rhesus monkey oocytes and embryos. We compared this expression between the rhesus monkey and mouse embryo and between rhesus monkey oocytes and embryos of high, intermediate, and low developmental potential. We report here the temporal patterns of UPP gene expression in oocytes and during preimplantation development, including striking differences between the rhesus monkey and mouse. We also report significant differences in UPP gene expression correlating with oocyte and embryo developmental competence and associated with altered regulation of maternally inherited mRNAs encoding these proteins.
通过泛素-蛋白酶体途径(UPP)进行的蛋白质降解在细胞生理和发育的各个方面都起着关键作用。在早期胚胎中,UPP可能在从母体控制向胚胎控制发育的转变中发挥重要作用。因此,UPP的破坏可能会损害胚胎的发育潜力。此外,物种特异性需求可能决定了UPP组件的不同调控模式。为了研究UPP组件在非人类灵长类胚胎模型中的表达,比较灵长类和非灵长类物种之间的表达,并确定该途径的破坏是否可能导致发育潜力降低,我们检测了恒河猴卵母细胞和胚胎中50多种编码UPP组件的mRNA的表达。我们比较了恒河猴和小鼠胚胎之间以及恒河猴卵母细胞与高、中、低发育潜力胚胎之间的这种表达。我们在此报告了卵母细胞和植入前发育过程中UPP基因表达的时间模式,包括恒河猴和小鼠之间的显著差异。我们还报告了UPP基因表达的显著差异,这些差异与卵母细胞和胚胎的发育能力相关,并与编码这些蛋白质的母系遗传mRNA的调控改变有关。