1. Tong, Z.-B. and L.M. Nelson, A mouse gene encoding an oocyte antigen associated with autoimmune premature ovarian failure. Endocrinology, 1999. 140(8): p. 3720-3726. 2. Liang, L.-f., S.M. Soyal, and J. Dean, FIGalpha, a germ cell specific transcription factor involved in the coordinate expression of the zona pellucida genes. Development, 1997. 124(24): p. 4939-4947. 3. Capco, D.G., et al., Cytoskeletal sheets of mammalian eggs and embryos: A lattice-like network of intermediate filaments. Cell motility and the cytoskeleton, 1993. 24(2): p. 85-99. 4. Kim, K.-H. and K.-A. Lee, Maternal effect genes: Findings and effects on mouse embryo development. Clinical and experimental reproductive medicine, 2014. 41(2): p. 47-61. 5. Bettegowda, A., et al., JY-1, an oocyte-specific gene, regulates granulosa cell function and early embryonic development in cattle. Proceedings of the National Academy of Sciences, 2007. 104(45): p. 17602-17607. 6. Ohsugi, M., et al., Maternally derived FILIA-MATER complex localizes asymmetrically in cleavage-stage mouse embryos. Development, 2008. 135(2): p. 259-269. 7. Li, L., B. Baibakov, and J. Dean, A subcortical maternal complex essential for preimplantation mouse embryogenesis. Developmental cell, 2008. 15(3): p. 416-425. 8. Schultz, R.M., The molecular foundations of the maternal to zygotic transition in the preimplantation embryo. Human Reproduction Update, 2002. 8(4): p. 323-331. 9. Tong, Z.-B., L.M. Nelson, and J. Dean, Mater encodes a maternal protein in mice with a leucine-rich repeat domain homologous to porcine ribonuclease inhibitor. Mammalian Genome, 2000. 11(4): p. 281-287. 10. Tong, Z.-B., et al., Mater, a maternal effect gene required for early embryonic development in mice. Nature genetics, 2000. 26(3): p. 267-268. 11. Yurttas, P., et al., Role for PADI6 and the cytoplasmic lattices in ribosomal storage in oocytes and translational control in the early mouse embryo. Development, 2008. 135(15): p. 2627-2636. 12. Condic, M.L., The Role of Maternal-Effect Genes in Mammalian Development: Are Mammalian Embryos Really an Exception? Stem Cell Reviews and Reports, 2016: p. 1-9. 13. Kim, B., et al., Potential role for MATER in cytoplasmic lattice formation in murine oocytes. PloS one, 2010. 5(9): p. e12587. 14. Bebbere, D., et al., Expression pattern of zygote arrest 1 (ZAR1), maternal antigen that embryo requires (MATER), growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) genes in ovine oocytes and in vitro-produced preimplantation embryos. Reproduction, Fertility and Development, 2008. 20(8): p. 908-915. 15. Bebbere, D., et al., The subcortical maternal complex: multiple functions for one biological structure? Journal of Assisted Reproduction and Genetics, 2016: p. 1-8. 16. Lim, A.K. and B.B. Knowles, Controlling endogenous retroviruses and their chimeric transcripts during natural reprogramming in the oocyte. Journal of Infectious Diseases, 2015. 212(suppl 1): p. S47-S51. 17. Li, L., P. Zheng, and J. Dean, Maternal control of early mouse development. Development, 2010. 137(6): p. 859-870. 18. Kim, B., et al., The role of MATER in endoplasmic reticulum distribution and calcium homeostasis in mouse oocytes. Developmental biology, 2014. 386(2): p. 331-339. 19. Tashiro, F., et al., Maternal-effect gene Ces5/Ooep/Moep19/Floped is essential for oocyte cytoplasmic lattice formation and embryonic development at the maternal-zygotic stage transition. Genes to Cells, 2010. 15(8): p. 813-828. 20. Peng, H., et al., Knockdown of NLRP5 arrests early embryogenesis in sows. Animal Reproduction Science, 2015. 163: p. 151-156. 21. Yu, C., et al., BTG4 is a meiotic cell cycle-coupled maternal-zygotic-transition licensing factor in oocytes. Nature structural molecular biology, 2016. 23(5): p. 387-394. 22. Park, M.-W., et al., Associations among Sebox and other MEGs and its effects on early embryogenesis. PloS one, 2015. 10(2): p. e0115050. 23. Hu, J., et al., Insulin–transferrin–selenium (ITS) improves maturation of porcine oocytes in vitro. Zygote, 2011. 19(03): p. 191-197. 24. Duncan, F.E., et al., Transducin-Like Enhancer of Split-6 (TLE6) Is a Substrate of Protein Kinase A Activity During Mouse Oocyte Maturation 1. Biology of reproduction, 2014. 90(3): p. 1-12. 25. Alazami, A.M., et al., TLE6 mutation causes the earliest known human embryonic lethality. Genome biology, 2015. 16(1): p. 1. 26. Yan-dong, L.I., et al., Signaling Pathways Involving in Mammalian Oocyte Maturation: A Review. Journal of International Reproductive Health/Family Planning, 2015. 34(2). 27. Agarwal, M., P. Kumar, and S.J. Mathew, The Groucho/Transducin-ike enhancer of split protein family in animal development. IUBMB life, 2015. 67(7): p. 472-481. 28. Lu, Y.-q., X.-c. He, and P. Zheng, Decrease in expression of maternal effect gene Mater is associated with maternal ageing in mice. Molecular human reproduction, 2016. 22(4): p. 252-260. 29. van Beers, J.J.B.C., et al., Peptidylarginine deiminase expression and activity in PAD2 knock-out and PAD4-low mice. Biochimie, 2011. 95(2): p. 299-308. 30. Wright, P.W., et al., ePAD, an oocyte and early embryo-abundant peptidylarginine deiminase-like protein that localizes to egg cytoplasmic sheets. Developmental biology, 2003. 256(1): p. 74-89. 31. Zhu, K., et al., Identification of a human subcortical maternal complex. Molecular human reproduction, 2015. 21(4): p. 320-329. 32. Suzuki, A., et al., Decreased severity of experimental autoimmune arthritis in peptidylarginine deiminase type 4 knockout mice. BMC musculoskeletal disorders, 2016. 17(1): p. 1. 33. Esposito, G., et al., Peptidylarginine deiminase (PAD) 6 is essential for oocyte cytoskeletal sheet formation and female fertility. Molecular and cellular endocrinology, 2007. 273(1): p. 25-31. 34. Monti, M., et al., Developmental arrest and mouse antral not-surrounded nucleolus oocytes. Biology of reproduction, 2013. 88(1): p. 2. 35. Docherty, L.E., et al., Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans. Nature communications, 2015. 6. 36. Jaitin, D.A., et al., Massively parallel single-cell RNA-seq for marker-free decomposition of tissues into cell types. Science, 2014. 343(6172): p. 776-779. 37. Tang, F., et al., Tracing the derivation of embryonic stem cells from the inner cell mass by single-cell RNA-Seq analysis. Cell stem cell, 2014. 6(5): p. 468-478. 38. Deng, Q., et al., Single-cell RNA-seq reveals dynamic, random monoallelic gene expression in mammalian cells. Science, 2014. 343(6167): p. 193-196. 39. Yan, L., et al., Single-cell RNA-Seq profiling of human preimplantation embryos and embryonic stem cells. Nature structural molecular biology, 2013. 20(9): p. 1131-1139. 40. Islam, S., et al., Quantitative single-cell RNA-seq with unique molecular identifiers. Nature methods, 2014. 11(2): p. 163-166.
|