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Expression and localization of Nlrp4g in mouse preimplantation embryo

Published online by Cambridge University Press:  11 November 2014

Hui Peng
Affiliation:
College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou, Fujian, 350002, People's Republic of China.
Xiujiao Lin
Affiliation:
College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou, Fujian, 350002, People's Republic of China.
Wenhao Li
Affiliation:
College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou, Fujian, 350002, People's Republic of China.
Wenchang Zhang*
Affiliation:
College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou, Fujian, 350002, People's Republic of China.
*
All correspondence to: Wenchang Zhang. College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou, Fujian, 350002, People's Republic of China. Tel: +86 591 83758852. Fax: +86 591 83758565. e-mail: zwcfz1221@126.com

Summary

The Nlrp gene family contains 20 members and plays a pivotal role in the innate immune and reproductive systems in the mouse. During evolution, seven Nlrp4 gene copies (named from Nlrp4a to Nlrp4g). Nlrp4a–Nlrp4g have arisen that display specific or preferential ovarian expression patterns. However, the expression pattern and localization of Nlrp4g in mouse preimplantation embryo development are unknown. Here we report that Nlrp4g was highly expressed in mature oocytes and zygotes, then downregulated and not detected after the 2-cell embryo stage. NLRP4G protein remained present through the blastocyst stage and was mainly localized in the cytoplasm. Furthermore, overexpression of Nlrp4g in zygotes did not affect normal development in terms of the rate of blastocyst formation. These results provide the first evidence that NLRP4G is a maternal factor that may play essential role during zygotic genome activation in the mouse.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2014 

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References

Bertin, J. & DiStefano, P.S. (2000). The PYRIN domain: a novel motif found in apoptosis and inflammation proteins. Cell Death Diff. 7, 1273–4.CrossRefGoogle ScholarPubMed
Boyden, E.D. & Dietrich, W.F. (2006). Nalp1b controls mouse macrophage susceptibility to anthrax lethal toxin. Nat. Genet. 38, 240–4.Google Scholar
Bultman, S.J., Gebuhr, T.C., Pan, H., Svoboda, P., Schultz, R.M. & Magnuson, T. (2006). Maternal BRG1 regulates zygotic genome activation in the mouse. Genes Dev. 20, 1744–54.Google Scholar
Burns, K.H., Viveiros, M.M., Ren, Y., Wang, P., DeMayo, F.J., Frail, D.E., Eppig, J.J. & Matzuk, M.M. (2003). Roles of NPM2 in chromatin and nucleolar organization in oocytes and embryos. Science 300, 633–6.Google Scholar
Dade, S., Callebaut, I., Paillisson, A., Bontoux, M., Dalbies-Tran, R. & Monget, P. (2004). In silico identification and structural features of six new genes similar to MATER specifically expressed in the oocyte. Biochem. Biophys. Res. Commun. 324, 547–53.CrossRefGoogle ScholarPubMed
Guarda, G., Dostert, C., Staehli, F., Cabalzar, K., Castillo, R., Tardivel, A., Schneider, P. & Tschopp, J. (2009). T cells dampen innate immune responses through inhibition of NLRP1 and NLRP3 inflammasomes. Nature 460, 269–73.CrossRefGoogle ScholarPubMed
Hamatani, T., Falco, G., Carter, M.G., Akutsu, H., Stagg, C.A., Sharov, A.A., Dudekula, D.B., Van Buren, V. & Ko, M.S. (2004). Age-associated alteration of gene expression patterns in mouse oocytes. Hum. Mol. Genet. 13, 2263–78.Google Scholar
Kobe, B. & Kajava, A.V. (2001). The leucine-rich repeat as a protein recognition motif. Curr. Opin. Struct. Biol. 11, 725–32.Google Scholar
Latham, K.E. (1999). Mechanisms and control of embryonic genome activation in mammalian embryos. Int. Rev. Cytol. 193, 71124.CrossRefGoogle ScholarPubMed
Lawitts, J.A. & Biggers, J.D. (1991). Optimization of mouse embryo culture media using simplex methods. J. Reprod. Fertil. 91, 543–56.CrossRefGoogle ScholarPubMed
Lawitts, J.A. & Biggers, J.D. (1993). Culture of preimplantation embryos. Methods Enzymol. 225, 153–64.CrossRefGoogle ScholarPubMed
Ma, J., Zeng, F., Schultz, R.M. & Tseng, H. (2006). Basonuclin: a novel mammalian maternal-effect gene. Development 133, 2053–62.Google Scholar
Nakahira, K., Haspel, J.A., Rathinam, V.A., Lee, S.J., Dolinay, T., Lam, H.C., Englert, J.A., Rabinovitch, M., Cernadas, M., Kim, H.P., Fitzgerald, K.A., Ryter, S.W. & Choi, A.M. (2011). Autophagy proteins regulate innate immune responses by inhibiting the release of mitochondrial DNA mediated by the NALP3 inflammasome. Nat. Immunol. 12, 222–30.CrossRefGoogle ScholarPubMed
Payer, B., Saitou, M., Barton, S.C., Thresher, R., Dixon, J.P., Zahn, D., Colledge, W.H., Carlton, M.B., Nakano, T. & Surani, M.A. (2003). Stella is a maternal effect gene required for normal early development in mice. Curr. Biol. 13, 2110–7.Google Scholar
Peng, H., Chang, B., Lu, C., Su, J., Wu, Y., Lv, P., Wang, Y., Liu, J., Zhang, B., Quan, F., Guo, Z. & Zhang, Y. (2012). Nlrp2, a maternal effect gene required for early embryonic development in the mouse. PLoS One 7, e30344.CrossRefGoogle ScholarPubMed
Peng, H., Zhuang, Y., Wu, X., Li, H., Hong, Z., Zhang, X., Lin, X. & Zhang, W. (2013). Expression analysis of Nlrp4a–Nlrp4f during mouse development. J. Anim. Vet. Adv. 12, 754–9.Google Scholar
Peng, H., Zhang, W., Xiao, T. & Zhang, Y. (2014a). Expression patterns of Nlrp9a, Nlrp9b and Nlrp9c during mouse development. Biologia 69, 107–12.Google Scholar
Peng, H., Zhang, W., Xiao, T. & Zhang, Y. (2014b). Nlrp4g is an oocyte-specific gene but is not required for oocyte maturation in the mouse. Reprod. Fertil. Dev. 26, 758–68.Google Scholar
Tian, X., Pascal, G. & Monget, P. (2009). Evolution and functional divergence of NLRP genes in mammalian reproductive systems. BMC Evol. Biol. 9, 202.Google Scholar
Ting, J.P., Lovering, R.C., Alnemri, E.S., Bertin, J., Boss, J.M., Davis, B.K., Flavell, R.A., Girardin, S.E., Godzik, A., Harton, J.A., Hoffman, H.M., Hugot, J.P., Inohara, N., Mackenzie, A., Maltais, L.J., Nunez, G., Ogura, Y., Otten, L.A., Philpott, D., Reed, J.C., Reith, W., Schreiber, S., Steimle, V. & Ward, P.A. (2008). The NLR gene family: a standard nomenclature. Immunity 28, 285–7.CrossRefGoogle Scholar
Tong, Z.B., Gold, L., Pfeifer, K.E., Dorward, H., Lee, E., Bondy, C.A., Dean, J. & Nelson, L.M. (2000). Mater, a maternal effect gene required for early embryonic development in mice. Nat. Genet. 26, 267–8.Google Scholar
Tong, Z.B., Gold, L., De Pol, A., Vanevski, K., Dorward, H., Sena, P., Palumbo, C., Bondy, C.A. & Nelson, L.M. (2004). Developmental expression and subcellular localization of mouse MATER, an oocyte-specific protein essential for early development. Endocrinology 145, 1427–34.Google Scholar
Wu, X., Viveiros, M.M., Eppig, J.J., Bai, Y., Fitzpatrick, S.L. & Matzuk, M.M. (2003). Zygote arrest 1 (Zar1) is a novel maternal-effect gene critical for the oocyte-to-embryo transition. Nat. Genet. 33, 187–91.Google Scholar
Yoshikawa, T., Piao, Y., Zhong, J., Matoba, R., Carter, M.G., Wang, Y., Goldberg, I. & Ko, M.S. (2006). High-throughput screen for genes predominantly expressed in the ICM of mouse blastocysts by whole mount in situ hybridization. Gene Expr. Patterns 6, 213–24.CrossRefGoogle ScholarPubMed
Zheng, P. & Dean, J. (2009). Role of Filia, a maternal effect gene, in maintaining euploidy during cleavage-stage mouse embryogenesis. Proc. Natl. Acad. Sci. USA 106, 7473–8.Google Scholar