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Regulation of compaction initiation in mouse embryo

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  • Department of Histology and Embryology, Harbin Medical University, Harbin 150081, China

Received date: 2009-08-24

  Revised date: 2009-10-02

  Online published: 2009-12-10

Abstract

Developmental events in preimplantation mouse embryos include the first cleavage, the activation of the embryonic genome, the compaction of the blastomeres to form morula (MO), and the formation of the blastocyst (BL). Compaction, the first cell differentiation event in mammalian development, occurs at the late eight-cell stage in the mouse and may be described in terms of some types of morphological change, which involve reorganization within a cell and intercellular reorganization. Surface microvilli became restricted to a few basal sites and to an externally facing (apical) pole. Prior to compaction, the blastomeres are spherical and lack specialized intercellular junctions. During compaction, the cells were flattened against one another, thus maximizing intercellular contact and obscuring intercellular boundaries. It is believed that the events of compaction have an important influence on the processes involved in blastocyst formation, namely the initiation of inner cell mass and trophectoderm differentiation. The inner cell mass will form the future embryo proper, whereas the trophectoderm cells will form only extraembryonic tissues. Compaction is initiated by E-cadherin mediated cell adhesion, which is regulated post-translationally via protein kinase C. With E-cadherin knock-out, maternal E-cadherin is able to mediate the compaction process at the morula stage. Initial adhesion is mediated by homophilic interactions between E-cadherin extracellular domains.In this review, we attempted to describe this process in detail.

Cite this article

LI Chao-Bei, HU Li-Li, WANG Zhen-Dong, ZHONG Chu-Qi, LEI Lei . Regulation of compaction initiation in mouse embryo[J]. Hereditas(Beijing), 2009 , 31(12) : 1177 -1184 . DOI: 10.3724/SP.J.1005.2009.01177

References

[1] Cui XS, Li XY, Shen XH, Bae YJ, Kang JJ, Kim NH. Transcription profile in mouse four-cell, morula, and blastocyst: genes implicated in compaction and blastocoel formation. Mol Repord Dev, 2007, 74(2): 133–143. [2] Ducibella T, Ukena T, Karnovsky M, Anderson E. Changes in cell surface and cortical cytoplasmic organiza-tion during early embryogenesis in the preimplantation mouse embryo. J Cell Biol, 1977, 74(1): 153–167. [3] Pratt HP, Ziomek CA, Reeve WJ. Compaction of the mouse embryo: an analysis of its components. J Embryol Exp Morphol, 1982, 70: 113–132. [4] Ohsugi M, Hwang SY, Butz S, Knowles BB, Solter D, Kemler R. Expression and cell membrane localization of catenins during mouse preimplantation development. Dev Dyn, 1996, 206(4): 391–402. [5] Plusa B, Frankenberg S, Chalmers A, Hadjantonakis AK, Moore CA, Papalopulu N, Papaioannou VE, Glover DM, Zernicka-Goetz M. Downregulation of Par3 and aPKC function directs cells towards the ICM in the preimplanta-tion mouse embryo. J Cell Sci, 2005, 118(Pt3): 505–515. [6] Violette MI, Madan P, Watson AJ. Na+/K+-ATPase regu-lates tight junction formation and function during mouse preimplantation development. Dev Biol, 2006, 289(2): 406–419. [7] Houghton FD. Role of gap junctions during early embryo development. Reproduction, 2005, 129(2): 129–135. [8] Balzac F, Avolio M, Degani S, Kaverina I, Torti M, Si-lengo L, Small JV, Retta SF. E-cadherin endocytosis regu-lates the activity of Rap1: a traffic light GTPase at the crossroads between cadherin and integrin function. J Cell Sci, 2005, 118(20): 4765–4783. [9] Koch AW, Manzur KL, Shan W. Structure-based models of cadherin-mediated cell adhesion: the evolution contin-ues. Cell Mol Life Sci, 2004, 61(15): 1884–1895. [10] Pokutta S, Drees F, Yamada S, Nelson WJ, Weis WI. Biochemical and structural analysis of alpha-catenin in cell-cell contacts. Biochem Soc Trans, 2008, 36(Pt2): 141–147. [11] Zhurinsky J, Shtutman M, Ben-Ze'ev A. Plakoglobin and b-catenin: protein interactions, regulation and biological roles. J Cell Sci, 2000, 113(Pt18): 3127–3139. [12] Piedra J, Martinez D, Castano J, Miravet S, Dunach M, de Herreros AG. Regulation of b-catenin structure and activ-ity by tyrosine phosphorylation. J Biol Chem, 2001, 276(23): 20436–20443. [13] Hinck L, Nathke IS, Papkoff J, Nelson WJ. Dynamics of cadherin/catenin complex formation: novel protein inter-actions and pathways of complex assembly. J Cell Biol, 1994, 125(6): 1327–1340. [14] Butz S, Kemler R. Distinct cadherin-catenin complexes in Ca2+-dependent cell-cell adhesion. FEBS Lett, 1994, 355(2): 195–200. [15] Drees F, Pokutta S, Yamada S, Nelson WJ, Weis WI. Al-pha-catenin is a molecular switch that binds E-cadherin- beta-catenin and regulates actin-filament assembly. Cell, 2005, 123(5): 903–915. [16] Pokutta S, Drees F, Takai Y, Nelson WJ, Weis WI. Bio-chemical and structural definition of the l-afadin- and ac-tin-binding sites of alpha-catenin. J Biol Chem, 2002, 277(21): 18868–18874. [17] Goyal RK, Lin P, Kanungo J, Payne AS, Muslin AJ, Longmore GD. Ajuba, a novel LIM protein, interacts with Grb2, augments mitogen-activated protein kinase activity in fibroblasts, and promotes meiotic maturation of Xenopus oocytes in a Grb2- and Ras-dependent manner. Mol Cell Biol, 1999, 19(6): 4379–4389. [18] Weis WI, Nelson WJ. Re-solving the cadherin-catenin-actin conundrum. J Biol Chem, 2006, 281(47): 35593–35597. [19] Yamada S, Nelson WJ. Localized zones of Rho and Rac activities drive initiation and expansion of epithelial cell-cell adhesion. J Cell Biol, 2007, 178(3): 517–527. [20] Halet G, Viard P, Carroll J. Constitutive PtdIns (3,4,5) P3 synthesis promotes the development and survival of early mammalian embryos. Development, 2008, 135(3): 425–429. [21] Vestweber D, Gossler A, Boller K, Kemler R. Expression and distribution of cell adhesion molecule uvomorulin in mo

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