Timing of developmental events in the early mouse embryo

被引:101
|
作者
Kojima, Yoji [1 ]
Tam, Oliver H. [2 ]
Tam, Patrick P. L. [3 ,4 ]
机构
[1] Kyoto Univ, Inst Integrated Cell Mat Sci, Kyoto 6068501, Japan
[2] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[3] Univ Sydney, Childrens Med Res Inst, Embryol Unit, Westmead, NSW 2145, Australia
[4] Univ Sydney, Sydney Med Sch, Westmead, NSW 2145, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
Mouse embryo; Morphogenesis; Gastrulation; Transcriptome; Timing mechanism; EARLY XENOPUS-EMBRYOS; INNER CELL MASS; SIZE REGULATION; PRIMITIVE ENDODERM; PLURIPOTENT CELLS; STEM-CELLS; IN-VITRO; BLASTOCYST; AXIS; EPIBLAST;
D O I
10.1016/j.semcdb.2014.06.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The timing of developmental events during early mouse development has been investigated in embryos that have been subject to experimental manipulation of cell number and tissue mass. These phenomenological studies revealed that the timing of preimplantation events, such as compaction, formation of blastocyst cavity and lineage allocation is correlated with the rounds of cleavage division or DNA replication of the blastomeres. Timing of postimplantation processes, such as formation of proamniotic cavity and onset of gastrulation is sensitive to cell number and probably the tissue mass, which may be measured by a mechanosensory signaling mechanism. Developmental changes in these two physical attributes are correlated with the cell proliferative activity and the growth trajectory of the whole embryo prior to the transit to organogenesis. During organogenesis, timing of morphogenesis appears to be regulated by individual devices that could be uncoupled during compensatory growth. Insights of the timing mechanism may be gleaned from the analysis of genomic activity associated with the transition through developmental milestones. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:65 / 75
页数:11
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