Single-Cell-Resolution Imaging of the Impact of Notch Signaling and Mitosis on Segmentation Clock Dynamics

被引:118
作者
Delaune, Emilie A. [2 ]
Francois, Paul [1 ]
Shih, Nathan P. [2 ]
Amacher, Sharon L. [2 ]
机构
[1] McGill Univ, Dept Phys, Montreal, PQ H3A 2T8, Canada
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
PRESOMITIC MESODERM; VERTEBRATE SEGMENTATION; OSCILLATORY EXPRESSION; GENE-EXPRESSION; EMBRYONIC-DEVELOPMENT; ZEBRAFISH; HER1; ANTERIOR; PROTEIN; HES7;
D O I
10.1016/j.devcel.2012.09.009
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Vertebrate body segmentation is controlled by the segmentation clock, a molecular oscillator involving transcriptional oscillations of cyclic genes in presomitic mesoderm cells. The rapid and highly dynamic nature of this oscillating system has proved challenging for study at the single-cell level. We achieved visualization of clock activity with a cellular level of resolution in living embryos, allowing direct comparison of oscillations in neighbor cells. We provide direct evidence that presomitic mesoderm cells oscillate asynchronously in zebrafish Notch pathway mutants. By tracking oscillations in mitotic cells, we reveal that a robust cell-autonomous, Notch-independent mechanism resumes oscillations after mitosis. Finally, we find that cells preferentially divide at a certain oscillation phase, likely reducing the noise generated by cell division in cell synchrony and suggesting an intriguing relationship between the mitotic cycle and clock oscillation.
引用
收藏
页码:995 / 1005
页数:11
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