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Cell Cycle News & Views

Getting the broken blastomere out of development

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Pages 3247-3248 | Received 16 Sep 2013, Accepted 19 Sep 2013, Published online: 26 Sep 2013

Figures & data

Figure 1. The DNA damage response (DDR) of individual blastomere in early embryo. Laser microbeam is used to generate DNA breaks of a single blastomere by aiming at a specific region of the nucleus. DNA damages induce the activation of ATM, which phosphorylates H2AX and amplifies DNA damage signal. The active ATM further activates its downstream substrates, such as Chk2, the mediator of the DDR. Phosphorylated Chk2 causes a series of reactions and finally triggers apoptosis signals to the blastomere. The blastomere ceases cleavage and cannot incorporate into compacted morula.

Figure 1. The DNA damage response (DDR) of individual blastomere in early embryo. Laser microbeam is used to generate DNA breaks of a single blastomere by aiming at a specific region of the nucleus. DNA damages induce the activation of ATM, which phosphorylates H2AX and amplifies DNA damage signal. The active ATM further activates its downstream substrates, such as Chk2, the mediator of the DDR. Phosphorylated Chk2 causes a series of reactions and finally triggers apoptosis signals to the blastomere. The blastomere ceases cleavage and cannot incorporate into compacted morula.