Embryonic lethality of fortilin-null mutant mice by BMP-pathway overactivation.

Embryonic lethality of fortilin-null mutant mice by BMP-pathway overactivation.
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BMP 通路过度激活导致 fortilin 缺失突变小鼠的胚胎致死率。

DOI:
10.1016/j.bbagen.2009.01.012
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发表时间:
2009-05
影响因子:
3
通讯作者:
Fujise, Ken
Fujise, Ken
中科院分区:
生物学3区
文献类型:
--
作者:
Koide, Yuichi;Kiyota, Tomomi;Tonganunt, Moltira;Pinkaew, Decha;Liu, Zhihe;Kato, Yoichi;Hutadilok-Towatana, Nongporn;Phongdara, Amornrat;Fujise, Ken

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Fortilin negatively regulates apoptosis and is overexpressed in cancer. However, the role of fortilin in mammalian development is not clear. In order to evaluate the physiological role of fortilin in vivo, we performed a targeted disruption of the fortilin gene in mice. Fortilin+/− mice have the ability to survive and exhibit normal growth, while fortilin−/− mice are embryonically lethal around the 3.5 days post-coitum (dpc). Cultured blastocysts from fortilin+/− embryos undergo normal outgrowth to produce inner cell mass (ICM) and trophoblasts (TB), while ICM of fortilin−/− embryos either fails to outgrow or prematurely disintegrates. Mouse embryonic fibroblasts (MEF) derived from fortilin+/− embryos are more susceptible to noxious stimuli than are wild type embryos. It has been consistently shown in Xenopus embryos that the depletion of fortilin’s message severely compromises the formation of neural tissue, including the brain, while overexpression of fortilin induces the partial double body axis in embryos and is capable of blocking BMP4-induced transcription of Vent1, Vent2, and Msx1 genes. This suggests that fortilin is an inhibitor of the BMP pathway. Strikingly, when fortilin levels are reduced by siRNA, BMP4 causes MEF to undergo extensive DNA-fragmentation, while DNA fragmentation is minimal in the presence of fortilin. In addition, BMP4 induces more Msx2 in the absence of fortilin than in its presence. Furthermore, Msx2 overexpression causes MEF to undergo apoptotic cell death. We conclude that in early phase of development, fortilin functions as an inhibitor of the BMP pathway. The presence of fortilin in the very early stages of development is required for the survival of embryos. Abnormalities in the fortilin gene may be associated with early pregnancy loss.
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