Subcellular localization of presenilins during mouse preimplantation development

被引:16
|
作者
Jeong, SJ
Kim, HS
Chang, KA
Geum, DH
Park, CH
Seo, JH
Rah, JC
Lee, JH
Choi, SH
Lee, SG
Kim, K
Suh, YH
机构
[1] Seoul Natl Univ, Coll Med, Dept Pharmacol, Chongno Gu, Seoul 110799, South Korea
[2] Seoul Natl Univ, Med Res Ctr, Neurosci Res Inst, Seoul 110799, South Korea
[3] Korea Natl Inst Hlth, Biomed Brain Res Ctr, Seoul 110799, South Korea
[4] Seoul Natl Univ, Coll Nat Sci, Dept Mol Biol, Seoul 151742, South Korea
[5] Seoul Natl Univ, Coll Nat Sci, Cell Differentiat Res Ctr, Seoul 151742, South Korea
来源
FASEB JOURNAL | 2000年 / 14卷 / 14期
关键词
preimplantation embryos; nucleus; centrosome-kinetochore microtubule; cell division;
D O I
10.1096/fj.99-1068com
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The genes defective hi familial Alzheimer's disease encode the proteins presenilin 1 and 2 (PS1 and 2). Expression of presenilins (PSs) and their proteolytic processing are regulated during neuronal development. Even though these proteins are detected and regulated mainly in Golgi and endoplasmic reticulum, their subcellular distribution during the development is not known. The present study aimed to investigate the localization of PSs and their role during early developmental stage using mouse embryo model. At preimplantation stage, PSs were detected not only in cytoplasm, but also in the nucleus from oocyte to 2.5 dpc (day postcoitum), then disappeared in the nucleus at blastocyst stage (3.5 dpc). Antisense against PS1 and PS2 decreased the transition to blastocyst stage, whereas each antisense alone had no effect. Treatment with lactacystin (26S proteosome inhibitor), which arrest cell cycle at M phase, redistributed PSs into centrosome-kinetochore microtubule. PS2 overexpression in HEK 293 cell arrested cell cycle at S phase. These data suggest that PSs play key roles in cell division and differentiation during early development.
引用
收藏
页码:2171 / 2176
页数:6
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