Successful inactivation of endogenous Oct-3/4 and c-mos genes in mouse preimplantation embryos and oocytes using short interfering RNAs

被引:55
作者
Kim, MH
Yuan, XM
Okumura, S
Ishikawa, F
机构
[1] Tokyo Inst Technol, Grad Sch Biosci & Biotechnol, Dept Biol Informat, Lab Mol & Cellular Assembly,Midori Ku, Yokohama, Kanagawa 2268501, Japan
[2] Kyoto Univ, Grad Sch Biostudies, Lab Cell Cycle Regulat, Dept Gene Mechanisms, Kyoto, Japan
关键词
Mos; Oct-3/4; mouse; oocyte; embryo; RNA interference; short interfering RNA;
D O I
10.1016/S0006-291X(02)02070-3
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
Understanding oocyte maturation and early development in mammals is very important, especially because these cells serve as a source of materials useful in medical applications, such as ES cells. However, the limited availability of oocytes and embryos hampers the molecular dissection of the very early stage of mammalian development. Recently, the RNA interference technology has been acknowledged to be very effective and useful in diverse groups of cells, including mammalian cells. In this study, we examined whether short interfering RNAs (siRNAs) are applicable to mouse oocytes and preimplantation embryos, by targeting two genes, namely, Oct-3/4 and c-mos. siRNA injections successfully extinguished the production of these target genes. Moreover, the siRNA-injected oocytes and embryos showed phenotypes very similar to those exhibited by Oct-3/4- or Mos-knockout mice in previous studies. Accordingly, we concluded that siRNA is a useful tool in molecular studies on the early development of mouse. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:1372 / 1377
页数:6
相关论文
共 25 条
[1]   RNA interference: genetic wand and genetic watchdog [J].
Bosher, JM ;
Labouesse, M .
NATURE CELL BIOLOGY, 2000, 2 (02) :E31-E36
[2]   The Mos/mitogen-activated protein kinase (MAPK) pathway regulates the size and degradation of the first polar body in maturing mouse oocytes [J].
Choi, TS ;
Fukasawa, K ;
Zhou, RP ;
Tessarollo, L ;
Borror, K ;
Resau, J ;
VandeWoude, GF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (14) :7032-7035
[3]   DISRUPTION OF C-MOS CAUSES PARTHENOGENETIC DEVELOPMENT OF UNFERTILIZED MOUSE EGGS [J].
COLLEDGE, WH ;
CARLTON, MBL ;
UDY, GB ;
EVANS, MJ .
NATURE, 1994, 370 (6484) :65-68
[4]   Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells [J].
Elbashir, SM ;
Harborth, J ;
Lendeckel, W ;
Yalcin, A ;
Weber, K ;
Tuschl, T .
NATURE, 2001, 411 (6836) :494-498
[5]   Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans [J].
Fire, A ;
Xu, SQ ;
Montgomery, MK ;
Kostas, SA ;
Driver, SE ;
Mello, CC .
NATURE, 1998, 391 (6669) :806-811
[6]   PARTHENOGENETIC ACTIVATION OF OOCYTES IN C-MOS-DEFICIENT MICE [J].
HASHIMOTO, N ;
WATANABE, N ;
FURUTA, Y ;
TAMEMOTO, H ;
SAGATA, N ;
YOKOYAMA, M ;
OKAZAKI, K ;
NAGAYOSHI, M ;
TAKEDA, N ;
IKAWA, Y ;
AIZAWA, S .
NATURE, 1994, 370 (6484) :68-71
[7]  
JOHNSON LV, 1977, J EMBRYOL EXP MORPH, V40, P83
[8]  
LAWITTS JA, 1991, J REPROD FERTIL, V91, P543, DOI 10.1530/jrf.0.0910543
[9]   THE INTERFERON-INDUCED DOUBLE-STRANDED RNA-ACTIVATED PROTEIN-KINASE INDUCES APOPTOSIS [J].
LEE, SB ;
ESTEBAN, M .
VIROLOGY, 1994, 199 (02) :491-496
[10]   Delayed early embryonic lethality following disruption of the murine cyclin A2 gene [J].
Murphy, M ;
Stinnakre, MG ;
SenamaudBeaufort, C ;
Winston, NJ ;
Sweeney, C ;
Kubelka, M ;
Carrington, M ;
Brechot, C ;
SobczakThepot, J .
NATURE GENETICS, 1997, 15 (01) :83-86