MicroRNA expression in preimplantation mouse embryos from Ped gene positive compared to Ped gene negative mice

被引:25
作者
Byrne, Michael J. [1 ]
Warner, Carol M. [1 ]
机构
[1] Northeastern Univ, Dept Biol, Boston, MA 02115 USA
关键词
microRNA; miR-125; preimplantation embryos; Ped gene; Qa-2;
D O I
10.1007/s10815-008-9211-8
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Purpose The mouse preimplantation embryo development (Ped) gene product, Qa-2, influences the rate of preimplantation embryonic development and overall reproductive success. Here we investigated the expression pattern of two microRNAs, miR-125a and miR-125b, known to be involved in development in lower organisms, in preimplantation embryos from the two-cell, four-cell, eight-cell, morula, and blastocyst stages of development from the congenic B6.K1 (Ped negative) and B6.K2 (Ped positive) strains of mice. Method B6.K1 and B6.K2 congenic mice differ only in the absence (B6.K1) or presence (B6.K2) of the genes encoding Qa-2 protein. We analyzed the expression of miR-125a and miR-125b in B6.K1 and B6.K2 preimplantation embryos by using real-time PCR. Result We found no variability in miR-125b expression at any developmental stage in both strains. However, miR-125a expression increased during development in both strains and was ten times higher in Ped negative (B6.K1) embryos than in Ped positive (B6.K2) embryos by the blastocyst stage of development. Conclusion Our results show that the absence of the Ped gene profoundly affects the level of a miRNA (miR-125a) known to regulate early development. The implication is that miR-125a is likely involved in the regulation of timing of early development in mice.
引用
收藏
页码:205 / 214
页数:10
相关论文
共 48 条
[1]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[2]  
Boiso Irene, 2002, Reprod Biomed Online, V5, P328
[3]   MicroRNA functions [J].
Bushati, Natascha ;
Cohen, Stephen M. .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2007, 23 :175-205
[4]   Sequence and transcription of Qa-2-encoding genes in mouse lymphocytes and blastocysts [J].
Cai, WY ;
Cao, W ;
Wu, LZ ;
Exley, GE ;
Waneck, GL ;
Karger, BL ;
Warner, CM .
IMMUNOGENETICS, 1996, 45 (02) :97-107
[5]   Real-time quantification of microRNAs by stem-loop RT-PCR [J].
Chen, CF ;
Ridzon, DA ;
Broomer, AJ ;
Zhou, ZH ;
Lee, DH ;
Nguyen, JT ;
Barbisin, M ;
Xu, NL ;
Mahuvakar, VR ;
Andersen, MR ;
Lao, KQ ;
Livak, KJ ;
Guegler, KJ .
NUCLEIC ACIDS RESEARCH, 2005, 33 (20) :e179.1-e179.9
[6]   Crystal structure of HLA-G: A nonclassical MHC class I molecule expressed at the fetal-maternal interface [J].
Clements, CS ;
Kjer-Nielsen, L ;
Kostenko, L ;
Hoare, HL ;
Dunstone, MA ;
Moses, E ;
Freed, K ;
Brooks, AG ;
Rossjohn, J ;
McCluskey, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (09) :3360-3365
[7]   Evidence that HLA-G is the functional homolog of mouse Qa-2, the Ped gene product [J].
Comiskey, M ;
Goldstein, CY ;
De Fazio, SR ;
Mammolenti, M ;
Newmark, JA ;
Warner, CM .
HUMAN IMMUNOLOGY, 2003, 64 (11) :999-1004
[8]   HLA-G is found in lipid rafts and can act as a signaling molecule [J].
Comiskey, Martina ;
Domino, Kenneth E. ;
Warner, Carol M. .
HUMAN IMMUNOLOGY, 2007, 68 (01) :1-11
[9]   Secretion of soluble HLA-G by day 3 human embryos associated with higher pregnancy and implantation rates: assay of culture media using a new ELISA kit [J].
Desai, Nina ;
Filipovits, Jessica ;
Goldfarb, James .
REPRODUCTIVE BIOMEDICINE ONLINE, 2006, 13 (02) :272-277
[10]   GENETICS AND EXPRESSION OF THE Q6 AND Q8 GENES - AN LTR-LIKE SEQUENCE IN THE 3' UNTRANSLATED REGION [J].
ELLIOTT, E ;
RATHBUN, D ;
RAMSINGH, A ;
GARBERI, J ;
FLAHERTY, L .
IMMUNOGENETICS, 1989, 29 (06) :371-379