GRIM-19在小鼠植入前胚胎中的表达及其作用

崔文娟,邓晓惠,晁岚*,沈彦军,杨芳,冯文娟,徐静,陈红蕾

解剖学报 ›› 2013, Vol. 44 ›› Issue (1) : 97-101.

欢迎访问《解剖学报》官方网站!今天是 English
解剖学报 ›› 2013, Vol. 44 ›› Issue (1) : 97-101. DOI: 10.3969/j.issn.0529-1356.2013.01.019
组织学胚胎学发育生物学

GRIM-19在小鼠植入前胚胎中的表达及其作用

  • 崔文娟,邓晓惠,晁岚*,沈彦军,杨芳,冯文娟,徐静,陈红蕾
作者信息 +

Expression of GRIM-19 and its effects in preimplantation embryo of mice

  • CUI Wen-juan,DENG Xiao-hui,CHAO Lan*,SHEN Yan-jun,YANG Fang,FENG Wen-juan,XU Jing, CHEN Hong-lei 
Author information +
文章历史 +

摘要

目的 通过研究干扰素/维甲酸联合应用诱导细胞凋亡相关基因 (GRIM-19)在小鼠植入前胚胎中的表达及其与胚胎质量之间的相关性,探讨GRIM-19在小鼠植入前胚胎发育中的作用。方法 采用实时定量PCR,检测小鼠植入前胚胎(2-细胞期、4-细胞期、8-细胞期、桑葚胚和囊胚)中GRIM-19 mRNA水平 (n =16);将小鼠8细胞期胚胎按卵裂球大小、形态、透明带、胞质碎片分为优胚组和非优胚组,分别检测两组胚胎GRIM-19 mRNA水平,并分析其相关性 (n =13);制作假孕鼠(23只),并随机分为A组(12只)和B组(11只),采用移植器将优质和非优质8-细胞期胚胎移入假孕鼠的子宫内,观察两组雌鼠妊娠率及产仔率。结果 GRIM-19在小鼠植入前各期胚胎中均有表达,其mRNA水平从2-细胞期逐渐增高,至8-细胞期达高峰,随后呈下降趋势。优质8-细胞胚胎的GRIM-19 mRNA水平明显高于非优胚组(P <0.05)。两组8-细胞胚胎移植后,A组雌鼠妊娠率及产仔率显著高于B组雌鼠(P<0.05)。 结论 小鼠植入前胚胎中GRIM-19的表达量随发育时程的改变而变化,且与胚胎质量密切相关。

Abstract

Objective To study the expression of gene associated with retinoid-interferon-induced mortality-19(GRIM-19) and its correlation with the embryo quality, and to explore the effect of GRIM-19 in the development of preimplantation embryo of mice. Methods The expression of GRIM-19 in 2-cell, 4-cell, 8-cell, morula and blastocyst of mice preimplantation embryo was detected by using real-time PCR (n =16). Eight-cell embryos were divided into two groups: good quality embryos and bad quality embryos, according to their size, the pellucid zone and the debris of neoplasm. The different levels of embryos were detected (n=13). The expression of GRIM-19 in different groups were analyzed statistically. Results GRIM-19 expressed in every stage of preimplantation embryo of mice. The results of real-time PCR showed a gradually increase of GRIM-19 expression from 2-cell to 8-cell, and the expression then decreased progressively. In 8-cell embryo, mRNA expression of GRIM-19 in good quality embryos was significantly higher than that in bad quality embryos (P <0.05).Conclusion The expression of GRIM-19 in mouse preimplantation embryos is changed with the progress in development. GRIM-19 may reflect the potentiality of embryo development.

关键词

干扰素/维甲酸联合应用诱导细胞凋亡相关基因 / 植入前胚胎 / 线粒体 / 实时定量PCR / 小鼠

Key words

Gene associated with retinoid-interferon-induced mortality-19 / Preimplantation embryo / Mitochondria / Real-time PCR / Mouse

引用本文

导出引用
崔文娟,邓晓惠,晁岚*,沈彦军,杨芳,冯文娟,徐静,陈红蕾. GRIM-19在小鼠植入前胚胎中的表达及其作用[J]. 解剖学报. 2013, 44(1): 97-101 https://doi.org/10.3969/j.issn.0529-1356.2013.01.019
CUI Wen-juan,DENG Xiao-hui,CHAO Lan*,SHEN Yan-jun,YANG Fang,FENG Wen-juan,XU Jing, CHEN Hong-lei . Expression of GRIM-19 and its effects in preimplantation embryo of mice[J]. Acta Anatomica Sinica. 2013, 44(1): 97-101 https://doi.org/10.3969/j.issn.0529-1356.2013.01.019

参考文献

1] Angell JE, Lindner DJ, Shapiro PS, et al. Identification of GRIM-19, a novel cell death-regulatory gene induced by the interferon-beta and retinoic acid combination, using a genetic approach[J]. J Biol Chem, 2000, 275(43):33416-33426.

2]Chidambaram NV, Angell JE, Ling W, et al. Chromosomal localization of human GRIM-19, a novel IFN-beta and retinoic acid-activated regulator of cell death[J]. J Interferon Cytokine Res, 2000, 20(7):661-665.
3]Kalvakolanu DV. The GRIMs: a new interface between cell death regulation and interferon/retinoid induced growth suppression[J]. Cytokine Growth Factor Rev, 2004, 15(2-3):169-194.
4]Crabtree GR,Olson EN. NFAT signaling: choreographing the social lives of cells[J]. Cell, 2002, 109(Suppl):S67-79.
5]Dumollard R, Marangos P, Fitzharris G, et al. Sperm-triggered [Ca 2+ ] oscillations and Ca 2+ homeostasis in the mouse egg have an absolute requirement for mitochondrial ATP production[J]. Development, 2004, 131(13):3057-3067.
6]Graef IA, Chen F, Chen L, et al. Signals transduced by Ca( 2+ )/calcineurin and NFATc3/c4 pattern the developing vasculature[J]. Cell, 2001, 105(7):863-875.[7]Larsson NG, Wang J, Wilhelmsson H, et al. Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice[J]. Nat Genet, 1998, 18(3):231-236.
8]Huang G, Lu H, Hao A, et al. GRIM-19, a cell death regulatory protein, is essential for assembly and function of mitochondrial complex I[J]. Mol Cell Biol, 2004, 24(19):8447-8456.
9]Chen Y, Yuen WH, Fu J, et al. The mitochondrial respiratory chain controls intracellular calcium signaling and NFAT activity essential for heart formation in Xenopus laevis[J]. Mol Cell Biol, 2007, 27(18):6420-6432.
10]Lu H, Cao X. GRIM-19 is essential for maintenance of mitochondrial membrane potential[J]. Mol Biol Cell, 2008, 19(5):1893-1902.
11]Hiendleder S, Wolf E. The mitochondrial genome in embryo technologies[J]. Reprod Domest Anim, 2003, 38(4):290-304.
12]Van Blerkom J, Davis P, Alexander S. A microscopic and biochemical study of fragmentation phenotypes in stage-appropriate human embryos[J]. Hum Reprod, 2001, 16(4): 719-729.
13]Wilding M, Dale B, Marino M, et al, Mitochondrial aggregation patterns and activity in human oocytes and preimplantation embryos[J]. Hum Reprod, 2001, 16(5): 909-917.

基金

国家自然科学基金(30901603),山东省优秀中青年科学家科研奖励基金(BS2009SW031),山东省人口和计划生育委员会科学技术研究项目(2009年第8号);省自然科学基金资助项目


Accesses

Citation

Detail

段落导航
相关文章

/