ARID1A, a component of SWI/SNF chromatin remodeling complexes, is required for porcine embryo development

被引:7
|
作者
Tseng, Yu-Chun [1 ]
Cabot, Birgit [1 ]
Cabot, Ryan A. [1 ]
机构
[1] Purdue Univ, Dept Anim Sci, 915 West State St, W Lafayette, IN 47907 USA
基金
美国国家卫生研究院;
关键词
BAF; BRG1; epigenetics; PIG EMBRYOGENESIS; IN-VITRO; BRG1; EXPRESSION; OOCYTES; FERTILIZATION; GROWTH; GENES;
D O I
10.1002/mrd.22924
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
Mammalian embryos undergo dramatic epigenetic remodeling that can have a profound impact on both gene transcription and overall embryo developmental competence. Members of the SWI/SNF (Switch/Sucrose non-fermentable) family of chromatin-remodeling complexes reposition nucleosomes and alter transcription factor accessibility. These large, multi-protein complexes possess an SNF2-type ATPase (either SMARCA4 or SMARCA2) as their core catalytic subunit, and are directed to specific loci by associated subunits. Little is known about the identity of specific SWI/SNF complexes that serve regulatory roles during cleavage development. ARID1A, one of the SWI/SNF complex subunits, can affect histone methylation in somatic cells; here, we determined the developmental requirements of ARID1A in porcine oocytes and embryos. We found ARID1A transcript levels were significantly reduced in 4-cell porcine embryos as compared to germinal vesicle-stage oocytes, suggesting that ARID1A would be required for porcine cleavage-stage development. Indeed, injecting in vitro-matured and fertilized porcine oocytes with double-stranded interfering RNAs that target ARID1A, and evaluating their phenotype after seven days, revealed that the depletion of ARID1A results in significantly fewer cells than their respective control groups (p<0.001).
引用
收藏
页码:1250 / 1256
页数:7
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