Hicks Jessica E, Petters Robert M, Sommer Jeffrey R, Farin Charlotte E
Department of Animal Science, College of Agriculture and Life Sciences, North Carolina State University - EUA.
JBRA Assist Reprod. 2014 Sep 27;18(3):69-75. doi: 10.5935/1518-0557.20140010.
A series of experiments were performed to define the time required for transcription initiation during FSH-induced maturation in bovine COCs, determine the pattern of expression for candidate mRNAs during GVBD, and use RNAi to determine their potential role in GVBD by examining whether candidate-specific siRNA can reduce mRNA expression in bovine COCs and affect the occurrence of GVBD.
Transcription required for GVBD in bovine COC occurred as early as 30 min after culture initiation. Expression of Nr4A1 mRNA increased (P <0.05) at 30 min after culture initiation, consistent with the time of transcription initiation required for GVBD. Expression of Egr1 mRNA did not differ during culture. Expression of Nr4A1 mRNA was decreased (P <0.05) in COC cultured with 50nM siNr4A1 or with 120 µM of the transcriptional inhibitor DRB compared to controls. The proportion of COC undergoing GVBD at 9 hr of culture in FSH and non-specific siRNA (siNS) treatment groups did not differ. However, fewer (P <0.05) COC underwent GVBD at 9 hr of culture when in the presence of DRB or 50nM siNr4A1 compared to controls.
these data support a role for Nr4A1 in regulating FSH-mediated and transcription-dependent GVBD in bovine COC cultured in vitro.
1)进一步明确牛卵丘-卵母细胞复合体(COC)中转录起始所需的时间进程;2)确定Nr4A1和Egr1 mRNA在牛COC中的表达模式;3)使用小干扰RNA(siRNA)降低Nr4A1 mRNA表达,以确定其对生发泡破裂(GVBD)的影响。
进行了一系列实验,以确定牛COC在促卵泡激素(FSH)诱导成熟过程中转录起始所需的时间,确定生发泡破裂期间候选mRNA的表达模式,并通过检查候选特异性siRNA是否能降低牛COC中的mRNA表达并影响GVBD的发生,利用RNA干扰来确定它们在GVBD中的潜在作用。
牛COC中GVBD所需的转录早在培养开始后30分钟就发生了。培养开始后30分钟,Nr4A1 mRNA的表达增加(P<0.05),这与GVBD所需的转录起始时间一致。培养期间Egr1 mRNA的表达没有差异。与对照组相比,用50nM siNr4A1或120µM转录抑制剂DRB培养的COC中,Nr4A1 mRNA的表达降低(P<0.05)。FSH和非特异性siRNA(siNS)处理组在培养9小时时发生GVBD的COC比例没有差异。然而,与对照组相比,在存在DRB或50nM siNr4A1的情况下,培养9小时时发生GVBD的COC较少(P<0.05)。
这些数据支持Nr4A1在体外培养的牛COC中调节FSH介导的和转录依赖性GVBD中的作用。