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Intergenic bidirectional promoter and cooperative regulation of the IIx and IIb MHC genes in fast skeletal muscle

机译:基因间双向启动子和快速骨骼肌中IIx和IIb MHC基因的协同调控

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摘要

This study investigated the dynamic regulation of IIx-IIb MHC genes in the fast white medial gastrocnemius (WMG) muscle in response to intermittent resistance exercise training (RE), a model associated with a rapid shift from IIb to IIx expression (11). We investigated the effect of 4 days of RE on the transcriptional activity across the skeletal MHC gene locus in the WMG in female Sprague-Dawley rats. Our results show that RE resulted in significant shifts from IIb to IIx observed at both the pre-mRNA and mRNA levels. An antisense RNA (xII NAT) was detected in the intergenic (IG) region between IIx and IIb, extending across the entire IIx gene and into its promoter. The expression of the xII NAT was positively correlated with IIb pre-mRNA (R = +0.8), and negatively correlated with IIx pre-mRNA (R = −0.8). Transcription mapping of the IIx–IIb IG region revealed the generation of sense IIb and xII NATs from a single promoter region. This bidirectional promoter is highly conserved among species and contains several regulatory elements that may be implicated in its regulation. These results suggest that the IIx and the IIb genes are physically and functionally linked via the bidirectional promoter. In order for the IIx MHC gene to be regulated, a feedback mechanism from the IG xII NAT is needed. In conclusion, the IG bidirectional promoter generating antisense RNA appears to be essential for the coordinated regulation of the skeletal muscle MHC genes during dynamic phenotype shifts.
机译:这项研究调查了快白内侧腓肠肌(WMG)肌肉中IIx-IIb MHC基因对间歇性阻力运动训练(RE)的反应的动态调节,该模型与从IIb迅速转变为IIx表达相关(11)。我们调查了雌性Sprague-Dawley大鼠在WMG中4天的RE对跨骨骼MHC基因位点转录活性的影响。我们的结果表明,RE导致在前mRNA和mRNA水平上都从IIb明显转变为IIx。在IIx和IIb之间的基因间(IG)区域中检测到一个反义RNA(xII NAT),该区域遍及整个IIx基因并进入其启动子。 xII NAT的表达与IIb pre-mRNA正相关(R = +0.8),与IIx pre-mRNA负相关(R = -0.8)。 IIx–IIb IG区域的转录图谱揭示了单个启动子区域中有义IIb和xII NAT的产生。该双向启动子在物种中高度保守,并包含可能与其调控有关的几种调控元件。这些结果表明,IIx和IIb基因通过双向启动子在物理和功能上连接。为了调节IIx MHC基因,需要来自IG xII NAT的反馈机制。总之,IG双向启动子产生反义RNA似乎是动态表型转变过程中骨骼肌MHC基因的协调调控必不可少的。

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