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CF2转录因子参与Mef2 RNA水平、细胞核数量和肌纤维大小的调控。

CF2 transcription factor is involved in the regulation of Mef2 RNA levels, nuclei number and muscle fiber size.

作者信息

Arredondo Juan J, Vivar Jorge, Laine-Menéndez Sara, Martínez-Morentin Leticia, Cervera Margarita

机构信息

Departamento de Bioquímica, Instituto de Investigaciones Biomédicas "Alberto Sols" UAM-CSIC and Centro de Investigación Biomédica en Red (CIBERER), c/ Arzobispo Morcillo 4, Facultad de Medicina, Universidad Autónoma de Madrid, Madrid, Spain.

出版信息

PLoS One. 2017 Jun 15;12(6):e0179194. doi: 10.1371/journal.pone.0179194. eCollection 2017.

DOI:10.1371/journal.pone.0179194
PMID:28617826
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5472297/
Abstract

CF2 and Mef2 influence a variety of developmental muscle processes at distinct stages of development. Nevertheless, the exact nature of the CF2-Mef2 relationship and its effects on muscle building remain yet to be resolved. Here, we explored the regulatory role of CF2 in the Drosophila embryo muscle formation. To address this question and not having proper null CF2 mutants we exploited loss or gain of function strategies to study the contribution of CF2 to Mef2 transcription regulation and to muscle formation. Our data point to CF2 as a factor involved in the regulation of muscle final size and/or the number of nuclei present in each muscle. This function is independent of its role as a Mef2 collaborative factor in the transcriptional regulation of muscle-structural genes. Although Mef2 expression patterns do not change, reductions or increases in parallel in CF2 and Mef2 transcript abundance were observed in interfered and overexpressed CF2 embryos. Since CF2 expression variations yield altered Mef2 expression levels but with correct spatio-temporal Mef2 expression patterns, it can be concluded that only the mechanism controlling expression levels is de-regulated. Here, it is proposed that CF2 regulates Mef2 expression through a Feedforward Loop circuit.

摘要

CF2和Mef2在发育的不同阶段影响多种发育性肌肉过程。然而,CF2与Mef2关系的确切性质及其对肌肉生成的影响仍有待解决。在这里,我们探讨了CF2在果蝇胚胎肌肉形成中的调控作用。为了解决这个问题且没有合适的CF2无效突变体,我们利用功能丧失或功能获得策略来研究CF2对Mef2转录调控和肌肉形成的贡献。我们的数据表明CF2是参与调节肌肉最终大小和/或每条肌肉中细胞核数量的一个因子。该功能独立于其作为肌肉结构基因转录调控中Mef2协同因子的作用。尽管Mef2的表达模式没有变化,但在CF2受到干扰和过表达的胚胎中,观察到CF2和Mef2转录本丰度同时降低或增加。由于CF2表达变化导致Mef2表达水平改变,但Mef2的时空表达模式正确,因此可以得出结论,只有控制表达水平的机制失调。在此,我们提出CF2通过前馈环回路调节Mef2的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/d9056c7a5c18/pone.0179194.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/3c9db1630ab2/pone.0179194.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/90d75a36d3e3/pone.0179194.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/177dd8544750/pone.0179194.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/9a22ef5bd34a/pone.0179194.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/d392b088946c/pone.0179194.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/c543e5464e34/pone.0179194.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/d9056c7a5c18/pone.0179194.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/3c9db1630ab2/pone.0179194.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/90d75a36d3e3/pone.0179194.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/177dd8544750/pone.0179194.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/9a22ef5bd34a/pone.0179194.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/d392b088946c/pone.0179194.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/c543e5464e34/pone.0179194.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c85b/5472297/d9056c7a5c18/pone.0179194.g007.jpg

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