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骨骼肌分化的 microRNA-mRNA 谱及其与先天性肌强直性营养不良的相关性。

microRNA-mRNA Profile of Skeletal Muscle Differentiation and Relevance to Congenital Myotonic Dystrophy.

机构信息

Division of Newborn Medicine, Boston Children's Hospital, Boston, MA 02115, USA.

Department of Pediatrics, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Int J Mol Sci. 2021 Mar 7;22(5):2692. doi: 10.3390/ijms22052692.

DOI:10.3390/ijms22052692
PMID:33799993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7962092/
Abstract

microRNAs (miRNAs) regulate messenger RNA (mRNA) abundance and translation during key developmental processes including muscle differentiation. Assessment of miRNA targets can provide insight into muscle biology and gene expression profiles altered by disease. mRNA and miRNA libraries were generated from C2C12 myoblasts during differentiation, and predicted miRNA targets were identified based on presence of miRNA binding sites and reciprocal expression. Seventeen miRNAs were differentially expressed at all time intervals (comparing days 0, 2, and 5) of differentiation. mRNA targets of differentially expressed miRNAs were enriched for functions related to calcium signaling and sarcomere formation. To evaluate this relationship in a disease state, we evaluated the miRNAs differentially expressed in human congenital myotonic dystrophy (CMD) myoblasts and compared with normal control. Seventy-four miRNAs were differentially expressed during healthy human myocyte maturation, of which only 12 were also up- or downregulated in CMD patient cells. The 62 miRNAs that were only differentially expressed in healthy cells were compared with differentiating C2C12 cells. Eighteen of the 62 were conserved in mouse and up- or down-regulated during mouse myoblast differentiation, and their C2C12 targets were enriched for functions related to muscle differentiation and contraction.

摘要

微小 RNA(miRNA)在包括肌肉分化在内的关键发育过程中调节信使 RNA(mRNA)的丰度和翻译。评估 miRNA 靶标可以深入了解肌肉生物学和疾病改变的基因表达谱。从 C2C12 成肌细胞在分化过程中生成 mRNA 和 miRNA 文库,并根据 miRNA 结合位点和相互表达的存在来鉴定预测的 miRNA 靶标。在分化的所有时间间隔(比较第 0、2 和 5 天),有 17 个 miRNA 差异表达。差异表达 miRNA 的 mRNA 靶标富集了与钙信号和肌节形成相关的功能。为了在疾病状态下评估这种关系,我们评估了人类先天性肌强直性营养不良(CMD)成肌细胞中差异表达的 miRNAs,并与正常对照进行了比较。在健康人类肌细胞成熟过程中表达了 74 个 miRNA,其中只有 12 个在 CMD 患者细胞中也上调或下调。仅在健康细胞中差异表达的 62 个 miRNA 与分化的 C2C12 细胞进行了比较。在这 62 个中,有 18 个在小鼠中保守,并在小鼠成肌细胞分化过程中上调或下调,其 C2C12 靶标富集了与肌肉分化和收缩相关的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c17/7962092/e96436dd35ce/ijms-22-02692-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c17/7962092/0a332ef468b2/ijms-22-02692-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c17/7962092/e96436dd35ce/ijms-22-02692-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c17/7962092/0a332ef468b2/ijms-22-02692-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c17/7962092/e96436dd35ce/ijms-22-02692-g003.jpg

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