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腱调蛋白是一种转录激活因子,可调节成熟腱细胞和韧带细胞标志物腱调蛋白的表达。

Scleraxis is a transcriptional activator that regulates the expression of Tenomodulin, a marker of mature tenocytes and ligamentocytes.

机构信息

Department of Molecular Biology and Biochemistry, Division of Dental Sciences, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, 734-8553, Japan.

Laboratory of Cellular Differentiation, Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, 606-8507, Japan.

出版信息

Sci Rep. 2018 Feb 16;8(1):3155. doi: 10.1038/s41598-018-21194-3.

Abstract

Tenomodulin (Tnmd) is a type II transmembrane glycoprotein predominantly expressed in tendons and ligaments. We found that scleraxis (Scx), a member of the Twist-family of basic helix-loop-helix transcription factors, is a transcriptional activator of Tnmd expression in tenocytes. During embryonic development, Scx expression preceded that of Tnmd. Tnmd expression was nearly absent in tendons and ligaments of Scx-deficient mice generated by transcription activator-like effector nucleases-mediated gene disruption. Tnmd mRNA levels were dramatically decreased during serial passages of rat tenocytes. Scx silencing by small interfering RNA significantly suppressed endogenous Tnmd mRNA levels in tenocytes. Mouse Tnmd contains five E-box sites in the ~1-kb 5'-flanking region. A 174-base pair genomic fragment containing a TATA box drives transcription in tenocytes. Enhancer activity was increased in the upstream region (-1030 to -295) of Tnmd in tenocytes, but not in NIH3T3 and C3H10T1/2 cells. Preferential binding of both Scx and Twist1 as a heterodimer with E12 or E47 to CAGATG or CATCTG and transactivation of the 5'-flanking region were confirmed by electrophoresis mobility shift and dual luciferase assays, respectively. Scx directly transactivates Tnmd via these E-boxes to positively regulate tenocyte differentiation and maturation.

摘要

腱调蛋白(Tnmd)是一种 II 型跨膜糖蛋白,主要在肌腱和韧带中表达。我们发现,粘连蛋白(Scx)是 Twist 家族碱性螺旋-环-螺旋转录因子的成员,是肌腱细胞中 Tnmd 表达的转录激活子。在胚胎发育过程中,Scx 的表达先于 Tnmd。通过转录激活子样效应物核酶介导的基因敲除生成的 Scx 缺陷型小鼠的肌腱和韧带中几乎没有 Tnmd 表达。大鼠肌腱细胞连续传代时,Tnmd mRNA 水平显著降低。小干扰 RNA 沉默 Scx 可显著抑制肌腱细胞中内源性 Tnmd mRNA 水平。小鼠 Tnmd 在 ~1kb 的 5'侧翼区含有五个 E-box 位点。一个包含 TATA 盒的 174 碱基对基因组片段可在肌腱细胞中驱动转录。在肌腱细胞中,Tnmd 上游区域(-1030 至-295)的增强子活性增加,但在 NIH3T3 和 C3H10T1/2 细胞中没有。电泳迁移率变动分析和双荧光素酶检测分别证实了 Scx 和 Twist1 作为 E12 或 E47 的异二聚体与 CAGATG 或 CATCTG 的优先结合以及 5'侧翼区的转录激活。Scx 通过这些 E-box 直接激活 Tnmd,以正向调节肌腱细胞分化和成熟。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c19a/5816641/4df6a950e6e3/41598_2018_21194_Fig1_HTML.jpg

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