Suppr超能文献

鉴定节段性表达所需的Epha4增强子以及Mesp2对其的调控。

Identification of Epha4 enhancer required for segmental expression and the regulation by Mesp2.

作者信息

Nakajima Yoshiro, Morimoto Mitsuru, Takahashi Yuki, Koseki Haruhiko, Saga Yumiko

机构信息

Division of Mammalian Development, National Institute of Genetics, Yata 1111, Mishima 411-8540, Japan.

出版信息

Development. 2006 Jul;133(13):2517-25. doi: 10.1242/dev.02422. Epub 2006 May 25.

Abstract

Somites provide the basic body plan for metameric axial structures in vertebrates, and establish the segmental features through the sequential gene expression in the presomitic mesoderm (PSM). A crucial protein for segment border formation is the bHLH transcription factor Mesp2, the expression of which is restricted to the anterior PSM. A gene candidate that is activated by Mesp2 is Epha4, as its expression pattern resembles Mesp2 and is absent in Mesp2-null embryos. We have analyzed the enhancer region of Epha4, which is responsible for its expression in the anterior PSM, and identified an E-box containing region. Subsequent transgenic and transient luciferase analyses successfully determined that the presence of repeated E-box sequences is a minimum essential requirement for the expression in the anterior PSM. We also show that Mesp2 directly binds to the enhancer sequence of Epha4. Furthermore, the forced expression of Mesp2 in somitic cells results in the activation of Epha4 and repression of the caudal gene Uncx4.1, which may trigger the events leading to the formation of abnormal somites and rostralized vertebra. In addition, ectopic Mesp2 expression induces abnormally epithelialized structures, which support to the idea that Mesp2 induces the formation of segmental borders by activating genes that play roles in cellular epithelialization.

摘要

体节为脊椎动物的分节轴向结构提供基本的身体蓝图,并通过体节中胚层(PSM)中的顺序基因表达来建立节段特征。对于节段边界形成至关重要的一种蛋白质是bHLH转录因子Mesp2,其表达仅限于PSM的前部。一个由Mesp2激活的候选基因是Epha4,因为它的表达模式与Mesp2相似,并且在Mesp2基因敲除的胚胎中不存在。我们分析了Epha4的增强子区域,该区域负责其在PSM前部的表达,并鉴定出一个含有E-box的区域。随后的转基因和瞬时荧光素酶分析成功确定,重复的E-box序列的存在是在PSM前部表达的最低必要条件。我们还表明,Mesp2直接与Epha4的增强子序列结合。此外,Mesp2在体节细胞中的强制表达导致Epha4的激活和尾部基因Uncx4.1的抑制,这可能引发导致异常体节和头化椎骨形成的事件。此外,异位Mesp2表达诱导异常上皮化结构,这支持了Mesp2通过激活在细胞上皮化中起作用的基因来诱导节段边界形成的观点。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验