Sox17的阳性自动调节对于胆囊和肝外胆管的形成是必要的。

IF 3.7 2区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Development Pub Date : 2025-01-15 Epub Date: 2025-01-16 DOI:10.1242/dev.203033
Linh T Trinh, Ryan R Finnel, Anna B Osipovich, Jessica R Musselman, Leesa L Sampson, Christopher V E Wright, Mark A Magnuson
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引用次数: 0

摘要

SRY-box转录因子17 (Sox17)在原肠胚后期肝憩室尾侧内胚层区域的表达是肝-胰-胆系统形成所必需的。对Sox17转录起始位点(TSS) 2附近启动子-近端突变等位基因系列的分析表明,胆囊(GB)和肝外胆管(EHBD)的发育对Sox17的表达水平非常敏感。TSS2启动子中sox17结合的顺式调控元件的缺失通过减少新生胆管的生长来损害GB&EHBD的发展。这些发现揭示了Sox17依赖的自调节回路的存在,该回路驱动Sox17的表达高于GB&EHBD发生所需的临界阈值浓度,并且Sox17基因表达的轻微损伤足以损害新生GB&EHBD系统中Sox17调节基因的表达,从而损害或阻止发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Positive autoregulation of Sox17 is necessary for gallbladder and extrahepatic bile duct formation.

Expression of SRY-box transcription factor 17 (Sox17) in the endodermal region caudal to the hepatic diverticulum during late gastrulation is necessary for hepato-pancreato-biliary system formation. Analysis of an allelic series of promoter-proximal mutations near the transcription start site (TSS) 2 of Sox17 in mouse has revealed that gallbladder (GB) and extrahepatic bile duct (EHBD) development is exquisitely sensitive to Sox17 expression levels. Deletion of a SOX17-binding cis-regulatory element in the TSS2 promoter impairs GB and EHBD development by reducing outgrowth of the nascent biliary bud. These findings reveal the existence of a SOX17-dependent autoregulatory loop that drives Sox17 expression above a critical threshold concentration necessary for GB and EHBD development to occur, and that minor impairments in Sox17 gene expression are sufficient to impair the expression of SOX17-regulated genes in the nascent GB and EHBD system, impairing or preventing development.

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来源期刊
Development
Development 生物-发育生物学
CiteScore
6.70
自引率
4.30%
发文量
433
审稿时长
3 months
期刊介绍: Development’s scope covers all aspects of plant and animal development, including stem cell biology and regeneration. The single most important criterion for acceptance in Development is scientific excellence. Research papers (articles and reports) should therefore pose and test a significant hypothesis or address a significant question, and should provide novel perspectives that advance our understanding of development. We also encourage submission of papers that use computational methods or mathematical models to obtain significant new insights into developmental biology topics. Manuscripts that are descriptive in nature will be considered only when they lay important groundwork for a field and/or provide novel resources for understanding developmental processes of broad interest to the community. Development includes a Techniques and Resources section for the publication of new methods, datasets, and other types of resources. Papers describing new techniques should include a proof-of-principle demonstration that the technique is valuable to the developmental biology community; they need not include in-depth follow-up analysis. The technique must be described in sufficient detail to be easily replicated by other investigators. Development will also consider protocol-type papers of exceptional interest to the community. We welcome submission of Resource papers, for example those reporting new databases, systems-level datasets, or genetic resources of major value to the developmental biology community. For all papers, the data or resource described must be made available to the community with minimal restrictions upon publication. To aid navigability, Development has dedicated sections of the journal to stem cells & regeneration and to human development. The criteria for acceptance into these sections is identical to those outlined above. Authors and editors are encouraged to nominate appropriate manuscripts for inclusion in one of these sections.
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