• About
    • Login
    View Item 
    •   Institutional Repository Home
    • Electronic Theses and Dissertations
    • Electronic Theses and Dissertations
    • View Item
    •   Institutional Repository Home
    • Electronic Theses and Dissertations
    • Electronic Theses and Dissertations
    • View Item
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Browse

    All of Institutional RepositoryCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsDepartmentThis CollectionBy Issue DateAuthorsTitlesSubjectsDepartment

    My Account

    LoginRegister

    Shh signaling in limb development

    Liu, Jiang
    : https://etd.library.vanderbilt.edu/etd-02182013-130817
    http://hdl.handle.net/1803/10583
    : 2013-02-19

    Abstract

    Sonic hedgehog (Shh), a secreted signaling molecule, is generated from the posterior limb margin and essential in regulating anterior-posterior (A-P) patterning as well as growth and differentiation of limb mesenchyme. During limb patterning, Shh acts not only upon immediate neighboring cells to induce juxtacrine signaling but also over a long distance to induce paracrine signaling. However, major gaps remain in our understanding of the molecular mechanisms by which the Shh activity gradient regulates defined patterns in the limb. Addressing this question requires a better understanding of the downstream effectors and their functions in the responsive tissue, as well as the roles of paracrine activity. As part of my thesis work, a microarray analysis is performed to identify posterior-enriched genes. Among the list, Hyaluronic Acid Synthase 2 (Has2) gene is identified as a bona fide target of Shh signaling. Two Gli-binding-sites are identified near Has2 promoter, both of which are critical for Gli transcriptional regulation during early mouse limb development. Further conditional knockout experiment in mouse embryos reveals that Has2 is critical for chondrogenesis and the positioning of the joint progenitor cells in the interzone by stabilizing chondroitin sulfate proteoglycans (CSPG) aggregate complex, providing a novel link between Shh signaling and extracellular matrix integrity during development. In addition, by generating genetic mutant of Disp1, a transmembrane protein required for Shh paracrine signaling, we observe digit loss of anterior elements, indicating that the Disp1-mediated paracrine Shh signaling is essential for digit patterning.
    Show full item record

    Files in this item

    Icon
    Name:
    ThesisJiangLiu.pdf
    Size:
    10.10Mb
    Format:
    PDF
    View/Open

    This item appears in the following collection(s):

    • Electronic Theses and Dissertations

    Connect with Vanderbilt Libraries

    Your Vanderbilt

    • Alumni
    • Current Students
    • Faculty & Staff
    • International Students
    • Media
    • Parents & Family
    • Prospective Students
    • Researchers
    • Sports Fans
    • Visitors & Neighbors

    Support the Jean and Alexander Heard Libraries

    Support the Library...Give Now

    Gifts to the Libraries support the learning and research needs of the entire Vanderbilt community. Learn more about giving to the Libraries.

    Become a Friend of the Libraries

    Quick Links

    • Hours
    • About
    • Employment
    • Staff Directory
    • Accessibility Services
    • Contact
    • Vanderbilt Home
    • Privacy Policy