Cooperative Transcriptional Regulation of the Essential Pancreatic Islet Gene NeuroD1 (Beta2) by Nkx2.2 and Neurogenin 3*

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American Society for Biochemistry and Molecular Biology

RESUMO

Nkx2.2 and NeuroD1 are two critical regulators of pancreatic β cell development. Nkx2.2 is a homeodomain transcription factor that is essential for islet cell type specification and mature β cell function. NeuroD1 is a basic helix-loop-helix transcription factor that is critical for islet β cell maturation and maintenance. Although both proteins influence β cell development directly downstream of the endocrine progenitor factor, neurogenin3 (Ngn3), a connection between the two proteins in the regulation of β cell fate and function has yet to be established. In this study, we demonstrate that Nkx2.2 transcriptional activity is required to facilitate the activation of NeuroD1 by Ngn3. Furthermore, Nkx2.2 is necessary to maintain high levels of NeuroD1 expression in developing mouse and zebrafish islets and in mature β cells. Interestingly, Nkx2.2 regulates NeuroD1 through two independent promoter elements, one that is bound and activated directly by Nkx2.2 and one that appears to be regulated by Nkx2.2 through an indirect mechanism. Together, these findings suggest that Nkx2.2 coordinately activates NeuroD1 with Ngn3 within the endocrine progenitor cell and also plays a role in the maintenance of NeuroD1 expression to regulate β cell function in the mature islet. Collectively, these findings further define the conserved regulatory networks involved in islet β cell formation and function.

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