Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

The histone methyltransferase Setd7 promotes pancreatic progenitor identity

[img]
Preview
PDF (Original Article) - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
6MB
[img]
Preview
PDF (Supplementary Information) - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
923kB

Item Type:Article
Title:The histone methyltransferase Setd7 promotes pancreatic progenitor identity
Creators Name:Kofent, J. and Zhang, J. and Spagnoli, F.M.
Abstract:Cell fate specification depends on transcriptional activation driven by lineage-specific transcription factors as well as changes in chromatin organization. To date, the interplay between transcription factors and chromatin modifiers during development is not well understood. We focus here on the initiation of the pancreatic program from multipotent endodermal progenitors. Transcription factors that play key roles in regulating pancreatic progenitor state have been identified, but the chromatin regulators that help establishing and maintaining pancreatic fate are less well known. Using a comparative approach, we identify a critical role for the histone methyltransferase Setd7 in establishing pancreatic cell identity. We show that Setd7 is expressed in the prospective pancreatic endoderm of Xenopus and mouse embryos prior to Pdx1 induction. Importantly, we demonstrate that setd7 is sufficient and required for pancreatic cell fate specification in Xenopus Functional and biochemical approaches in Xenopus and mouse endoderm support that Setd7 modulates methylation marks at pancreatic regulatory regions, possibly through interaction with the transcription factor Foxa2. Together, these results demonstrate that Setd7 acts as a central component of the transcription complex initiating the pancreatic program.
Keywords:Fate Specification, Pancreas, Setd7, ESC, Animals, Mice, Xenopus
Source:Development
ISSN:0950-1991
Publisher:Company of Biologists
Volume:143
Number:19
Page Range:3573-3581
Date:1 October 2016
Official Publication:https://doi.org/10.1242/dev.136226
PubMed:View item in PubMed

Repository Staff Only: item control page

Downloads

Downloads per month over past year

Open Access
MDC Library