Gli3 utilizes Hand2 to synergistically regulate tissue-specific transcriptional networks
Kelsey H Elliott,
Xiaoting Chen,
Joseph Salomone,
Praneet Chaturvedi,
Preston A Schultz,
Sai K Balchand,
Jeffrey D Servetas,
Aimée Zuniga,
Rolf Zeller,
Brian Gebelein,
Matthew T Weirauch,
Kevin A Peterson,
Samantha A Brugmann
Affiliations
Kelsey H Elliott
Division of Developmental Biology, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States; Division of Plastic Surgery, Department of Surgery, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States; Graduate Program in Molecular and Developmental Biology, Cincinnati Children's Hospital Research Foundation, Cincinnati, United States
Xiaoting Chen
Center for Autoimmune Genomics and Etiology, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States
Joseph Salomone
Division of Developmental Biology, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States; Graduate Program in Molecular and Developmental Biology, Cincinnati Children's Hospital Research Foundation, Cincinnati, United States; Medical-Scientist Training Program, University of Cincinnati College of Medicine, Cincinnati, United States
Praneet Chaturvedi
Division of Developmental Biology, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States
Preston A Schultz
Division of Developmental Biology, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States; Division of Plastic Surgery, Department of Surgery, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States
Sai K Balchand
Division of Developmental Biology, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States; Division of Plastic Surgery, Department of Surgery, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States
Jeffrey D Servetas
Jackson Laboratory, Bar Harbor, United States
Aimée Zuniga
Developmental Genetics, Department of Biomedicine, University of Basel, Basel, Switzerland
Rolf Zeller
Developmental Genetics, Department of Biomedicine, University of Basel, Basel, Switzerland
Division of Developmental Biology, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States
Matthew T Weirauch
Division of Developmental Biology, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States; Center for Autoimmune Genomics and Etiology, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States
Division of Developmental Biology, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States; Division of Plastic Surgery, Department of Surgery, Cincinnati Children’s Hospital Medical Center, Cincinnati, United States; Shriners Children’s Hospital, Cincinnati, United States
Despite a common understanding that Gli TFs are utilized to convey a Hh morphogen gradient, genetic analyses suggest craniofacial development does not completely fit this paradigm. Using the mouse model (Mus musculus), we demonstrated that rather than being driven by a Hh threshold, robust Gli3 transcriptional activity during skeletal and glossal development required interaction with the basic helix-loop-helix TF Hand2. Not only did genetic and expression data support a co-factorial relationship, but genomic analysis revealed that Gli3 and Hand2 were enriched at regulatory elements for genes essential for mandibular patterning and development. Interestingly, motif analysis at sites co-occupied by Gli3 and Hand2 uncovered mandibular-specific, low-affinity, ‘divergent’ Gli-binding motifs (dGBMs). Functional validation revealed these dGBMs conveyed synergistic activation of Gli targets essential for mandibular patterning and development. In summary, this work elucidates a novel, sequence-dependent mechanism for Gli transcriptional activity within the craniofacial complex that is independent of a graded Hh signal.