Project Grant R35GM154889
- The National Institute of Child Health and Human Development (NICHD), through its Child Health and Human Development Extramural Research Federal Grant Program (CFDA 93.865), awarded Wake Forest University a $390,101 Project Grant to develop new viral toolkits for investigating the molecular mechanisms driving limb regeneration in the Mexican axolotl salamander. The two-year project aims to validate viral gene delivery methods in the axolotl limb and combine these tools with transgenic and...
- This federal Project Grant award for $169,000.00, provided by the National Institute of Child Health and Human Development (NICHD) under the Child Health and Human Development Extramural Research program (CFDA 93.865), supports the development of a single-cell reference atlas of axolotl embryogenesis. The overarching goal is to elucidate the fundamental biological processes required for limb regeneration, with the aim of informing future regenerative medicine strategies for human limb injuries...
- This $687,427 Project Grant awarded by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), under the Federal Grant Program 93.865 - Child Health and Human Development Extramural Research, aims to investigate the role of macrophages in guiding digit regeneration. The project leverages a comparative mouse model of bone regeneration and scar formation to study a unique population of macrophages that associates with growing bone and expresses growth factors...
- This $294,408 Project Grant award from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) under the Child Health and Human Development Extramural Research program (CFDA 93.865) supports research at the University of Oregon to further understand how cell signaling mediates cell-cell interactions to facilitate intricate skeletal patterning during zebrafish fin regeneration. The research aims to identify the key Sonic Hedgehog (SHH) signaling target genes...
- This federal Project Grant award, valued at $351,920.00 and provided by the National Institute of General Medical Sciences (CFDA 93.859 Biomedical Research and Research Training program), supports research by the University of Southern California (USC) focused on understanding the fundamental requirements for blastema development - the formation of specialized regenerative structures - in lizard species. The research aims to identify genetic and molecular signatures associated with the loss of...
- This Project Grant award from the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), under the Child Health and Human Development Extramural Research program (CFDA 93.865), is focused on understanding how mechanical load regulates mammalian digit regeneration. The $485,782 award to Texas A&M AgriLife Research, a component of the Texas A&M University System, will fund research to determine the role of mechanical load in both endogenous and induced...
- This Project Grant award from the National Institutes of Health (NIH) Office of the Director under the Trans-NIH Research Support program (CFDA 93.310) provides $1,359,000.00 to Baylor College of Medicine to conduct research on age-associated cellular and molecular adaptations that enable whole-organism rejuvenation in the highly regenerative flatworm Schmidtea mediterranea. The research aims to (1) determine how age-associated damage manifests in asexual planaria throughout their lifecycle...
- This $156,080 Project Grant was awarded by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) under the Child Health and Human Development Extramural Research program (CFDA 93.865). The grant was awarded to Oregon Health & Science University (UEI: NPSNT86JKN51) to conduct research aimed at identifying the factors that define neural stem cells (NSCs) in the spinal cord and their role in regenerating the central nervous system (CNS) in response to...
- This Project Grant award from the National Institute of General Medical Sciences (NIGMS) Biomedical Research and Research Training program (CFDA 93.859) provides $387,500.00 to The Johns Hopkins University from January 1, 2025 to November 30, 2029 to elucidate the gene regulatory networks that control hair cell regeneration in zebrafish. The research aims to identify key transcription factors, such as SOX and SIX, that regulate the transition of support cells to a progenitor state capable of...
- This $428,600 federal Project Grant award from the National Institute of General Medical Sciences (NIGMS), under the Biomedical Research and Research Training program (CFDA 93.859), supports an investigation into how RNA-directed feedback loops coordinate wound healing and regeneration. The research project aims to understand the conserved developmental pathways and heterochronic genes that regulate cell migration, fate, and timing during normal adult wound repair and regeneration,...
HOX GENE REGULATION OF BODY SIZE AND ASEXUAL REPRODUCTION UNDERLIE REGENERATIVE ABILITIES - ABSTRACT THE ABILITY OF CERTAIN ANIMALS TO REGENERATE THEIR CELLS AND TISSUES HAS LONG BEEN A SUBJECT OF INTEREST FOR BIOLOGISTS DUE TO ITS RELEVANCE TO ANIMAL DEVELOPMENT AND REGENERATIVE MEDICINE. HOWEVER, WE STILL DON'T FULLY UNDERSTAND WHY SOME ANIMALS REGENERATE SO WELL, WHILE OTHERS CANNOT. FROM A HOLISTIC PERSPECTIVE, THE LOSS OF REGENERATIVE CAPACITY IN VERTEBRATES CORRELATES WITH THE EVOLUTION OF LARGER AND MORE COMPLEX BODY PLANS AS WELL AS THE LOSS OF ASEXUAL REPRODUCTION. HOWEVER, IT'S UNCLEAR HOW BODY SIZE OR ANATOMICAL COMPLEXITY AFFECTS REGENERATIVE PROCESSES, AND THE ROLE OF ASEXUAL REPRODUCTION IN THIS PROCESS IS UNKNOWN. THIS KNOWLEDGE GAP CENTERS ON A FUNDAMENTAL PRINCIPLE UNDERLYING THE DIFFERENTIAL REGENERATIVE PROPERTIES OF ANIMALS AND THEIR TISSUES. HOX GENES ARE CONSERVED TRANSCRIPTIONAL REGULATORS KEY TO THE EVOLUTIONARY DIVERSIFICATION OF BODY PLANS. ALTHOUGH HOX GENES HAVE BEEN EXTENSIVELY STUDIED IN ANIMALS WITH LIMITED REGENERATIVE CAPABILITIES, THEIR FUNCTIONS IN ANIMALS CAPABLE OF WHOLE-BODY REGENERATION ARE NOT WELL UNDERSTOOD. A BETTER UNDERSTANDING OF HOX GENE FUNCTIONS IN HIGHLY REGENERATIVE ORGANISMS COULD PROVIDE VALUABLE INSIGHT INTO THE BODY PLAN FEATURES THAT UNDERLIE THE RETENTION AND MODIFICATION OF REGENERATIVE ABILITIES. AS A TRAINEE, I HAVE DISCOVERED THAT HOX GENES REGULATE ASEXUAL REPRODUCTION IN PLANARIA, A FLATWORM THAT CAN REGENERATE ITS ENTIRE BODY. THIS INVERTEBRATE MODEL'S POTENT REGENERATIVE ABILITIES AND AMENABILITY TO ADVANCED MOLECULAR ANALYSIS AND LARGE-SCALE GENE INTERFERENCE SCREENS MAKE IT IDEAL FOR STUDYING THE FUNDAMENTAL MECHANISMS OF ANIMAL REGENERATION. OUR RECENT PRELIMINARY DATA REVEAL A NEW ROLE OF HOX GENES IN LIMITING THE BODY SIZE OF PLANARIANS. TAKING ADVANTAGE OF THIS FINDING, WE GENERATED ANIMALS FIVE TIMES THEIR NORMAL SIZE AND DISCOVERED THAT PLANARIAN REGENERATIVE ABILITIES CANNOT FUNCTIONALLY SCALE IN AN EXPANDED BODY PLAN. FINALLY, WE HAVE IDENTIFIED GENES WITH DUAL FUNCTIONS IN BOTH WHOLE-BODY REGENERATION AND ASEXUAL REPRODUCTION FROM A LARGE RNAI SCREEN OF TRANSCRIPTIONAL REGULATORS, WHICH LAYS THE FOUNDATION FOR UNCOVERING A SHARED GENE REGULATORY NETWORK LINKING THESE PROCESSES. THROUGH THE MECHANISTIC DISSECTION OF HOW HOX GENES SUPPORT PLANARIAN WHOLE-BODY REGENERATION, I AIM TO EXPAND OUR UNDERSTANDING OF THE FUNCTIONS OF THESE KEY DEVELOPMENTAL GENES WHILE PROVIDING IMPORTANT INSIGHT INTO THE FUNDAMENTAL PRINCIPLES DISTINGUISHING REGENERATIVE VERSUS NON-REGENERATIVE BODY PLANS. THIS WORK HAS THE POTENTIAL TO ENHANCE OUR UNDERSTANDING OF THE PERMISSIVE FACTORS UNDERLYING TISSUE REGENERATION AND TO INSPIRE AND INFORM NOVEL APPROACHES TO IMPROVING HUMAN HEALTH.
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $380.0k | 4/15/25 | ||
| Not listed | $380.0k | 7/11/24 | ||
| Not listed | $380.0k | 7/11/24 |