Grant: Discovery Grants Program - Individual
Dalhousie University
$65,000.00
Development and evolution of vertebrate skeletal tissues
FY 2011-12
Summary
I study how the skeleton of embryos of fish and frogs form. I should say skeletons; all vertebrates have had two skeletons for almost 500 million years; an exo- and an endoskeleton. Most of the human or dinosaur bones you see in a museum are the inside (endo) skeleton, which is based on cartilage, most of which is replaced by bone. Your arm skeleton is part of the endoskeleton. The second skeleton was originally on the outside and so is an exoskeleton. Originally it consisted of bone and dentine (the tissue found in teeth), either as small isolated plates or as plates fused into an external armor. During evolution, some plates sank below the surface as teeth and to form the clavicle (collar bone) and parts of the skull. These two skeletons have distinct developmental and evolutionary histories. Currently, we are investigating skeletal development in frogs and fish. Frogs are fascinating because the tadpole skeleton is based in cartilage but the adult skeleton is based on bone. We want to know how much of the tadpole skull skeleton is carried over to adult frogs. If not carried over then do adult skeletal elements form from a line of cells distinct from those that form the tadpole cartilaginous skeleton? We tag genes that are specific for cartilage or bone onto green fluorescent protein (GFP) and inject the construct into frog eggs. The resulting eggs have green cartilages or bones. If the construct is incorporated into cells that make eggs and sperm, then the skeleton of the next generation will also glow green. By using different gene constructs we can track cells making different skeletal tissues during the frog's lifetime. We know the skeletal tissues in frogs - they are cartilage and bone. The situation is much less clear-cut in fish, in which transitions between cartilage and bone occur. Our fish project will identify the types of skeletal tissues and transitions between tissues. Once known, we use gene probes to reveal the cell populations that make these tissues. Because as much as 30% of fish in hatcheries may never make it to market because of skeletal deformities that make the fish unattractive to potential customers, this approach has potential significance for the aquaculture industry and the economy.
Program
Discovery Grants Program - Individual
Recipient
Location
Nova Scotia, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
5056-2011
Name nom
Hall, Brian
Department département
Biology
Organization id
79
Institution établissement
Dalhousie University
Province en
Nova Scotia
Province fr
Nouvelle-Écosse
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2011
Competition year année de concours
2011
Award amount
65000
Program id
RGPIN
Program nane en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1502
Committee name en
Biological Systems and Functions
Committee name fr
Systèmes et fonctions biologiques
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
5509
Research subject group en
Animal biology
Research subject group fr
Biologie animale
Research subject en
Animal morphology
Research subject fr
Morphologie animale
Partie
1
Nb partie
5
Application title
Development and evolution of vertebrate skeletal tissues
Keyword
NSERC
Application summary
I study how the skeleton of embryos of fish and frogs form. I should say skeletons; all vertebrates have had two skeletons for almost 500 million years; an exo- and an endoskeleton. Most of the human or dinosaur bones you see in a museum are the inside (endo) skeleton, which is based on cartilage, most of which is replaced by bone. Your arm skeleton is part of the endoskeleton. The second skeleton was originally on the outside and so is an exoskeleton. Originally it consisted of bone and dentine (the tissue found in teeth), either as small isolated plates or as plates fused into an external armor. During evolution, some plates sank below the surface as teeth and to form the clavicle (collar bone) and parts of the skull. These two skeletons have distinct developmental and evolutionary histories. Currently, we are investigating skeletal development in frogs and fish. Frogs are fascinating because the tadpole skeleton is based in cartilage but the adult skeleton is based on bone. We want to know how much of the tadpole skull skeleton is carried over to adult frogs. If not carried over then do adult skeletal elements form from a line of cells distinct from those that form the tadpole cartilaginous skeleton? We tag genes that are specific for cartilage or bone onto green fluorescent protein (GFP) and inject the construct into frog eggs. The resulting eggs have green cartilages or bones. If the construct is incorporated into cells that make eggs and sperm, then the skeleton of the next generation will also glow green. By using different gene constructs we can track cells making different skeletal tissues during the frog's lifetime. We know the skeletal tissues in frogs - they are cartilage and bone. The situation is much less clear-cut in fish, in which transitions between cartilage and bone occur. Our fish project will identify the types of skeletal tissues and transitions between tissues. Once known, we use gene probes to reveal the cell populations that make these tissues. Because as much as 30% of fish in hatcheries may never make it to market because of skeletal deformities that make the fish unattractive to potential customers, this approach has potential significance for the aquaculture industry and the economy.