Grant: Discovery Grants Program - Individual
University of Regina
$27,328.00
Thyroid regulation of fish development: physiological, cellular and molecular responses with evolutionary considerations
FY 2007-08
Summary
This research program combines studies in thyroid hormone physiology, molecular biology and gene regulation to decipher the internal signals that regulate the dramatic developmental event of metamorphosis in lampreys. Lamprey metamorphosis is analogous to the metamorphosis that transforms a fish-like tadpole into a frog. Lampreys are one of the most ancient living vertebrates (animals with a spinal column, including humans) and are a good model to study the evolution of developmental regulation and vertebrate ancestry. Interestingly, the start of lamprey metamorphosis coincides with a dramatic drop in thyroid hormone levels. This drop is opposite to the surge in thyroid hormone levels seen at the beginning of major developmental events in other vertebrates. The aims of this research program are to determine if this paradox of lamprey metamorphosis represents a fundamental difference in how thyroid hormones control development in lamprey (i.e. gene regulation) or more simply a difference in the physiological and cellular regulation of active hormone. Specifically this program will decipher the function and role in development of: a) systems in lamprey blood that transport thyroid hormones b) the enzymes that activate and inactivate the hormones in the cell and c) the receptors to which hormones bind to modulate gene activity. Lastly, we will also identify the lamrpey genes that are controlled by thyroid hormones and potentially drive metamorphosis. My research program will advance our understanding of the regulation of thyroid hormones and their role in the development of ancient vertebrates. Thyroid hormones are involved in many important biological processes in vertebrates including: development, growth, fat metabolism, temperature regulation, immune defense and reproduction. The unique nature of the lamprey thyroid system and its role in lamprey development may offer new insights into vertebrate thyroid physiology and dysfunction. Lastly, a better understanding of the factors that control lamprey development will provide novel opportunities to develop environmentally benign measures to control sea lamprey populations in the Great Lakes and reduce our reliance on current chemical treatments.
Program
Discovery Grants Program - Individual
Recipient
Location
Saskatchewan, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
261948-2007
Name nom
Manzon, Richard
Department département
Biology
Organization id
17
Institution établissement
University of Regina
Province en
Saskatchewan
Province fr
Saskatchewan
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2007
Competition year année de concours
2007
Award amount
27328
Program id
RGPIN
Program name 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
1011
Committee name en
Integrative Animal Biology
Committee name fr
Biologie Animale Intégrative
Area of application code
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
5503
Research subject group en
Animal biology
Research subject group fr
Biologie animale
Research subject en
Endocrinology
Research subject fr
Endocrinologie
Partie
1
Nb partie
2
Application title
Thyroid regulation of fish development: physiological, cellular and molecular responses with evolutionary considerations
Keyword
NA
Application summary
This research program combines studies in thyroid hormone physiology, molecular biology and gene regulation to decipher the internal signals that regulate the dramatic developmental event of metamorphosis in lampreys. Lamprey metamorphosis is analogous to the metamorphosis that transforms a fish-like tadpole into a frog. Lampreys are one of the most ancient living vertebrates (animals with a spinal column, including humans) and are a good model to study the evolution of developmental regulation and vertebrate ancestry. Interestingly, the start of lamprey metamorphosis coincides with a dramatic drop in thyroid hormone levels. This drop is opposite to the surge in thyroid hormone levels seen at the beginning of major developmental events in other vertebrates. The aims of this research program are to determine if this paradox of lamprey metamorphosis represents a fundamental difference in how thyroid hormones control development in lamprey (i.e. gene regulation) or more simply a difference in the physiological and cellular regulation of active hormone. Specifically this program will decipher the function and role in development of: a) systems in lamprey blood that transport thyroid hormones b) the enzymes that activate and inactivate the hormones in the cell and c) the receptors to which hormones bind to modulate gene activity. Lastly, we will also identify the lamrpey genes that are controlled by thyroid hormones and potentially drive metamorphosis. My research program will advance our understanding of the regulation of thyroid hormones and their role in the development of ancient vertebrates. Thyroid hormones are involved in many important biological processes in vertebrates including: development, growth, fat metabolism, temperature regulation, immune defense and reproduction. The unique nature of the lamprey thyroid system and its role in lamprey development may offer new insights into vertebrate thyroid physiology and dysfunction. Lastly, a better understanding of the factors that control lamprey development will provide novel opportunities to develop environmentally benign measures to control sea lamprey populations in the Great Lakes and reduce our reliance on current chemical treatments.