R03: Genetic Control of Post-Embryonic Developmental Progression in Zebrafish Project Summary/Abstract We still very little about the mechanisms of morphogenesis and differentiation during post- embryonic developmental stages in vertebrates. Nonetheless, understanding the factors regulating these later developmental periods is essential to understanding how adult traits form, and will lend insight into morphological defects and disorders that arise during human post- embryonic fetal and neonatal periods. This research utilizes the zebrafish, which undergoes extensive post-embryonic development involving changes in a variety of organ systems, changes similar or identical to processes that occur in prenatal humans. This proposal takes a two-pronged strategy towards understanding the genetic controls of the larval-to-adult transition in zebrafish.
The first aim adopts a targeted approach, concentrating on two mutants that undergo complete somatic arrest during larval development, arresting after two and three weeks of development, respectively. These phenotypes suggest an impairment of genes absolutely required for post-embryonic developmental progression;mapping and cloning the mutations and characterizing the pathways will reveal some of the genes required for developmental processes occurring after embryogenesis. Since so little is known about the molecular changes involved in post-embryonic developmental progression, the second aim of this proposal represents an exploratory strategy that will extensively characterize transcriptional changes that occur during key developmental transitions. Transcriptomes will be produced for the skin, which undergoes well-characterized tissue-level transformations at post-embryonic stages, and the brain, which undergoes extensive neuronal maturation and neurogenesis during larval-to-adult transformation. Further, many of the global endocrine cascades that regulate growth and development originate in the brain. Transcript abundance will be quantified at different stages in each organ for both known and unknown mRNAs, including any splice variants. Since microRNAs are so crucial in regulating stage transitions in invertebrates, temporal expression of small, non-coding RNAs will also be fully characterized. These post-embryonic developmental transcriptomes will serve as resources to the larger research community and will allow detection of molecules and pathways that may mediate post-embryonic transitions. Dynamic expression profiles will further allow full characterization of the molecular phenotypes of the developmental arrest mutants. Overall, these efforts will generate resources for future studies of post- embryonic transitions and will identify novel factors that regulate and are required for normal progression through post-embryonic developmental stages.

Public Health Relevance

R03: Genetic Control of Post-Embryonic Developmental Progression in Zebrafish Project Narrative The larval-to-adult transformation in zebrafish includes many processes analogous to those occurring in human embryonic, fetal and neonatal development;despite clear biomedical relevance, we know very little about the mechanisms controlling the processes occurring during this transitional period. The proposed research will map and clone two mutations causing larval developmental arrest, revealing potentially novel genetic requirements for post-embryonic stage progression. Further, genes and RNAs active at different stages of the larval-to-adult transformation will be extensively characterized, and will serve as the first step towards identifying factors regulating transitions between post-embryonic stages.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Small Research Grants (R03)
Project #
1R03HD074787-01
Application #
8427198
Study Section
Pediatrics Subcommittee (CHHD)
Program Officer
Winer, Karen
Project Start
2012-12-20
Project End
2014-12-31
Budget Start
2012-12-20
Budget End
2013-12-31
Support Year
1
Fiscal Year
2013
Total Cost
$77,250
Indirect Cost
$27,250
Name
University of Washington
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
McMenamin, Sarah K; Bain, Emily J; McCann, Anna E et al. (2014) Thyroid hormone-dependent adult pigment cell lineage and pattern in zebrafish. Science 345:1358-61