The heterochronic pathway in Caenorhabditis elegans controls the timing of developmental events. One member of this regulatory pathway is lin-4. The product of lin-4 is a phylogenetically conserved founding member a large class of small noncoding RNAs known as microRNAs (miRNAs). The expression of lin-4 is activated at a specific time during the worm's post-embryonic development and acts by repressing the translation of target mRNAs by hybridizing to their 3' untranslated region. Although nematode miRNAs are some of the best-characterized miRNAs to date, the elements and factors that govern the specificity of their temporal expression are unknown. Preliminary data from the Ambros laboratory suggest that the expression of lin-4 may be transcriptionally regulated. In addition, there is evidence from the Ambros lab that at least two previously uncharacterized proteins may be involved in the regulation of lin-4 in the worm. The objectives of this proposal are to characterize the role of these candidate proteins in modulating the expression of lin-4, and to identify and characterize cis-acting and other trans-acting regulatory elements that participate in temporal expression of lin-4 in C. elegans. Understanding how the expression of lin-4 occurs in the nematode can provide valuable insights on how animal development, including that of mammals, is regulated.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM070118-02
Application #
6845127
Study Section
Special Emphasis Panel (ZRG1-F05 (20))
Program Officer
Tompkins, Laurie
Project Start
2004-02-01
Project End
2006-01-31
Budget Start
2005-02-01
Budget End
2006-01-31
Support Year
2
Fiscal Year
2005
Total Cost
$49,928
Indirect Cost
Name
Dartmouth College
Department
Genetics
Type
Schools of Medicine
DUNS #
041027822
City
Hanover
State
NH
Country
United States
Zip Code
03755
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Martinez, Natalia J; Ow, Maria C; Barrasa, M Inmaculada et al. (2008) A C. elegans genome-scale microRNA network contains composite feedback motifs with high flux capacity. Genes Dev 22:2535-49
Ow, Maria C; Martinez, Natalia J; Olsen, Philip H et al. (2008) The FLYWCH transcription factors FLH-1, FLH-2, and FLH-3 repress embryonic expression of microRNA genes in C. elegans. Genes Dev 22:2520-34