In the developing lung, different generations of conducting airways arise through reiterated branching ofepithelial tubules to form the bronchial tree. This process is accompanied by rapid changes in geneexpression and dynamic establishment of proximal-distal epithelium fate of the newly formed bud. It is alsointriguing how changes in gene expression are so quickly accomplished to precede or parallel with themorphological and cell fate changes occurring in developing buds. Genetic data in multiple organismsindicate that miRNA-mediated gene regulation plays an important role in establishing local and dynamicgene activities that are critical for cell fate determination and morphogenesis. Conditional deletion of Dicer,the RNase for maturation of miRNAs, in distal lung epithelial cells disrupts lung morphogenesis and theexpression patterns of several important genes, including FgflO, strongly suggest the critical role of miRNAin developing lung buds. The objective of this project is to study the mechanisms of miRNA pathway thatcontrol dynamic gene expression during establishment of proximal-distal cell fate in mouse embryonic lung.Our central hypothesis is that down-regulation of gene expressions mediated by miRNAs promote thedifferentiation of distal epithelial progenitor cells to form the nascent proximal structure in bifurcated budding.We have strong preliminary data to support this hypothesis, and three Aims have been designed to test thishypothesis.
In Aim one, we propose to study the broad function of miRNA pathway in proximal-distalpatterning of the lung by generating mutant mice in which Drosha or Agonaute2 is specifically mutated inlung epithelial cells. In the Aim 2, we will test the regulatory relationship and functions of several miRNAs inregulating their predicted targets both in cell line and in vivo by generating transgenic mice.
In Aim 3, weproposed to analyze global transcription expression profiles of miRNAs and mRNAs in the distal progenitorcells and in the newly formed proximal epithelial cells, and to identify key miRNAs and their targets in theproximal-distal cell differentiation. Very little is known about how the dynamic gene regulation is achievedand the role of miRNA pathway in this process. These proposed studies will significa by miRNA, and howthe proximal-distal pattern is properly established in developing lung.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
2P01HL047049-16A1
Application #
7391422
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
2007-12-01
Project End
2012-11-30
Budget Start
2007-12-01
Budget End
2009-01-31
Support Year
16
Fiscal Year
2008
Total Cost
$436,650
Indirect Cost
Name
Boston University
Department
Type
DUNS #
604483045
City
Boston
State
MA
Country
United States
Zip Code
02118
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Jiang, Zhihua; Cushing, Leah; Ai, Xingbin et al. (2014) miR-326 is downstream of Sonic hedgehog signaling and regulates the expression of Gli2 and smoothened. Am J Respir Cell Mol Biol 51:273-83
Guha, Arjun; Vasconcelos, Michelle; Zhao, Rui et al. (2014) Analysis of Notch signaling-dependent gene expression in developing airways reveals diversity of Clara cells. PLoS One 9:e88848
Jean, Jyh-Chang; George, Elizabeth; Kaestner, Klaus H et al. (2013) Transcription factor Klf4, induced in the lung by oxygen at birth, regulates perinatal fibroblast and myofibroblast differentiation. PLoS One 8:e54806
Tagne, Jean-Bosco; Gupta, Sumeet; Gower, Adam C et al. (2012) Genome-wide analyses of Nkx2-1 binding to transcriptional target genes uncover novel regulatory patterns conserved in lung development and tumors. PLoS One 7:e29907
Sommer, Cesar A; Christodoulou, Constantina; Gianotti-Sommer, Andreia et al. (2012) Residual expression of reprogramming factors affects the transcriptional program and epigenetic signatures of induced pluripotent stem cells. PLoS One 7:e51711

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