Computational and Functional Analysis of Gene Networks
Computational and Functional Analysis of Gene Networks
批准号:
6863973
负责人:
MARC S HALFON
金额:
$13.16万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-07-01 至 2007-06-30
关键词:
Drosophilidae animal genetic material tag binding sites biological signal transduction computer data analysis computer program /software computer system design /evaluation epidermal growth factor fibroblast growth factor flow cytometry functional /structural genomics gene expression genetic enhancer element genetic regulatory element genetic transcription growth factor receptors mathematical model microarray technology molecular cloning nucleic acid sequence polymerase chain reaction regulatory gene transcription factor
中文摘要
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英文摘要
DESCRIPTION: (provided by applicant) Metazoan development requires both
intercellular signaling and the integration of these signals within cells to
produce a transcriptional response. While many signaling pathways are well
characterized, understanding on a global scale the interplay between signal
transduction and gene transcription - genetic regulatory networks -remains a
major challenge for current genomics research. We have explored in detail part
of one such network, which specifies the fate of a subset of Drosophilamuscle
and cardiac progenitor cells by the combined action of three signaling
pathways, including the Ras pathway via input from both EGF and FGF receptors.
The transcription factors downstream of these pathways, and tissue-specific
factors induced by them, are integrated at a single transcriptional enhancer
for a progenitor identity gene, the even skippedMuscle and Heart Enhancer
(MHE). Therecent sequencing of the Drosophilagenome offers an exciting
opportunity to extend the insights garnered from our investigation of the MHE
on a genome-wide scale. Here, a computational analysis will be used to identify
cis-regulatory elements that share features of the MHE and that regulate
mesodermal gene expression in a similar spatiotemporal pattern. Invivo
techniques, including the analysis of reporter transgenes, will be used to
validate the computer predictions. The signaling component of the regulatory
networks in which these cisregulatory elements act will be investigated using
DNA microarrays. The respective contributions of the FGF and EGF-receptor
pathways to Ras-mediated mesodermal signaling, non-Ras-mediated activities of
these receptors, and the individual contributions of specific Ras
transcriptional effectors will be determined, as will the combined effects of
multiple growth factor signals. These approaches will significantly increase
our understanding of combinatorial signaling and transcriptional responses by
identifying new genes and regulatory elements, and provide insight into the
genetic regulatory networks that mediate responses to signaling in a specific
regulatory context.
The research detailed in this proposal will provide the candidate with an ideal
opportunity to apply a strong background in developmental genetics to the
emerging fields of computational and functional genomics in a rich learning and
research environment, in preparation for an independent academic research
career.
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财政年份:2008
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资助金额:$33.05万
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负责人:MARC S HALFON
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依托单位: