ANALYSIS OF EARLY WING VEIN DEVELOPMENT IN DROSPHILIA
ANALYSIS OF EARLY WING VEIN DEVELOPMENT IN DROSPHILIA
批准号:
6343106
负责人:
ETHAN BIER
金额:
$21.57万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-01-01 至 2003-12-31
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (adapted from investigator's abstract): The long term goal of this
proposal is to understand how wing vein development is initiated in Drosophila
wing imaginal discs. Five major veins run the length of the Drosophila wing. We
have proposed that wing vein development is initiated at boundaries between
distinct domains of cells situated along the anterior-posterior (A/P) axis of
the wing imaginal disc in third instar larvae. In our convincing case for this
hypothesis, we have provided a variety of evidence indicating that development
of the second longitudinal vein (L2) is induced just anterior to a broad
central domain of cells expressing a zinc finger transcription factor known as
spalt- major (salm). We have proposed that salm expressing cells send a signal
to adjacent anterior cells to activate expression of hormonereceptor family
transcription factors encoded by genes at the knirpslknirps-related (kni/knrl)
locus. The kni and knrl genes then function to organize gene expression in and
around the L2 vein primordium. In this proposal we seek to understand the
mechanism by which salm expressing cells activate kni and knrl expression in
neighboring anterior cells by analyzing an enhancer element of the knilknrl
locus which drives expression in the L2 primordium. We also propose to
investigate the regulation of a second gene, abrupt (ab), which functions to
organize formation of the L5 vein. In a key experiment, we propose to determine
whether the kni~nrl and ab genes define specific vein types (i.e. L2 versus L5)
or whether they function more generally in promoting vein versus intervein
fates. These studies are of broad medical relevance to understanding the basis
of birth defects. As defects in cell-cell signaling are involved in disease
states such as cancer, the proposed studies also are relevant to such diseases
since development of the L2 vein depends critically on cell-cell communication.
In addition, the TGF-8 related signaling and EGF-R signaling pathways play
prominent roles in maintaining and refining the vein pattern. Because
mis-regulation of these known pathways causes aggressive forms of cancer,
understanding the regulation of these pathways also is of significant relevance
to cancer.
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