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2006 果蝇背腹模式基因
Comprehensive identification of Drosophila
dorsal–ventral patterning genes using
a whole-genome tiling array
´ ´ † † †
Frederic Biemar*, David A. Nix , Jessica Piel*, Brant Peterson*, Matthew Ronshaugen*, Victor Sementchenko , Ian Bell ,
J. Robert Manak†, and Michael S. Levine*‡
*Division of Genetics and Development, Department of Molecular Cell Biology, Center for Integrative Genomics, University of California,
Berkeley, CA 94720; and †Affymetrix, Inc., Santa Clara, CA 95951
Contributed by Michael S. Levine, June 5, 2006
Dorsal–ventral (DV) patterning of the Drosophila embryo is initi- of novel exons. And finally, tiling arrays contain nonprotein
ated by Dorsal, a sequence-specific transcription factor distributed coding genes such as those that specify miRNAs. Indeed, miR-1,
in a broad nuclear gradient in the precellular embryo. Previous a mesoderm-specific miRNA, is directly activated by high levels
studies have identified as many as 70 protein-coding genes and of the gradient in the mesoderm where it influences the activities
one microRNA (miRNA) gene that are directly or indirectly regu- of genes required for the differentiation of the dorsal vessel, the
lated by this gradient. A gene regulation network, or circuit Drosophila heart (3–5). miR-1 expression is regulated by at least
diagram, including the functional interconnections among 40 Dor- two distinct tissue-specific enhancers located in distal and prox-
sal target genes and 20 associated tissue-specific enhancers, has imal regions of the 5 flanking region, respectively. The distal
been determined for the initial stages of gastrulation. Here, we enhancer contains a cluster of linked Dorsa
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