Cited by 317Genomics and Chromatin DynamicsDevelopmental Biology and Gene RegulationGene Regulatory Network Analysis

Regulation of a Segmentation Stripe by Overlapping Activators and Repressors in the Drosophila Embryo

Stanojevic, Dusan, Small, Stephen, Levine, Michael·1991·Science

Abstract

Gene expression stripes in Drosophila melanogaster embryos provide a model for how eukaryotic promoters are turned on and off in response to combinations of transcriptional regulators. Genetic studies suggested that even-skipped ( eve ) stripe 2 is controlled by three gap genes, hunchback ( hb ), Kruppel ( Kr ), and giant ( gt ), and by the maternal morphogen bicoid ( bcd ). A direct link is established between binding sites for these regulatory proteins in the stripe 2 promoter element and the expression of the stripe during early embryogenesis. The bcd and hb protein binding sites mediate activation, whereas neighboring gt and Kr protein sites repress expression and establish the stripe borders. The stripe 2 element has the properties of a genetic on-off switch.

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Crossref · 10.1126/science.1683715

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  • The stripe 2 enhancer controls even-skipped expression in early embryogenesis via binding of tissue-specific transcription factors.

    “The stripe 2 enhancer controls eve expression in early embryogenesis via binding of tissue-specific TFs [121–123].”
  • Activating transcription factors Bicoid and Hunchback are expressed only in the anterior section of the embryo, while repressors Giant and Kruppel are expressed in anterior and posterior regions on either side of stripe 2, such that the stripe 2 enhancer is only activated within a 2-3 cell-wide section of the embryo.

    “Activating TFs Bicoid and Hunchback are expressed only in the anterior section of the embryo, while the repressors Giant and Kruppel are expressed in anterior and posterior regions on either side of stripe 2, such that the stripe 2 enhancer is only activated within a 2–3 cell-wide section of the embryo [108, 121, 124].”

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Authors
Stanojevic, D., Small, S., & Levine, M.
Affiliations
  • Department of Biological Sciences, Fairchild Center, Columbia University, New York, NY 10027.
  • University of California System (US)
Venue
Science
Published
1991-11-29
Volume
254
Issue
5036
Pages
1385-1387
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2048066878
Cited by
317
References
1
Citations by year
2026: 1 · 2025: 6 · 2024: 5 · 2023: 8 · 2022: 7 · 2021: 4 · 2020: 5 · 2019: 5 · 2018: 12 · 2017: 12 · 2016: 11 · 2015: 10 · 2014: 6 · 2013: 12 · 2012: 9
FWCI
6.34
Type
journal article
Language
en
Open access
closed
Locations
  • Science (publishedVersion)
  • PubMed (publishedVersion)
Funders
National Institute of General Medical Sciences (R01GM034431, GM34431)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene Regulatory Network Analysis
Keywords
Drosophila melanogaster embryo, gap genes, hunchback, Krüppel, giants, Bicoid, transcriptional regulation, promoter binding sites, on-off switch, embryonic segmentation
MeSH terms
Animals, Base Sequence, Chromosome Deletion, Drosophila melanogaster, Embryo, Nonmammalian, Gene Expression Regulation, Genes, Genes, Homeobox, Molecular Sequence Data, Morphogenesis, Oligodeoxyribonucleotides, Promoter Regions, Genetic, Mutagenesis, Site-Directed

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