Cited by 349Developmental Biology and Gene RegulationGenomics and Chromatin DynamicsRNA Research and Splicing

Transcriptional regulation of a pair-rule stripe in Drosophila.

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Small, S, Kraut, R, Hoey, T, Warrior, R, Levine, M·1991·Genes & Development

Abstract

The periodic, seven-stripe pattern of the primary pair-rule gene even-skipped (eve) is initiated by crude, overlapping gradients of maternal and gap gene proteins in the early Drosophila embryo. Previous genetic studies suggest that one of the stripes, stripe 2, is initiated by the maternal morphogen bicoid (bcd) and the gap protein hunchback (hb), while the borders of the stripe are formed by selective repression, involving the gap protein giant (gt) in anterior regions and the Krüppel (Kr) protein in posterior regions. Here, we present several lines of evidence that are consistent with this model for stripe 2 expression, including in vitro DNA-binding experiments and transient cotransfection assays in cultured cells. These experiments suggest that repression involves a competition or short-range quenching mechanism, whereby the binding of gt and Kr interferes with the binding or activity of bcd and hb activators at overlapping or neighboring sites within the eve stripe 2 promoter element. Such short-range repression could reflect a general property of promoters composed of multiple, but autonomous regulatory elements.

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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].”

    From Transcriptional enhancers and their communication with gene promoters (2021) · cites this paper as [123]

    The Abstract and Discussion describe the stripe 2 regulatory element as binding factors that activate or repress eve expression in early embryos. They identify these factors as a maternal morphogen and gap proteins with spatially patterned expression, but do not establish that they are tissue-specific transcription factors. (LLM, conf=0.82)

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Research works printed but not linked: 2

  1. Kadonaga, J.T. and R. Tjian. 1986. Affinity purification of se- quence-specific DNA binding proteins. Proc. Natl. Acad. Sci. 83: 5889-5893.
  2. Rhodes, D. and A. Klug. 1988. Zinc fingers: A novel motif for nucleic acid binding. In Nucleic acids and molecuIar biol- ogy. (ed. F. Ecksteinn, and D.J.M. Lilley), vol. 2. Springer- Verlag, Berlin.

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Authors
Small, S., Kraut, R., Hoey, T., Warrior, R., & Levine, M.
Affiliations
  • Columbia University (US)
  • University of California San Diego (US)
  • F. Hoffmann-La Roche AG (CH)
Venue
Genes & Development
Published
1991-05
Volume
5
Issue
5
Pages
827-839
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W2064171951
Cited by
349
References
1
Citations by year
2026: 2 · 2025: 5 · 2024: 4 · 2023: 10 · 2022: 5 · 2021: 12 · 2020: 5 · 2019: 10 · 2018: 10 · 2017: 10 · 2016: 11 · 2015: 5 · 2014: 5 · 2013: 9 · 2012: 5
Type
posted content
Language
en
Open access
Locations
  • Genes & Development (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health
  • National Institute of General Medical Sciences (R01GM034431, GM34431)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
Keywords
even-skipped, transcriptional repression, Bicoid, hunchback, giants, Krüppel, gap genes, promoter elements, Drosophila embryo, gene expression patterning
MeSH terms
Amino Acid Sequence, Animals, Bacterial Proteins, Base Sequence, Cells, Cultured, DNA, DNA-Binding Proteins, Drosophila, Gene Expression Regulation, Insect Hormones, Juvenile Hormones, Molecular Sequence Data, Phenotype, Promoter Regions, Genetic, Repressor Proteins, Transcription Factors, Transcription, Genetic, Transfection, Trans-Activators, Homeodomain Proteins, Drosophila Proteins, Kruppel-Like Transcription Factors

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