Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Bab2 Functions as an Ecdysone-Responsive Transcriptional Repressor during Drosophila Development
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute. Chinese Academy of Sciences, China.
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute. Chinese Academy of Sciences, China; University of British Columbia, Canada.ORCID iD: 0000-0002-7942-3406
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.
Show others and affiliations
Number of Authors: 82020 (English)In: Cell Reports, E-ISSN 2211-1247, Vol. 32, no 4, article id 107972Article in journal (Refereed) Published
Abstract [en]

Drosophila development is governed by distinct ecdysone steroid pulses that initiate spatially and temporally defined gene expression programs. The translation of these signals into tissue-specific responses is crucial for metamorphosis, but the mechanisms that confer specificity to systemic ecdysone pulses are far from understood. Here, we identify Bric-a-brac 2 (Bab2) as an ecdysone-responsive transcriptional repressor that controls temporal gene expression during larval to pupal transition. Bab2 is necessary to terminate Salivary gland secretion (Sgs) gene expression, while premature Bab2 expression blocks Sgs genes and causes precocious salivary gland histolysis. The timely expression of bab2 is controlled by the ecdysone-responsive transcription factor Broad, and manipulation of EcR/USP/Broad signaling induces inappropriate Bab2 expression and termination of Sgs gene expression. Bab2 directly binds to Sgs loci in vitro and represses all Sgs genes in vivo. Our work characterizes Bab2 as a temporal regulator of somatic gene expression in response to systemic ecdysone signaling.

Place, publisher, year, edition, pages
2020. Vol. 32, no 4, article id 107972
National Category
Biological Sciences
Identifiers
URN: urn:nbn:se:su:diva-185457DOI: 10.1016/j.celrep.2020.107972ISI: 000555895400007PubMedID: 32726635OAI: oai:DiVA.org:su-185457DiVA, id: diva2:1474941
Available from: 2020-10-11 Created: 2020-10-11 Last updated: 2024-01-17Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMed

Authority records

Duan, JianliZhao, YunpoHabernig, LukasGordon, Michael D.Engström, YlvaBüttner, Sabrina

Search in DiVA

By author/editor
Duan, JianliZhao, YunpoHabernig, LukasGordon, Michael D.Engström, YlvaBüttner, Sabrina
By organisation
Department of Molecular Biosciences, The Wenner-Gren Institute
In the same journal
Cell Reports
Biological Sciences

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 112 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf