| Literature DB >> 32726635 |
Jianli Duan1, Yunpo Zhao2, Haichao Li3, Lukas Habernig4, Michael D Gordon5, Xuexia Miao3, Ylva Engström4, Sabrina Büttner6.
Abstract
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-à-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.Entities:
Keywords: Bab2; Broad; Drosophila; EcR/USP; Sgs genes; ecdysone; glue genes; salivary gland; steroid hormone; transcriptional regulation
Mesh:
Substances:
Year: 2020 PMID: 32726635 DOI: 10.1016/j.celrep.2020.107972
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423