» Articles » PMID: 34634038

Metabolic Gene Regulation by Drosophila GATA Transcription Factor Grain

Overview
Journal PLoS Genet
Specialty Genetics
Date 2021 Oct 11
PMID 34634038
Authors
Affiliations
Soon will be listed here.
Abstract

Nutrient-dependent gene regulation critically contributes to homeostatic control of animal physiology in changing nutrient landscape. In Drosophila, dietary sugars activate transcription factors (TFs), such as Mondo-Mlx, Sugarbabe and Cabut, which control metabolic gene expression to mediate physiological adaptation to high sugar diet. TFs that correspondingly control sugar responsive metabolic genes under conditions of low dietary sugar remain, however, poorly understood. Here we identify a role for Drosophila GATA TF Grain in metabolic gene regulation under both low and high sugar conditions. De novo motif prediction uncovered a significant over-representation of GATA-like motifs on the promoters of sugar-activated genes in Drosophila larvae, which are regulated by Grain, the fly ortholog of GATA1/2/3 subfamily. grain expression is activated by sugar in Mondo-Mlx-dependent manner and it contributes to sugar-responsive gene expression in the fat body. On the other hand, grain displays strong constitutive expression in the anterior midgut, where it drives lipogenic gene expression also under low sugar conditions. Consistently with these differential tissue-specific roles, Grain deficient larvae display delayed development on high sugar diet, while showing deregulated central carbon and lipid metabolism primarily on low sugar diet. Collectively, our study provides evidence for the role of a metazoan GATA transcription factor in nutrient-responsive metabolic gene regulation in vivo.

References
1.
Tennessen J, Barry W, Cox J, Thummel C . Methods for studying metabolism in Drosophila. Methods. 2014; 68(1):105-15. PMC: 4048761. DOI: 10.1016/j.ymeth.2014.02.034. View

2.
Li H, Chawla G, Hurlburt A, Sterrett M, Zaslaver O, Cox J . Drosophila larvae synthesize the putative oncometabolite L-2-hydroxyglutarate during normal developmental growth. Proc Natl Acad Sci U S A. 2017; 114(6):1353-1358. PMC: 5307464. DOI: 10.1073/pnas.1614102114. View

3.
Landt S, Marinov G, Kundaje A, Kheradpour P, Pauli F, Batzoglou S . ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia. Genome Res. 2012; 22(9):1813-31. PMC: 3431496. DOI: 10.1101/gr.136184.111. View

4.
Bailey T . DREME: motif discovery in transcription factor ChIP-seq data. Bioinformatics. 2011; 27(12):1653-9. PMC: 3106199. DOI: 10.1093/bioinformatics/btr261. View

5.
Loewith R, Hall M . Target of rapamycin (TOR) in nutrient signaling and growth control. Genetics. 2011; 189(4):1177-201. PMC: 3241408. DOI: 10.1534/genetics.111.133363. View